Variant report

Variant	rs3130461
Chromosome Location	chr6:31164700-31164701
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	CTCF	chr6:31164679-31165141	MCF-7	breast:	n/a	chr6:31164911-31164927
2	POLR2A	chr6:31164617-31166158	GM12878	blood:	n/a	n/a
3	REST	chr6:31164571-31166253	H1-neurons	neurons:	n/a	chr6:31165699-31165712 chr6:31165878-31165885
4	USF1	chr6:31164618-31165012	SK-N-SH_RA	brain:	n/a	chr6:31164872-31164883
5	HEY1	chr6:31164598-31165164	K562	blood:	n/a	n/a
6	POU2F2	chr6:31164689-31165222	GM12891	blood:	n/a	n/a
7	POLR2A	chr6:31164673-31165190	HL-60	blood:	n/a	n/a
8	CBX3	chr6:31164689-31165043	K562	blood:	n/a	n/a
9	RAD21	chr6:31164605-31165675	SK-N-SH	brain:	n/a	chr6:31165440-31165454
10	HCFC1	chr6:31164487-31165093	Hela-S3	cervix:	n/a	n/a
11	YY1	chr6:31164674-31165101	GM12878	blood:	n/a	n/a
12	FOXM1	chr6:31164585-31165150	GM12878	blood:	n/a	n/a
13	POLR2A	chr6:31163839-31166273	SK-N-MC	brain:	n/a	n/a
14	MBD4	chr6:31164662-31165091	HepG2	liver:	n/a	n/a
15	POLR2A	chr6:31164585-31166226	GM12878	blood:	n/a	n/a
16	HEY1	chr6:31164693-31166174	HepG2	liver:	n/a	n/a
17	NFIC	chr6:31164631-31165109	GM12878	blood:	n/a	n/a
18	POLR2A	chr6:31164670-31165126	HepG2	liver:	n/a	n/a
19	POLR2A	chr6:31164037-31166160	Raji	blood:	n/a	n/a
20	RAD21	chr6:31164695-31165031	K562	blood:	n/a	n/a
21	MAX	chr6:31164576-31165181	HepG2	liver:	n/a	chr6:31164872-31164883
22	USF1	chr6:31164698-31165026	HepG2	liver:	n/a	chr6:31164872-31164883
23	POLR2A	chr6:31164696-31165153	SK-N-SH	brain:	n/a	n/a
24	POLR2A	chr6:31164045-31167117	HepG2	liver:	n/a	n/a
25	HEY1	chr6:31164053-31165082	HepG2	liver:	n/a	n/a
26	USF1	chr6:31164617-31165097	A549	lung:	n/a	chr6:31164872-31164883
27	POLR2A	chr6:31164652-31166208	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr6:31164364-31165171	K562	blood:	n/a	n/a
29	ATF3	chr6:31164700-31165037	K562	blood:	n/a	n/a
30	ZNF263	chr6:31164672-31165338	HEK293-T-REx	kidney:	n/a	chr6:31164806-31164827
31	CTCF	chr6:31164694-31165058	A549	lung:	n/a	chr6:31164911-31164927
32	TRIM28	chr6:31164612-31165158	K562	blood:	n/a	n/a
33	STAT5A	chr6:31164610-31165114	GM12878	blood:	n/a	n/a
34	ATF2	chr6:31164674-31165096	H1-hESC	embryonic stem cell:	n/a	n/a
35	SP1	chr6:31164693-31165114	GM12878	blood:	n/a	n/a
36	RAD21	chr6:31164628-31165148	ECC-1	luminal epithelium:	n/a	n/a
37	CTCF	chr6:31164670-31165022	H1-hESC	embryonic stem cell:	n/a	chr6:31164911-31164927
38	USF1	chr6:31164685-31165101	A549	lung:	n/a	chr6:31164872-31164883
39	MEF2A	chr6:31164685-31165120	GM12878	blood:	n/a	n/a
40	MAX	chr6:31164700-31165088	NB4	blood:	n/a	chr6:31164872-31164883
41	E2F6	chr6:31164663-31165052	K562	blood:	n/a	n/a
42	USF1	chr6:31164659-31164980	A549	lung:	n/a	chr6:31164872-31164883
43	POLR2A	chr6:31164564-31165094	K562	blood:	n/a	n/a
44	POLR2A	chr6:31164553-31166293	PFSK-1	brain:	n/a	n/a
45	POLR2A	chr6:31164040-31166132	HepG2	liver:	n/a	n/a
46	POLR2A	chr6:31164527-31165171	HL-60	blood:	n/a	n/a
47	USF2	chr6:31164686-31165065	GM12878	blood:	n/a	chr6:31164872-31164883
48	USF2	chr6:31164627-31165086	Hela-S3	cervix:	n/a	chr6:31164872-31164883
49	PAX5	chr6:31164668-31165181	GM12878	blood:	n/a	n/a
50	RUNX3	chr6:31164607-31165138	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31136027..31137664-chr6:31162988..31165326,2	MCF-7	breast:
2	chr6:31164421..31165403-chr6:31334396..31335415,9	MCF-7	breast:
3	chr6:31163696..31166940-chr6:31333321..31336541,7	MCF-7	breast:
4	chr6:31164428..31165295-chr6:31333347..31334316,2	MCF-7	breast:

Variant related genes	Relation type
HCG27	TF binding region
ENSG00000228432	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs3094606	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3094607	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3094608	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3094609	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3094610	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3095237	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3095238	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3095246	0.93[EUR][1000 genomes]
rs3095252	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3130428	0.93[EUR][1000 genomes]
rs3130460	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3130462	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3130463	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3130466	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3130468	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3130512	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3130518	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3130520	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3130528	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3130532	0.95[EUR][1000 genomes]
rs3130941	0.93[EUR][1000 genomes]
rs3130950	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3130952	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3131017	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3132499	0.95[EUR][1000 genomes]
rs3132500	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3132501	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3132503	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3132504	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3132507	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3132508	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3132509	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3132511	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3132517	0.95[ASN][1000 genomes]
rs3132538	0.87[ASN][1000 genomes]
rs3132540	0.87[ASN][1000 genomes]
rs3134782	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3134789	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4343960	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9264416	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 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	nsv1029442	chr6:31006647-31449207	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
7	nsv427750	chr6:31028290-31234581	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv428140	chr6:31028290-31462106	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	89 gene(s)	inside rSNPs	diseases
9	esv2758042	chr6:31028290-31497106	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
10	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
11	nsv1019637	chr6:31104401-31354706	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
12	nsv1029569	chr6:31104401-31412740	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
13	nsv538174	chr6:31104401-31412740	Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
14	nsv1034391	chr6:31131121-31279595	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
15	nsv1025909	chr6:31131121-31354706	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
16	nsv538175	chr6:31131121-31354706	Active TSS Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
17	nsv1015890	chr6:31131121-31449207	Enhancers Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
18	nsv538176	chr6:31131121-31449207	Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
19	esv32635	chr6:31141504-31250618	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
20	nsv1024887	chr6:31162849-31354706	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
21	nsv538177	chr6:31162849-31354706	Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
22	nsv1015903	chr6:31162849-31412740	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
23	nsv538178	chr6:31162849-31412740	Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
24	nsv1031682	chr6:31162849-31449207	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
25	nsv538179	chr6:31162849-31449207	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS 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	61 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3130461	CCHCR1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31141800-31164800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:31154400-31164800	Weak transcription	Gastric	stomach
3	chr6:31155400-31164800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:31157400-31164800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr6:31160800-31164800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:31163800-31164800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr6:31163800-31165000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:31163800-31165600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:31164000-31164800	Enhancers	Fetal Muscle Leg	muscle
10	chr6:31164200-31164800	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr6:31164200-31164800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
12	chr6:31164200-31164800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
13	chr6:31164200-31164800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
14	chr6:31164200-31164800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
15	chr6:31164200-31164800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
16	chr6:31164200-31164800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
17	chr6:31164200-31164800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr6:31164200-31164800	Transcr. at gene 5' and 3'	K562	blood
19	chr6:31164200-31165000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr6:31164200-31165000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
21	chr6:31164200-31165000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
22	chr6:31164200-31165000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr6:31164200-31165000	Enhancers	Stomach Mucosa	stomach
24	chr6:31164200-31165000	Enhancers	Spleen	Spleen
25	chr6:31164200-31165000	Flanking Active TSS	Dnd41	blood
26	chr6:31164200-31167200	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr6:31164400-31164800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:31164400-31164800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:31164400-31164800	Flanking Active TSS	Primary T cells from cord blood	blood
30	chr6:31164400-31164800	Flanking Active TSS	Primary hematopoietic stem cells	blood
31	chr6:31164400-31164800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
32	chr6:31164400-31164800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr6:31164400-31164800	Enhancers	Fetal Lung	lung
34	chr6:31164400-31164800	Enhancers	Fetal Muscle Trunk	muscle
35	chr6:31164400-31164800	Enhancers	Placenta	Placenta
36	chr6:31164400-31164800	Flanking Active TSS	GM12878-XiMat	blood
37	chr6:31164400-31164800	Flanking Active TSS	Hela-S3	cervix
38	chr6:31164400-31165000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:31164400-31165000	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr6:31164400-31165000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
41	chr6:31164400-31165000	Flanking Active TSS	Duodenum Mucosa	Duodenum
42	chr6:31164400-31165000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr6:31164400-31165000	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr6:31164400-31166600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:31164400-31166800	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr6:31164400-31166800	Active TSS	Colon Smooth Muscle	Colon
47	chr6:31164400-31166800	Active TSS	A549	lung
48	chr6:31164400-31168400	Active TSS	Duodenum Smooth Muscle	Duodenum
49	chr6:31164600-31164800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr6:31164600-31164800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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