Variant report

Variant	rs3131034
Chromosome Location	chr6:30853796-30853797
allele	A/G
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	SIN3A	chr6:30851614-30854616	H1-hESC	embryonic stem cell:	n/a	chr6:30854237-30854248
2	FOXA2	chr6:30853203-30854330	A549	lung:	n/a	n/a
3	CEBPB	chr6:30853611-30854337	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr6:30853447-30854073	MCF-7	breast:	n/a	n/a
5	FOSL2	chr6:30853421-30854410	SK-N-SH	brain:	n/a	chr6:30854029-30854036 chr6:30854029-30854038 chr6:30854028-30854038 chr6:30854026-30854037 chr6:30854029-30854037 chr6:30854027-30854039 chr6:30854028-30854037
6	RAD21	chr6:30853752-30854178	SK-N-SH_RA	brain:	n/a	n/a
7	TAF1	chr6:30853622-30854764	H1-neurons	neurons:	n/a	n/a
8	POLR2A	chr6:30853756-30854557	H1-hESC	embryonic stem cell:	n/a	n/a
9	TAF1	chr6:30853735-30854668	H1-neurons	neurons:	n/a	n/a
10	USF2	chr6:30853778-30854111	Hela-S3	cervix:	n/a	n/a
11	SP1	chr6:30853747-30854599	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr6:30853433-30854090	HepG2	liver:	n/a	n/a
13	POLR2A	chr6:30853747-30854017	A549	lung:	n/a	n/a
14	RCOR1	chr6:30853577-30854527	K562	blood:	n/a	n/a
15	POLR2A	chr6:30853723-30854232	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr6:30853795-30854035	MCF10A-Er-Src	breast:	n/a	n/a
17	JUND	chr6:30852577-30854836	SK-N-SH	brain:	n/a	chr6:30854029-30854036 chr6:30852804-30852814 chr6:30852801-30852812 chr6:30854029-30854038 chr6:30852804-30852814 chr6:30854027-30854038 chr6:30852632-30852641 chr6:30852804-30852814 chr6:30854028-30854038 chr6:30854029-30854037 chr6:30854027-30854039 chr6:30854028-30854037 chr6:30852804-30852814
18	MYBL2	chr6:30853640-30854221	HepG2	liver:	n/a	n/a
19	FOSL1	chr6:30853773-30854326	K562	blood:	n/a	chr6:30854029-30854036 chr6:30854029-30854038 chr6:30854027-30854038 chr6:30854028-30854038 chr6:30854029-30854037 chr6:30854027-30854039 chr6:30854028-30854037
20	KAP1	chr6:30852738-30853979	HEK293	kidney:	n/a	n/a
21	POLR2A	chr6:30850520-30854067	MCF-7	breast:	n/a	n/a
22	POLR2A	chr6:30852508-30854482	Hela-S3	cervix:	n/a	n/a
23	ZKSCAN1	chr6:30853692-30854303	Hela-S3	cervix:	n/a	n/a
24	RAD21	chr6:30853539-30854171	Hela-S3	cervix:	n/a	n/a
25	MYC	chr6:30853299-30854188	MCF10A-Er-Src	breast:	n/a	chr6:30854028-30854037 chr6:30854029-30854038 chr6:30853729-30853739 chr6:30853369-30853379
26	MXI1	chr6:30851462-30854889	IMR90	lung:	n/a	chr6:30854399-30854414 chr6:30852833-30852842
27	TAF1	chr6:30853782-30854313	H1-hESC	embryonic stem cell:	n/a	n/a
28	TCF12	chr6:30853237-30854463	A549	lung:	n/a	chr6:30854306-30854316
29	JUND	chr6:30853776-30854293	A549	lung:	n/a	chr6:30854029-30854036 chr6:30854029-30854038 chr6:30854027-30854038 chr6:30854028-30854038 chr6:30854029-30854037 chr6:30854027-30854039 chr6:30854028-30854037
30	TBP	chr6:30853751-30854170	Hela-S3	cervix:	n/a	n/a
31	FOXA2	chr6:30853732-30854176	HepG2	liver:	n/a	n/a
32	JUND	chr6:30853779-30854220	HepG2	liver:	n/a	chr6:30854029-30854036 chr6:30854029-30854038 chr6:30854027-30854038 chr6:30854028-30854038 chr6:30854029-30854037 chr6:30854027-30854039 chr6:30854028-30854037
33	ELK1	chr6:30853713-30854180	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr6:30853593-30854374	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:30853754-30854492	K562	blood:	n/a	n/a
36	SP1	chr6:30853796-30854562	H1-hESC	embryonic stem cell:	n/a	n/a
37	FOSL2	chr6:30853717-30854374	MCF-7	breast:	n/a	chr6:30854029-30854036 chr6:30854029-30854038 chr6:30854028-30854038 chr6:30854026-30854037 chr6:30854029-30854037 chr6:30854027-30854039 chr6:30854028-30854037
38	MAX	chr6:30853073-30854238	MCF-7	breast:	n/a	chr6:30854028-30854037 chr6:30854029-30854038 chr6:30853729-30853739 chr6:30853369-30853379
39	POLR2A	chr6:30853688-30854425	H1-hESC	embryonic stem cell:	n/a	n/a
40	UBTF	chr6:30853448-30854316	K562	blood:	n/a	n/a
41	HDAC2	chr6:30853311-30854236	HepG2	liver:	n/a	chr6:30853491-30853500
42	MAX	chr6:30852442-30854200	MCF-7	breast:	n/a	chr6:30854028-30854037 chr6:30854029-30854038 chr6:30853729-30853739 chr6:30853369-30853379
43	FOXA2	chr6:30853312-30854182	A549	lung:	n/a	n/a
44	FOSL2	chr6:30853611-30854474	A549	lung:	n/a	chr6:30854029-30854036 chr6:30854029-30854038 chr6:30854028-30854038 chr6:30854026-30854037 chr6:30854029-30854037 chr6:30854027-30854039 chr6:30854028-30854037
45	MAX	chr6:30852509-30854600	A549	lung:	n/a	chr6:30854028-30854037 chr6:30854029-30854038 chr6:30854405-30854414 chr6:30853729-30853739 chr6:30853369-30853379
46	TAF7	chr6:30853744-30854387	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr6:30853020-30854547	A549	lung:	n/a	n/a
48	ZNF143	chr6:30853780-30854495	Hela-S3	cervix:	n/a	chr6:30854294-30854309 chr6:30854159-30854169
49	POLR2A	chr6:30853615-30854489	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr6:30853776-30854063	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:30850840..30855328-chr6:30877838..30882665,10	MCF-7	breast:
2	chr6:30456342..30459390-chr6:30850533..30854331,4	MCF-7	breast:
3	chr6:30847750..30854588-chr6:30880214..30885422,8	K562	blood:
4	chr6:30798389..30801828-chr6:30850243..30854490,5	MCF-7	breast:
5	chr6:30717879..30721732-chr6:30850020..30854415,6	MCF-7	breast:
6	chr6:30850549..30855941-chr6:30880357..30883667,13	MCF-7	breast:
7	chr6:30687338..30691474-chr6:30850428..30854318,11	MCF-7	breast:
8	chr6:30849184..30852666-chr6:30852715..30854490,5	K562	blood:
9	chr6:30710692..30712313-chr6:30853038..30855427,2	K562	blood:
10	chr6:30582976..30585649-chr6:30850283..30854979,5	MCF-7	breast:
11	chr6:30705171..30717521-chr6:30843972..30856100,74	MCF-7	breast:
12	chr6:30689083..30692064-chr6:30851539..30853940,2	K562	blood:
13	chr6:30704403..30722478-chr6:30842859..30858629,100	MCF-7	breast:
14	chr6:30848838..30854096-chr6:30874501..30878794,8	MCF-7	breast:
15	chr6:30581806..30587588-chr6:30850201..30854112,13	MCF-7	breast:
16	chr6:30455629..30458030-chr6:30852314..30855015,2	K562	blood:
17	chr6:30830444..30833119-chr6:30851282..30854552,3	MCF-7	breast:
18	chr6:30780598..30803497-chr6:30842531..30855110,80	MCF-7	breast:
19	chr6:30685105..30690458-chr6:30847596..30854595,13	MCF-7	breast:

Variant related genes	Relation type
MIR4640	TF binding region
DDR1	TF binding region
ENSG00000196230	Chromatin interaction
ENSG00000204580	Chromatin interaction
ENSG00000272540	Chromatin interaction
ENSG00000202241	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000204592	Chromatin interaction
ENSG00000214894	Chromatin interaction
ENSG00000137411	Chromatin interaction
ENSG00000213780	Chromatin interaction
ENSG00000264731	Chromatin interaction
ENSG00000222894	Chromatin interaction
ENSG00000263608	Chromatin interaction
ENSG00000137312	Chromatin interaction
ENSG00000272273	Chromatin interaction
ENSG00000137337	Chromatin interaction
ENSG00000137331	Chromatin interaction
ENSG00000204568	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs2253705	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2517459	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2532932	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2894059	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3094108	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3094719	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3095345	0.96[ASN][1000 genomes]
rs3130648	0.93[ASN][1000 genomes]
rs3130779	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3130780	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3130788	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3130797	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3131028	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3131032	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3891155	0.85[AFR][1000 genomes]
rs56366011	0.86[AFR][1000 genomes]
rs58893284	0.83[AFR][1000 genomes]
rs6933400	0.85[AFR][1000 genomes]
rs6933909	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
5	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
6	nsv884109	chr6:30824532-30872203	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv884110	chr6:30845563-30856463	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	nsv884111	chr6:30845563-30864279	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
9	nsv884112	chr6:30845563-30866618	Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
10	nsv601482	chr6:30846830-30854090	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
11	nsv884113	chr6:30846830-30857542	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
12	nsv884114	chr6:30846830-30867830	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
13	nsv884115	chr6:30847710-30858991	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
14	nsv884116	chr6:30848253-30864279	Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
15	nsv884117	chr6:30849124-30862423	Flanking Active TSS Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
16	nsv884118	chr6:30849822-30855907	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
17	nsv884119	chr6:30849822-30856692	Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
18	nsv884120	chr6:30849822-30864279	Genic enhancers Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
19	nsv884121	chr6:30850191-30856692	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
20	nsv884122	chr6:30850191-30858991	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
21	nsv884123	chr6:30850191-30865904	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs3131034	VARS2	cis	lymphoblastoid	seeQTL
rs3131034	PRSS16	cis	cerebellum	SCAN
rs3131034	HIST1H2AL	cis	cerebellum	SCAN

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30850600-30854600	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr6:30850800-30854200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:30850800-30854400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr6:30851400-30854400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:30851800-30854200	Active TSS	Ovary	ovary
6	chr6:30852200-30854000	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr6:30852600-30853800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
8	chr6:30852600-30853800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
9	chr6:30852600-30853800	Flanking Active TSS	Liver	Liver
10	chr6:30852600-30853800	Flanking Active TSS	Placenta	Placenta
11	chr6:30852600-30853800	Flanking Bivalent TSS/Enh	HepG2	liver
12	chr6:30852600-30854000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
13	chr6:30852600-30854000	Flanking Active TSS	Dnd41	blood
14	chr6:30852600-30854200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
15	chr6:30852600-30854200	Flanking Active TSS	Adipose Nuclei	Adipose
16	chr6:30852600-30854400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:30852600-30854400	Flanking Active TSS	Colonic Mucosa	Colon
18	chr6:30852600-30854400	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr6:30852600-30854400	Flanking Active TSS	Fetal Intestine Large	intestine
20	chr6:30852600-30854400	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
21	chr6:30852600-30854400	Flanking Active TSS	Pancreas	Pancrea
22	chr6:30852600-30854600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
23	chr6:30852600-30854600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr6:30852600-30854600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
25	chr6:30852600-30854600	Flanking Active TSS	Osteobl	bone
26	chr6:30852600-30854800	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:30852600-30854800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:30852600-30854800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr6:30852600-30854800	Flanking Active TSS	K562	blood
30	chr6:30852600-30854800	Transcr. at gene 5' and 3'	NHEK	skin
31	chr6:30852600-30855000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr6:30852800-30853800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr6:30852800-30853800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr6:30852800-30853800	Flanking Active TSS	HSMMtube	muscle
35	chr6:30852800-30854000	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:30852800-30854000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr6:30852800-30854000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr6:30852800-30854000	Flanking Active TSS	Fetal Heart	heart
39	chr6:30852800-30854000	Flanking Active TSS	Placenta Amnion	Placenta Amnion
40	chr6:30852800-30854000	Flanking Active TSS	NHDF-Ad	bronchial
41	chr6:30852800-30854200	Flanking Active TSS	Thymus	Thymus
42	chr6:30852800-30854400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:30852800-30854400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
44	chr6:30852800-30854400	Flanking Active TSS	Gastric	stomach
45	chr6:30852800-30854600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:30852800-30854600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:30852800-30854600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr6:30852800-30854600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
49	chr6:30852800-30854600	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
50	chr6:30852800-30854600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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