Variant report

Variant	rs7744254
Chromosome Location	chr6:26421030-26421031
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:26420920-26421070	HVMF	connective:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
2	CTCF	chr6:26420867-26421122	K562	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
3	CTCF	chr6:26420920-26421070	HCFaa	heart:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
4	POLR2A	chr6:26420638-26422563	H1-hESC	embryonic stem cell:	n/a	n/a
5	RAD21	chr6:26420732-26421252	H1-hESC	embryonic stem cell:	n/a	chr6:26420982-26421001 chr6:26420986-26421000
6	CTCF	chr6:26420920-26421070	GM12865	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
7	RFX5	chr6:26420705-26422190	H1-hESC	embryonic stem cell:	n/a	chr6:26421550-26421558
8	CTCF	chr6:26420920-26421070	AG04449	skin:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
9	CTCF	chr6:26420889-26421136	K562	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
10	CTCF	chr6:26420879-26421156	Spleen_OC	spleen:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
11	CTCF	chr6:26420900-26421050	AG04450	lung:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
12	CTCF	chr6:26420889-26421114	Gliobla	brain:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
13	CTCF	chr6:26420952-26421088	Pancreas_OC	pancreas:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
14	E2F6	chr6:26420737-26421178	H1-hESC	embryonic stem cell:	n/a	chr6:26420773-26420782
15	CTCF	chr6:26420900-26421050	HAc	cerebellar:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
16	CTCF	chr6:26420980-26421130	HFF-Myc	foreskin:	n/a	chr6:26420986-26420999 chr6:26420984-26421002
17	CTCF	chr6:26420940-26421090	AG09309	skin:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
18	SMC3	chr6:26420815-26421196	HepG2	liver:	n/a	chr6:26420986-26421000
19	CTCF	chr6:26420900-26421050	GM12867	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
20	CTCF	chr6:26420940-26421090	HPF	lung:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
21	RAD21	chr6:26420799-26421131	MCF-7	breast:	n/a	chr6:26420982-26421001 chr6:26420986-26421000
22	SIN3A	chr6:26420955-26421356	H1-hESC	embryonic stem cell:	n/a	n/a
23	RAD21	chr6:26420779-26421148	H1-hESC	embryonic stem cell:	n/a	chr6:26420982-26421001 chr6:26420986-26421000
24	SMC3	chr6:26420816-26421950	Hela-S3	cervix:	n/a	chr6:26420986-26421000
25	CTCF	chr6:26420880-26421030	NHEK	skin:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
26	POLR2A	chr6:26420989-26421129	H1-hESC	embryonic stem cell:	n/a	n/a
27	RAD21	chr6:26420842-26421174	IMR90	lung:	n/a	chr6:26420982-26421001 chr6:26420986-26421000
28	CTCF	chr6:26420900-26421050	HMF	breast:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
29	CTCF	chr6:26420920-26421070	SK-N-SH_RA	brain:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
30	CTCF	chr6:26420960-26421110	GM12869	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
31	ATF1	chr6:26420969-26421083	K562	blood:	n/a	n/a
32	CTCF	chr6:26420944-26421084	LNCaP	prostate:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
33	RAD21	chr6:26420725-26421334	HCT-116	colon:	n/a	chr6:26420982-26421001 chr6:26420986-26421000
34	CTCF	chr6:26420830-26421220	H1-hESC	embryonic stem cell:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
35	RFX5	chr6:26420811-26422070	HepG2	liver:	n/a	chr6:26421550-26421558
36	CTCF	chr6:26420880-26421030	GM06990	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
37	CTCF	chr6:26420980-26421130	WI-38	lung:	n/a	chr6:26420986-26420999 chr6:26420984-26421002
38	CTCF	chr6:26420880-26421030	MCF-7	breast:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
39	SP4	chr6:26420861-26421398	H1-hESC	embryonic stem cell:	n/a	n/a
40	MYBL2	chr6:26420765-26422133	HepG2	liver:	n/a	n/a
41	CTCF	chr6:26420920-26421070	GM12868	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
42	CTCF	chr6:26420960-26421110	HCM	heart:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
43	CTCF	chr6:26420880-26421030	HCT-116	colon:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
44	CTCF	chr6:26420936-26421077	GM13976	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
45	RFX5	chr6:26420813-26422131	Hela-S3	cervix:	n/a	chr6:26421550-26421558
46	TAF1	chr6:26420843-26422528	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr6:26420920-26421070	AG09309	skin:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
48	SMC3	chr6:26420637-26422211	SK-N-SH	brain:	n/a	chr6:26420986-26421000
49	CTCF	chr6:26420940-26421090	GM12871	blood:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002
50	CTCF	chr6:26420900-26421050	Caco-2	colon:	n/a	chr6:26420979-26421000 chr6:26420986-26420999 chr6:26420984-26421002

No.	Distal block	Cell Line	Cell type
1	chr6:26341882..26342492-chr6:26420774..26421520,2	MCF-7	breast:
2	chr6:26419843..26421610-chr6:26453709..26456222,2	K562	blood:
3	chr6:26384982..26386521-chr6:26418535..26421413,2	K562	blood:
4	chr6:26193666..26195814-chr6:26420014..26422966,2	K562	blood:
5	chr6:26420245..26422646-chr6:26519763..26522632,2	K562	blood:
6	chr6:26420252..26422779-chr6:26519711..26522673,2	K562	blood:
7	chr6:26196016..26198386-chr6:26419404..26421954,3	K562	blood:
8	chr6:26419994..26421593-chr6:26434253..26437135,2	K562	blood:
9	chr6:26383587..26385903-chr6:26419597..26421640,2	MCF-7	breast:
10	chr6:26414624..26416955-chr6:26417955..26421262,4	K562	blood:

Variant related genes	Relation type
BTN2A3P	TF binding region
ENSG00000197409	Chromatin interaction
ENSG00000216331	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000124508	Chromatin interaction

Extended variants
information (count: 159 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:141)

rs_ID	r²[population]
rs10447390	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10447391	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10456047	0.86[CEU][hapmap]
rs10456331	0.86[CEU][hapmap]
rs10484441	0.86[CEU][hapmap]
rs10807008	0.91[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs10946820	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946823	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946824	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946825	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946826	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946828	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946829	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946830	1.00[ASN][1000 genomes]
rs10946832	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12191917	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12193283	0.86[CEU][hapmap]
rs12194001	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12194036	0.86[CEU][hapmap]
rs12194073	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12194412	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12196371	0.86[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12198993	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12201546	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12203108	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12203120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12203176	1.00[CHD][hapmap]
rs12205476	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs12206812	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12206839	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12207930	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12208211	0.86[CEU][hapmap]
rs12208329	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12211872	0.86[CEU][hapmap]
rs12213625	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12214444	0.92[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[MEX][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12214486	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12214924	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12214976	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12661560	0.86[CEU][hapmap]
rs12662604	1.00[ASN][1000 genomes]
rs12664899	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs17537465	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs17539219	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17610161	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs17611220	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17611438	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap]
rs1884945	0.86[CEU][hapmap]
rs2393652	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2393655	0.93[CEU][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2393656	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2393664	0.80[CEU][hapmap]
rs28571747	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2893844	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2893845	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2893846	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2893847	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2893848	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2893849	0.93[CEU][hapmap]
rs2893856	0.93[CEU][hapmap]
rs2893857	0.86[CEU][hapmap]
rs3198487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3208734	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34268421	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3807025	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3846843	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3846844	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3846847	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3846848	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3846849	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3902051	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[YRI][hapmap];1.00[ASN][1000 genomes]
rs3903661	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4083469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4305717	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45499696	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4609015	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4711108	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4711109	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4711110	0.85[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4711111	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712988	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[YRI][hapmap]
rs4712989	1.00[ASN][1000 genomes]
rs4712990	0.91[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[MEX][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4712992	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712993	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712994	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712995	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712996	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712999	0.93[CEU][hapmap]
rs4713000	0.85[CEU][hapmap]
rs4713001	0.86[CEU][hapmap]
rs55775018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55786210	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55957716	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55994013	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56023587	1.00[ASN][1000 genomes]
rs56139485	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56143200	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56157336	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56161420	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56182232	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56190518	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56207464	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56280732	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56325223	1.00[ASN][1000 genomes]
rs57275245	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60750900	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6456716	1.00[CHD][hapmap]
rs6456721	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6456722	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6456723	0.86[CEU][hapmap]
rs6456724	0.93[CEU][hapmap]
rs6900725	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6901245	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6910023	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6912934	0.93[CEU][hapmap]
rs6920986	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6926878	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6928454	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929846	0.86[CEU][hapmap]
rs6931648	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72841540	0.84[ASN][1000 genomes]
rs7356982	0.87[CEU][hapmap]
rs7745238	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7745767	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7751280	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7754940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7755398	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7768108	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs7770214	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7770699	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7775365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs882010	0.86[CEU][hapmap]
rs9104	1.00[CHD][hapmap]
rs9295690	0.80[CEU][hapmap]
rs9461245	1.00[CHD][hapmap]
rs9467748	0.80[CEU][hapmap]
rs9467759	0.93[CEU][hapmap]
rs9688949	1.00[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
4	nsv482729	chr6:26291011-26470898	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv482836	chr6:26352883-26520964	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv883492	chr6:26367689-26436592	Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv883493	chr6:26367689-26442786	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
8	nsv883494	chr6:26367833-26442786	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
9	nsv883495	chr6:26367833-26443853	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
10	esv3334611	chr6:26367893-26443308	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	nsv482407	chr6:26369320-26550148	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
12	nsv883497	chr6:26369549-26442786	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv883498	chr6:26369549-26443853	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv883499	chr6:26377591-26454454	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
15	esv3427999	chr6:26378373-26453532	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
16	nsv462664	chr6:26379537-26451553	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
17	nsv601184	chr6:26379537-26451553	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
18	nsv969358	chr6:26420389-26423517	Genic enhancers Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs7744254	BTN2A1	cis	parietal	SCAN
rs7744254	BTN2A2	Cis_1M	lymphoblastoid	RTeQTL
rs7744254	BTN2A3P	cis	Esophagus Muscularis	GTEx
rs7744254	BTN2A1	cis	cerebellum	SCAN
rs7744254	HIST1H3H	cis	cerebellum	SCAN
rs7744254	BTN2A3P	cis	Artery Tibial	GTEx
rs7744254	BTN3A1	Cis_1M	lymphoblastoid	RTeQTL
rs7744254	BTN3A3	cis	cerebellum	SCAN
rs7744254	BTN2A2	cis	cerebellum	SCAN
rs7744254	BTN3A1	cis	cerebellum	SCAN

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26403000-26421200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:26403000-26421200	Weak transcription	Right Ventricle	heart
3	chr6:26403600-26421200	Weak transcription	Psoas Muscle	Psoas
4	chr6:26405800-26421200	Weak transcription	Small Intestine	intestine
5	chr6:26413600-26421600	Weak transcription	Gastric	stomach
6	chr6:26414000-26421200	Weak transcription	Left Ventricle	heart
7	chr6:26414800-26421200	Weak transcription	Thymus	Thymus
8	chr6:26414800-26421600	Weak transcription	Lung	lung
9	chr6:26420200-26421200	Enhancers	Primary T cells fromperipheralblood	blood
10	chr6:26420200-26421200	Enhancers	Fetal Stomach	stomach
11	chr6:26420200-26421200	Enhancers	HSMMtube	muscle
12	chr6:26420200-26421200	Enhancers	K562	blood
13	chr6:26420200-26421400	Enhancers	Spleen	Spleen
14	chr6:26420400-26421200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:26420400-26421200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:26420400-26421200	Enhancers	Fetal Heart	heart
17	chr6:26420400-26421800	Active TSS	Fetal Brain Male	brain
18	chr6:26420600-26421200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:26420600-26421200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr6:26420600-26421200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr6:26420600-26421200	Enhancers	Liver	Liver
22	chr6:26420600-26421200	Enhancers	Fetal Muscle Trunk	muscle
23	chr6:26420800-26421200	Enhancers	Primary B cells from peripheral blood	blood
24	chr6:26420800-26421200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr6:26420800-26421200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr6:26420800-26421200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr6:26420800-26421200	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr6:26420800-26421200	Enhancers	Brain Germinal Matrix	brain
29	chr6:26420800-26421200	Enhancers	Pancreas	Pancrea
30	chr6:26420800-26421200	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr6:26420800-26421200	Enhancers	A549	lung
32	chr6:26420800-26421200	Flanking Active TSS	HepG2	liver
33	chr6:26420800-26421200	Enhancers	NH-A	brain
34	chr6:26420800-26421200	Enhancers	NHEK	skin
35	chr6:26420800-26421200	Enhancers	NHLF	lung
36	chr6:26420800-26422600	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr6:26421000-26421200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:26421000-26421200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:26421000-26421200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:26421000-26421200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr6:26421000-26421200	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr6:26421000-26421200	Enhancers	Primary T cells from cord blood	blood
43	chr6:26421000-26421200	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr6:26421000-26421200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr6:26421000-26421200	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr6:26421000-26421200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr6:26421000-26421200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr6:26421000-26421200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:26421000-26421200	Flanking Active TSS	Aorta	Aorta
50	chr6:26421000-26421200	Enhancers	Brain Angular Gyrus	brain

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