Variant report

Variant	rs28397269
Chromosome Location	chr6:31164595-31164596
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	REST	chr6:31164571-31166253	H1-neurons	neurons:	n/a	chr6:31165699-31165712 chr6:31165878-31165885
2	HCFC1	chr6:31164487-31165093	Hela-S3	cervix:	n/a	n/a
3	FOXM1	chr6:31164585-31165150	GM12878	blood:	n/a	n/a
4	POLR2A	chr6:31163839-31166273	SK-N-MC	brain:	n/a	n/a
5	POLR2A	chr6:31164585-31166226	GM12878	blood:	n/a	n/a
6	POLR2A	chr6:31164037-31166160	Raji	blood:	n/a	n/a
7	MAX	chr6:31164576-31165181	HepG2	liver:	n/a	chr6:31164872-31164883
8	POLR2A	chr6:31164045-31167117	HepG2	liver:	n/a	n/a
9	HEY1	chr6:31164053-31165082	HepG2	liver:	n/a	n/a
10	CBX3	chr6:31164364-31165171	K562	blood:	n/a	n/a
11	POLR2A	chr6:31164564-31165094	K562	blood:	n/a	n/a
12	POLR2A	chr6:31164553-31166293	PFSK-1	brain:	n/a	n/a
13	POLR2A	chr6:31164040-31166132	HepG2	liver:	n/a	n/a
14	POLR2A	chr6:31164527-31165171	HL-60	blood:	n/a	n/a
15	POLR2A	chr6:31164502-31166212	K562	blood:	n/a	n/a
16	POLR2A	chr6:31164439-31166135	MCF-7	breast:	n/a	n/a
17	HEY1	chr6:31163982-31166189	K562	blood:	n/a	n/a
18	USF1	chr6:31164564-31165201	SK-N-SH	brain:	n/a	chr6:31164872-31164883
19	POLR2A	chr6:31164018-31165904	HCT-116	colon:	n/a	n/a
20	USF1	chr6:31164570-31165190	HCT-116	colon:	n/a	chr6:31164872-31164883
21	USF1	chr6:31164518-31165173	HCT-116	colon:	n/a	chr6:31164872-31164883
22	POLR2A	chr6:31164533-31166226	GM12892	blood:	n/a	n/a
23	CTCF	chr6:31164564-31165140	HCT-116	colon:	n/a	chr6:31164911-31164927
24	RAD21	chr6:31164549-31165675	MCF-7	breast:	n/a	chr6:31165440-31165454
25	PML	chr6:31164576-31166354	GM12878	blood:	n/a	n/a
26	MBD4	chr6:31164523-31165107	HepG2	liver:	n/a	n/a
27	POLR2A	chr6:31164078-31165099	ECC-1	luminal epithelium:	n/a	n/a
28	USF1	chr6:31164594-31165103	H1-hESC	embryonic stem cell:	n/a	chr6:31164872-31164883
29	POLR2A	chr6:31164594-31166086	MCF-7	breast:	n/a	n/a
30	MXI1	chr6:31164537-31165137	SK-N-SH	brain:	n/a	n/a
31	USF1	chr6:31164567-31165153	SK-N-SH	brain:	n/a	chr6:31164872-31164883
32	RAD21	chr6:31164590-31165052	A549	lung:	n/a	n/a
33	MYBL2	chr6:31164539-31166215	HepG2	liver:	n/a	n/a
34	NFIC	chr6:31164578-31165115	HepG2	liver:	n/a	n/a
35	MTA3	chr6:31164524-31166339	GM12878	blood:	n/a	n/a
36	MAX	chr6:31164551-31165094	K562	blood:	n/a	chr6:31164872-31164883
37	TEAD4	chr6:31164586-31165099	K562	blood:	n/a	n/a
38	POLR2A	chr6:31163971-31165175	HepG2	liver:	n/a	n/a
39	CREB1	chr6:31164585-31166176	HepG2	liver:	n/a	n/a
40	CTCF	chr6:31164540-31166211	SK-N-SH	brain:	n/a	chr6:31165441-31165454 chr6:31164911-31164927
41	BCLAF1	chr6:31164582-31165102	GM12878	blood:	n/a	n/a
42	E2F6	chr6:31164511-31165096	H1-hESC	embryonic stem cell:	n/a	n/a
43	RAD21	chr6:31164506-31165156	HCT-116	colon:	n/a	n/a
44	NR2F2	chr6:31164591-31165842	MCF-7	breast:	n/a	n/a
45	POLR2A	chr6:31164032-31166203	PBDE	blood:	n/a	n/a
46	POLR2A	chr6:31164573-31165103	ECC-1	luminal epithelium:	n/a	n/a
47	POLR2A	chr6:31164033-31166331	K562	blood:	n/a	n/a
48	NR2F2	chr6:31164500-31166335	K562	blood:	n/a	n/a
49	CTCF	chr6:31164516-31165695	HCT-116	colon:	n/a	chr6:31165441-31165454 chr6:31164911-31164927
50	CHD1	chr6:31164526-31166307	IMR90	lung:	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: 118 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs1052989	0.80[AFR][1000 genomes]
rs1135811	0.83[ASN][1000 genomes]
rs11381232	0.81[AFR][1000 genomes]
rs11507945	0.81[AFR][1000 genomes]
rs11961945	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11961983	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11967629	0.83[AFR][1000 genomes]
rs17191181	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17191237	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17197540	0.83[ASN][1000 genomes]
rs2394892	0.80[EUR][1000 genomes]
rs28360055	0.88[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28360056	0.88[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28360057	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28360058	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28360059	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28360060	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs28360061	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs28360062	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs28360063	0.90[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs28360064	0.81[AFR][1000 genomes]
rs28360065	0.80[AFR][1000 genomes]
rs28360067	0.98[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs28397268	0.86[AFR][1000 genomes]
rs28397270	0.82[AFR][1000 genomes]
rs28397271	0.84[AFR][1000 genomes]
rs28397276	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs28397277	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28397284	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28397285	0.81[AFR][1000 genomes]
rs28397286	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs28397293	0.81[EUR][1000 genomes]
rs28397294	0.80[EUR][1000 genomes]
rs28397295	0.80[EUR][1000 genomes]
rs28397296	0.80[EUR][1000 genomes]
rs28397297	0.80[EUR][1000 genomes]
rs28397300	0.80[EUR][1000 genomes]
rs28749548	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28749549	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28749550	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28749551	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3887153	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4122189	0.81[AFR][1000 genomes]
rs4713441	0.88[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs4713442	0.91[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs6457349	0.85[EUR][1000 genomes]
rs6457350	0.85[EUR][1000 genomes]
rs6899874	0.81[AFR][1000 genomes]
rs6899875	0.88[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs6901685	0.82[AFR][1000 genomes]
rs6907451	0.85[ASN][1000 genomes]
rs6908994	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6913015	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6913470	0.81[ASN][1000 genomes]
rs6913648	0.80[ASN][1000 genomes]
rs6913863	0.83[ASN][1000 genomes]
rs6914030	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6914393	0.87[ASN][1000 genomes]
rs6914706	0.89[ASN][1000 genomes]
rs6914710	0.89[ASN][1000 genomes]
rs6919493	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6922077	0.82[AFR][1000 genomes]
rs6922553	0.82[AFR][1000 genomes]
rs6922756	0.80[AFR][1000 genomes]
rs6922842	0.81[AFR][1000 genomes]
rs6922994	0.82[AFR][1000 genomes]
rs6927253	0.84[AFR][1000 genomes]
rs6927324	0.81[ASN][1000 genomes]
rs6930438	0.83[ASN][1000 genomes]
rs6932070	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6936474	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs6936597	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs6941912	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7453202	0.83[ASN][1000 genomes]
rs7745050	0.82[EUR][1000 genomes]
rs7745197	0.81[EUR][1000 genomes]
rs7745906	0.85[EUR][1000 genomes]
rs7755702	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7768431	0.85[EUR][1000 genomes]
rs915660	0.83[AFR][1000 genomes]
rs9295957	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9295958	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9357109	0.83[AFR][1000 genomes]
rs9357113	0.85[AFR][1000 genomes]
rs9357115	0.90[AFR][1000 genomes]
rs9378115	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9380220	0.83[AFR][1000 genomes]
rs9380221	0.84[AFR][1000 genomes]
rs9380223	0.82[AFR][1000 genomes]
rs9391712	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9391818	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9394042	0.81[AFR][1000 genomes]
rs9405052	0.88[AFR][1000 genomes];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:5)

SNP	Gene	Cis/trans	Tissue	Source
rs28397269	CCHCR1	Cis_1M	lymphoblastoid	RTeQTL
rs28397269	TCF19	Cis_1M	lymphoblastoid	RTeQTL
rs28397269	HLA-B	Cis_1M	lymphoblastoid	RTeQTL
rs28397269	DDR1	Cis_1M	lymphoblastoid	RTeQTL
rs28397269	HLA-C	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31141800-31164800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:31154200-31164600	Weak transcription	Left Ventricle	heart
3	chr6:31154200-31164600	Weak transcription	Right Atrium	heart
4	chr6:31154400-31164600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr6:31154400-31164800	Weak transcription	Gastric	stomach
6	chr6:31155400-31164800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:31157400-31164600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:31157400-31164800	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr6:31160600-31164600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:31160800-31164800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:31161200-31164600	Weak transcription	Brain Anterior Caudate	brain
12	chr6:31161800-31164600	Weak transcription	Thymus	Thymus
13	chr6:31162200-31164600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:31162800-31164600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:31162800-31164600	Weak transcription	Brain Angular Gyrus	brain
16	chr6:31163800-31164600	Enhancers	Primary B cells from peripheral blood	blood
17	chr6:31163800-31164600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:31163800-31164800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
19	chr6:31163800-31165000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:31163800-31165600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:31164000-31164600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:31164000-31164800	Enhancers	Fetal Muscle Leg	muscle
23	chr6:31164200-31164600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr6:31164200-31164600	Enhancers	Adipose Nuclei	Adipose
25	chr6:31164200-31164600	Enhancers	Liver	Liver
26	chr6:31164200-31164600	Enhancers	Brain Germinal Matrix	brain
27	chr6:31164200-31164600	Enhancers	Brain Substantia Nigra	brain
28	chr6:31164200-31164600	Enhancers	Fetal Intestine Large	intestine
29	chr6:31164200-31164600	Enhancers	Lung	lung
30	chr6:31164200-31164600	Enhancers	Psoas Muscle	Psoas
31	chr6:31164200-31164600	Enhancers	HepG2	liver
32	chr6:31164200-31164800	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr6:31164200-31164800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
34	chr6:31164200-31164800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr6:31164200-31164800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr6:31164200-31164800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr6:31164200-31164800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr6:31164200-31164800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr6:31164200-31164800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:31164200-31164800	Transcr. at gene 5' and 3'	K562	blood
41	chr6:31164200-31165000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
42	chr6:31164200-31165000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr6:31164200-31165000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
44	chr6:31164200-31165000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr6:31164200-31165000	Enhancers	Stomach Mucosa	stomach
46	chr6:31164200-31165000	Enhancers	Spleen	Spleen
47	chr6:31164200-31165000	Flanking Active TSS	Dnd41	blood
48	chr6:31164200-31167200	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr6:31164400-31164600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr6:31164400-31164600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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