Variant report

Variant	rs2393667
Chromosome Location	chr6:26421345-26421346
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	CREB1	chr6:26421323-26421820	ECC-1	luminal epithelium:	n/a	n/a
2	POLR2A	chr6:26420638-26422563	H1-hESC	embryonic stem cell:	n/a	n/a
3	RFX5	chr6:26420705-26422190	H1-hESC	embryonic stem cell:	n/a	chr6:26421550-26421558
4	MAX	chr6:26421300-26422067	Hela-S3	cervix:	n/a	n/a
5	SIN3A	chr6:26420955-26421356	H1-hESC	embryonic stem cell:	n/a	n/a
6	SMC3	chr6:26420816-26421950	Hela-S3	cervix:	n/a	chr6:26420986-26421000
7	NFYA	chr6:26421333-26421919	K562	blood:	n/a	n/a
8	RFX5	chr6:26420811-26422070	HepG2	liver:	n/a	chr6:26421550-26421558
9	CTCF	chr6:26421200-26421350	GM06990	blood:	n/a	n/a
10	SP4	chr6:26420861-26421398	H1-hESC	embryonic stem cell:	n/a	n/a
11	MYBL2	chr6:26420765-26422133	HepG2	liver:	n/a	n/a
12	RFX5	chr6:26420813-26422131	Hela-S3	cervix:	n/a	chr6:26421550-26421558
13	TAF1	chr6:26420843-26422528	H1-hESC	embryonic stem cell:	n/a	n/a
14	SMC3	chr6:26420637-26422211	SK-N-SH	brain:	n/a	chr6:26420986-26421000
15	CREB1	chr6:26421141-26421932	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr6:26420775-26422133	HepG2	liver:	n/a	n/a
17	CREB1	chr6:26421335-26422025	GM12878	blood:	n/a	n/a
18	CREB1	chr6:26421301-26421818	ECC-1	luminal epithelium:	n/a	n/a
19	CTCF	chr6:26421260-26421410	NB4	blood:	n/a	n/a
20	ZNF263	chr6:26420888-26422615	HEK293-T-REx	kidney:	n/a	chr6:26422032-26422041 chr6:26422017-26422038 chr6:26422016-26422025
21	RFX5	chr6:26419671-26423665	IMR90	lung:	n/a	chr6:26421550-26421558
22	POLR2A	chr6:26421015-26422439	SK-N-MC	brain:	n/a	n/a
23	KAP1	chr6:26420774-26421931	HEK293	kidney:	n/a	chr6:26421350-26421358
24	CTCF	chr6:26421300-26421450	AG10803	skin:	n/a	n/a
25	TAF1	chr6:26421199-26421383	SK-N-SH	brain:	n/a	n/a
26	CTCF	chr6:26421220-26421370	RPTEC	kidney:	n/a	n/a
27	POLR2A	chr6:26421310-26422191	HUVEC	blood vessel:	n/a	n/a
28	MXI1	chr6:26421315-26421813	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr6:26421200-26421350	GM12873	blood:	n/a	n/a
30	CTCF	chr6:26421200-26421350	GM12878	blood:	n/a	n/a
31	CHD2	chr6:26421185-26421917	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr6:26420807-26422027	GM12878	blood:	n/a	n/a
33	CREB1	chr6:26421190-26422031	HepG2	liver:	n/a	n/a
34	CTCF	chr6:26421200-26421350	BJ	skin:	n/a	n/a
35	TEAD4	chr6:26420766-26421926	HepG2	liver:	n/a	n/a
36	MYBL2	chr6:26420798-26422074	HepG2	liver:	n/a	n/a
37	RFX5	chr6:26419605-26423677	SK-N-SH	brain:	n/a	chr6:26421550-26421558
38	GTF2F1	chr6:26421106-26421390	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr6:26421283-26421458	H1-hESC	embryonic stem cell:	n/a	n/a
40	RFX5	chr6:26420818-26422133	K562	blood:	n/a	chr6:26421550-26421558
41	CREB1	chr6:26421173-26422033	K562	blood:	n/a	n/a
42	SP1	chr6:26421332-26421830	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:26421220-26421370	BE2_C	brain:	n/a	n/a
44	TEAD4	chr6:26421195-26422210	K562	blood:	n/a	chr6:26422149-26422158
45	CTCF	chr6:26421260-26421410	HMEC	breast:	n/a	n/a
46	POLR2A	chr6:26420939-26421453	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr6:26421174-26422303	PFSK-1	brain:	n/a	n/a
48	NR2F2	chr6:26421209-26422228	K562	blood:	n/a	n/a
49	JUN	chr6:26421334-26421656	K562	blood:	n/a	chr6:26421473-26421482
50	CTCF	chr6:26420788-26421546	SK-N-SH	brain:	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:

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

Extended variants
information (count: 141 )
Associated
traits (count: 20 )

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs10484443	0.89[CHB][hapmap]
rs12173854	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12174602	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12174623	0.87[EUR][1000 genomes]
rs12174631	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12174639	0.87[EUR][1000 genomes]
rs12176129	0.89[EUR][1000 genomes]
rs12176317	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs13191660	0.87[EUR][1000 genomes]
rs13195509	0.92[CEU][hapmap]
rs13198716	1.00[YRI][hapmap]
rs13214027	0.85[CEU][hapmap]
rs13216828	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs13220261	0.91[CEU][hapmap]
rs13220495	1.00[YRI][hapmap];0.81[AMR][1000 genomes]
rs13220522	0.81[AMR][1000 genomes]
rs16891725	1.00[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap];0.92[EUR][1000 genomes]
rs16901784	0.86[CEU][hapmap];0.89[CHB][hapmap];0.82[EUR][1000 genomes]
rs1977	1.00[CEU][hapmap];0.92[JPT][hapmap];0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs1978	1.00[CEU][hapmap];0.92[JPT][hapmap];0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs1979	1.00[CEU][hapmap];0.93[JPT][hapmap];0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs2072803	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2072806	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2073527	0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs2073529	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs2073530	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs2073531	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs2076030	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2093169	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs2235251	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2295593	0.89[EUR][1000 genomes]
rs2393593	1.00[YRI][hapmap]
rs28362606	0.86[EUR][1000 genomes]
rs28551159	0.87[EUR][1000 genomes]
rs3047288	0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs34107459	0.81[AMR][1000 genomes]
rs34273322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34436535	0.87[EUR][1000 genomes]
rs34550936	0.87[EUR][1000 genomes]
rs34622023	0.87[EUR][1000 genomes]
rs34878490	0.87[EUR][1000 genomes]
rs35304979	0.87[EUR][1000 genomes]
rs35307327	0.87[EUR][1000 genomes]
rs35934643	0.87[EUR][1000 genomes]
rs35942482	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3734542	0.91[CEU][hapmap]
rs3734544	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs3757138	0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs3757150	0.81[CEU][hapmap];0.89[CHB][hapmap]
rs3799378	0.84[JPT][hapmap]
rs3799380	0.85[CEU][hapmap]
rs3799383	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap];0.89[EUR][1000 genomes]
rs3823158	0.92[CEU][hapmap]
rs41266839	0.81[AMR][1000 genomes]
rs55706012	0.81[AMR][1000 genomes]
rs6456728	0.85[CEU][hapmap]
rs66823108	0.84[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs67234939	0.89[EUR][1000 genomes]
rs67509210	0.87[EUR][1000 genomes]
rs68072215	0.84[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs6900665	0.86[EUR][1000 genomes]
rs6911765	0.89[CHB][hapmap]
rs6920256	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap];0.84[EUR][1000 genomes]
rs71544290	0.87[EUR][1000 genomes]
rs71557332	0.85[EUR][1000 genomes]
rs71557334	0.87[EUR][1000 genomes]
rs71557335	0.87[EUR][1000 genomes]
rs72836482	0.87[EUR][1000 genomes]
rs72841536	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs7773938	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs9348709	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9348712	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9348716	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9348718	0.89[CHB][hapmap]
rs9348721	0.86[EUR][1000 genomes]
rs9357006	0.87[EUR][1000 genomes]
rs9358930	0.87[EUR][1000 genomes]
rs9358932	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9358934	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9358935	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9358937	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9358938	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9358939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9358944	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs9358945	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs9358946	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs9366653	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9366654	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9366655	0.92[CEU][hapmap];0.93[JPT][hapmap];0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs9366656	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9366658	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs9379851	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9379852	0.87[EUR][1000 genomes]
rs9379853	0.87[EUR][1000 genomes]
rs9379854	0.87[EUR][1000 genomes]
rs9379855	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9379856	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9379857	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9379858	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9379859	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9379863	0.87[EUR][1000 genomes]
rs9379864	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs9379871	0.87[EUR][1000 genomes]
rs9379873	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9379875	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9379882	0.89[EUR][1000 genomes]
rs9393703	0.87[EUR][1000 genomes]
rs9393704	0.87[EUR][1000 genomes]
rs9393705	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9393706	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9393707	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9393708	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9393710	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9393711	0.87[EUR][1000 genomes]
rs9393712	0.87[EUR][1000 genomes]
rs9393713	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9393714	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs9393715	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs9393718	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9393721	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs9393727	0.89[EUR][1000 genomes]
rs9393735	0.93[CEU][hapmap];0.85[JPT][hapmap]
rs9467772	0.81[CEU][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:20)

SNP	Gene	Cis/trans	Tissue	Source
rs2393667	BTN3A2	cis	Whole Blood	GTEx
rs2393667	BTN3A2	cis	Stomach	GTEx
rs2393667	BTN3A2	Cis_1M	lymphoblastoid	RTeQTL
rs2393667	BTN3A2	cis	uninvolved skin	skin_eQTL
rs2393667	BTN3A2	cis	Muscle Skeletal	GTEx
rs2393667	BTN3A2	cis	Esophagus Muscularis	GTEx
rs2393667	BTN3A2	cis	Thyroid	GTEx
rs2393667	BTN3A2	cis	Adipose Subcutaneous	GTEx
rs2393667	BTN3A2	cis	lung	GTEx
rs2393667	BTN3A2	cis	Heart Left Ventricle	GTEx
rs2393667	BTN3A2///BTN3A3	Cis_1M	lymphoblastoid	RTeQTL
rs2393667	BTN3A2	cis	Skin Sun Exposed Lower leg	GTEx
rs2393667	BTN3A1	Cis_1M	lymphoblastoid	RTeQTL
rs2393667	BTN3A2	cis	Artery Aorta	GTEx
rs2393667	BTN3A2	cis	Esophagus Mucosa	GTEx
rs2393667	BTN3A2	cis	lesional skin	skin_eQTL
rs2393667	BTN3A2	cis	normal skin	skin_eQTL
rs2393667	BTN3A2	cis	multi-tissue	Pritchard
rs2393667	BTN3A2	cis	Artery Tibial	GTEx
rs2393667	BTN3A2	cis	Nerve Tibial	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26413600-26421600	Weak transcription	Gastric	stomach
2	chr6:26414800-26421600	Weak transcription	Lung	lung
3	chr6:26420200-26421400	Enhancers	Spleen	Spleen
4	chr6:26420400-26421800	Active TSS	Fetal Brain Male	brain
5	chr6:26420800-26422600	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr6:26421000-26421400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
7	chr6:26421000-26421400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:26421000-26421400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:26421000-26421400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:26421000-26421400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr6:26421000-26421400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr6:26421000-26421400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr6:26421000-26421400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:26421000-26421400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:26421000-26421400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:26421000-26421400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr6:26421000-26421400	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr6:26421000-26421400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr6:26421000-26421400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:26421000-26421400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr6:26421000-26421400	Flanking Active TSS	Brain Cingulate Gyrus	brain
22	chr6:26421000-26421400	Flanking Active TSS	Brain Hippocampus Middle	brain
23	chr6:26421000-26421400	Flanking Active TSS	Colon Smooth Muscle	Colon
24	chr6:26421000-26421400	Flanking Active TSS	Fetal Kidney	kidney
25	chr6:26421000-26421400	Flanking Active TSS	Fetal Lung	lung
26	chr6:26421000-26421400	Flanking Active TSS	Fetal Muscle Leg	muscle
27	chr6:26421000-26421400	Enhancers	Placenta Amnion	Placenta Amnion
28	chr6:26421000-26421400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr6:26421000-26421400	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr6:26421000-26421400	Flanking Active TSS	HSMM	muscle
31	chr6:26421000-26421400	Flanking Active TSS	HUVEC	blood vessel
32	chr6:26421000-26421400	Flanking Active TSS	NHDF-Ad	bronchial
33	chr6:26421000-26421600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:26421000-26421600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr6:26421000-26421600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr6:26421000-26421600	Flanking Active TSS	Primary hematopoietic stem cells	blood
37	chr6:26421000-26421600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr6:26421000-26421600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr6:26421000-26421600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr6:26421000-26421600	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr6:26421000-26421600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr6:26421000-26421600	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr6:26421000-26421600	Flanking Active TSS	Dnd41	blood
44	chr6:26421000-26421600	Flanking Active TSS	GM12878-XiMat	blood
45	chr6:26421000-26421600	Flanking Active TSS	Hela-S3	cervix
46	chr6:26421000-26421600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr6:26421000-26421600	Flanking Active TSS	Osteobl	bone
48	chr6:26421000-26421800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr6:26421000-26422200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr6:26421000-26422200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood

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