Variant report

Variant	rs4930192
Chromosome Location	chr11:67070017-67070018
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	USF1	chr11:67069849-67070452	ECC-1	luminal epithelium:	n/a	chr11:67070154-67070175
2	MXI1	chr11:67069958-67070587	H1-hESC	embryonic stem cell:	n/a	n/a
3	TFAP2A	chr11:67069663-67071991	Hela-S3	cervix:	n/a	chr11:67071564-67071575 chr11:67071268-67071276 chr11:67071663-67071671 chr11:67071564-67071575 chr11:67071907-67071919 chr11:67070800-67070815 chr11:67071564-67071575 chr11:67071268-67071276 chr11:67071269-67071277 chr11:67071564-67071575 chr11:67071229-67071240 chr11:67070833-67070845 chr11:67071663-67071671 chr11:67071269-67071277 chr11:67070302-67070314 chr11:67071269-67071277 chr11:67071268-67071276 chr11:67071663-67071671
4	RFX5	chr11:67069705-67070576	Hela-S3	cervix:	n/a	n/a
5	TFAP2C	chr11:67069594-67071982	Hela-S3	cervix:	n/a	chr11:67070859-67070874 chr11:67071563-67071578
6	CTBP2	chr11:67069708-67071107	H1-hESC	embryonic stem cell:	n/a	n/a
7	USF1	chr11:67069880-67070378	H1-hESC	embryonic stem cell:	n/a	chr11:67070154-67070175
8	BCL3	chr11:67069961-67070895	A549	lung:	n/a	chr11:67070002-67070010 chr11:67070419-67070428 chr11:67070828-67070841
9	TCF12	chr11:67069552-67071878	ECC-1	luminal epithelium:	n/a	chr11:67070822-67070829
10	NFYA	chr11:67069659-67070201	Hela-S3	cervix:	n/a	n/a
11	MAZ	chr11:67069497-67072451	IMR90	lung:	n/a	chr11:67070837-67070847 chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67071385-67071395 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67071867-67071883 chr11:67070274-67070281 chr11:67071259-67071269 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
12	POLR2A	chr11:67069431-67072015	MCF-7	breast:	n/a	n/a
13	TCF7L2	chr11:67069782-67070277	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr11:67069503-67071556	PANC-1	pancreas:	n/a	n/a
15	POLR2A	chr11:67069981-67071411	U87	brain:	n/a	n/a
16	GTF2F1	chr11:67069800-67070752	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr11:67069946-67071695	HepG2	liver:	n/a	n/a
18	POLR2A	chr11:67069889-67071231	K562	blood:	n/a	n/a
19	ELK4	chr11:67069837-67070875	Hela-S3	cervix:	n/a	chr11:67070417-67070428
20	POLR2A	chr11:67069836-67071384	GM12892	blood:	n/a	n/a
21	POLR2A	chr11:67069929-67070445	GM12891	blood:	n/a	n/a
22	MXI1	chr11:67069673-67071082	Hela-S3	cervix:	n/a	n/a
23	MAX	chr11:67069515-67070615	ECC-1	luminal epithelium:	n/a	chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67070273-67070283 chr11:67070274-67070281 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
24	RCOR1	chr11:67069656-67070035	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr11:67069913-67070536	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr11:67069978-67070771	GM12891	blood:	n/a	n/a
27	USF2	chr11:67069756-67070611	Hela-S3	cervix:	n/a	chr11:67070154-67070175 chr11:67070158-67070169
28	SMARCC1	chr11:67069862-67071742	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr11:67069866-67070457	ProgFib	skin:	n/a	n/a
30	MAX	chr11:67069649-67071177	Hela-S3	cervix:	n/a	chr11:67070837-67070847 chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67070273-67070283 chr11:67070274-67070281 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
31	HCFC1	chr11:67069197-67071946	Hela-S3	cervix:	n/a	n/a
32	NFIC	chr11:67069587-67070059	ECC-1	luminal epithelium:	n/a	n/a
33	PBX3	chr11:67069555-67071336	A549	lung:	n/a	n/a
34	MAFK	chr11:67069782-67070038	Hela-S3	cervix:	n/a	n/a
35	NR2F2	chr11:67070007-67071947	MCF-7	breast:	n/a	n/a
36	MAX	chr11:67069587-67071781	ECC-1	luminal epithelium:	n/a	chr11:67070837-67070847 chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67071385-67071395 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67070273-67070283 chr11:67070274-67070281 chr11:67071259-67071269 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
37	MAX	chr11:67069993-67072149	A549	lung:	n/a	chr11:67070837-67070847 chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67071385-67071395 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67071867-67071883 chr11:67070273-67070283 chr11:67070274-67070281 chr11:67071259-67071269 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
38	ZKSCAN1	chr11:67069871-67070339	Hela-S3	cervix:	n/a	n/a
39	ZBTB7A	chr11:67069664-67072102	ECC-1	luminal epithelium:	n/a	chr11:67071264-67071272 chr11:67070600-67070608 chr11:67071630-67071639 chr11:67071400-67071411
40	POLR2A	chr11:67069895-67071244	K562	blood:	n/a	n/a
41	SIN3AK20	chr11:67069436-67072792	MCF-7	breast:	n/a	n/a
42	CHD2	chr11:67069651-67071220	Hela-S3	cervix:	n/a	chr11:67070842-67070852
43	ZBTB7A	chr11:67069746-67072178	ECC-1	luminal epithelium:	n/a	chr11:67071264-67071272 chr11:67070600-67070608 chr11:67071630-67071639 chr11:67071400-67071411
44	POLR2A	chr11:67066339-67071400	HL-60	blood:	n/a	n/a
45	USF2	chr11:67069971-67070356	H1-hESC	embryonic stem cell:	n/a	chr11:67070154-67070175 chr11:67070158-67070169
46	TBP	chr11:67069751-67070036	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr11:67069377-67071188	PFSK-1	brain:	n/a	n/a
48	POLR2A	chr11:67069350-67071191	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr11:67069642-67070056	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr11:67069898-67072555	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67069460..67071861-chr11:67118830..67121727,4	MCF-7	breast:
2	chr11:67069246..67073295-chr11:67139634..67145393,8	MCF-7	breast:
3	chr11:67069872..67072644-chr11:67140515..67142125,2	K562	blood:
4	chr11:67069815..67070639-chr12:108955357..108956118,2	Hela-S3	cervix:
5	chr11:67069155..67071597-chr11:67234852..67239277,5	MCF-7	breast:
6	chr11:67054455..67063331-chr11:67064649..67075279,24	K562	blood:
7	chr11:67069791..67071479-chr19:39339670..39341309,2	MCF-7	breast:
8	chr11:67069948..67073118-chr11:67121673..67124639,3	MCF-7	breast:
9	chr11:67069839..67071996-chr11:67139740..67141397,2	MCF-7	breast:
10	chr11:67069895..67070875-chr22:36023878..36024555,2	HCT-116	colon:

Variant related genes	Relation type
SSH3	TF binding region
ENSG00000175482	Chromatin interaction
ENSG00000175505	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000104824	Chromatin interaction
ENSG00000172932	Chromatin interaction
ENSG00000256514	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10896167	1.00[CEU][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.90[TSI][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10896168	0.86[ASN][1000 genomes]
rs10896169	0.84[ASN][1000 genomes]
rs10896172	0.81[CHB][hapmap]
rs1115051	0.81[ASN][1000 genomes]
rs11227756	0.83[CHD][hapmap];0.90[TSI][hapmap]
rs11601700	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12288048	0.88[MEX][hapmap]
rs12288107	0.83[GIH][hapmap]
rs12290164	0.83[GIH][hapmap];0.86[JPT][hapmap]
rs12788752	0.88[CEU][hapmap];0.83[CHD][hapmap];0.92[JPT][hapmap]
rs12791853	0.83[GIH][hapmap]
rs1540135	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1558256	0.86[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap]
rs1558257	0.81[CHB][hapmap]
rs1638566	1.00[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.90[TSI][hapmap];0.88[EUR][1000 genomes]
rs1638567	1.00[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.90[TSI][hapmap];0.88[EUR][1000 genomes]
rs1638571	1.00[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.90[TSI][hapmap];0.81[EUR][1000 genomes]
rs1638574	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1638586	0.83[GIH][hapmap]
rs1790733	0.83[GIH][hapmap]
rs1790737	0.88[MEX][hapmap]
rs1790738	0.88[MEX][hapmap]
rs1790740	1.00[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.90[TSI][hapmap];0.88[EUR][1000 genomes]
rs1790747	0.83[GIH][hapmap]
rs1944096	0.88[MEX][hapmap]
rs2066496	0.88[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.81[TSI][hapmap];0.87[ASN][1000 genomes]
rs2071007	0.83[CHD][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2256154	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs2286620	0.88[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.86[ASN][1000 genomes]
rs2298815	0.83[GIH][hapmap];0.88[MEX][hapmap]
rs2429462	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2514256	0.88[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap]
rs2514258	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2532605	0.88[MEX][hapmap]
rs3737460	0.83[GIH][hapmap];0.88[MEX][hapmap]
rs3758943	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap]
rs3781941	1.00[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.90[TSI][hapmap];0.88[EUR][1000 genomes]
rs3781942	1.00[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.90[TSI][hapmap];0.88[EUR][1000 genomes]
rs3781943	1.00[CEU][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.81[TSI][hapmap];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3909168	0.88[EUR][1000 genomes]
rs3927807	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs4244819	1.00[CEU][hapmap];0.83[CHD][hapmap];0.85[GIH][hapmap];0.90[TSI][hapmap]
rs4255546	1.00[CEU][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.90[TSI][hapmap];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4375446	1.00[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.90[TSI][hapmap]
rs4478996	1.00[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.81[TSI][hapmap]
rs4503557	0.82[EUR][1000 genomes]
rs4542419	0.83[CHD][hapmap];0.90[TSI][hapmap];0.82[EUR][1000 genomes]
rs4930197	1.00[CEU][hapmap];0.86[CHD][hapmap];0.92[JPT][hapmap];0.90[TSI][hapmap];0.86[EUR][1000 genomes]
rs4930418	0.94[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56337023	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6591239	0.82[EUR][1000 genomes]
rs660960	0.82[EUR][1000 genomes]
rs674499	1.00[GIH][hapmap];0.89[TSI][hapmap];0.91[EUR][1000 genomes]
rs7106352	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7113390	0.82[EUR][1000 genomes]
rs7480390	0.88[CEU][hapmap];0.92[JPT][hapmap]
rs872110	0.88[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers 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	271 gene(s)	inside rSNPs	diseases
2	nsv933183	chr11:67008447-67160993	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv897796	chr11:67021518-67186000	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
4	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
5	nsv897799	chr11:67024534-67072623	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv897800	chr11:67024534-67086298	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
8	nsv468603	chr11:67033076-67164495	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
9	nsv555253	chr11:67033076-67164495	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
10	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
11	nsv897802	chr11:67051245-67075024	Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
12	nsv1047890	chr11:67058231-67184436	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
13	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
14	nsv897803	chr11:67067075-67084761	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers 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	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4930192	RPS6KB2	cis	lymphoblastoid	seeQTL

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67062200-67070400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:67063800-67070400	Strong transcription	Dnd41	blood
3	chr11:67064400-67070400	Strong transcription	Primary B cells from peripheral blood	blood
4	chr11:67065800-67070200	Strong transcription	Thymus	Thymus
5	chr11:67066400-67070200	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr11:67067000-67070200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr11:67067000-67072600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:67067800-67071000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:67068000-67070200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr11:67068400-67070200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:67068400-67070200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:67068800-67070600	Genic enhancers	Spleen	Spleen
13	chr11:67069000-67070200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr11:67069000-67070200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr11:67069000-67070200	Weak transcription	HUVEC	blood vessel
16	chr11:67069000-67070400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr11:67069000-67070600	Flanking Active TSS	Hela-S3	cervix
18	chr11:67069200-67070200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:67069200-67070200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr11:67069200-67070200	Genic enhancers	Muscle Satellite Cultured Cells	--
21	chr11:67069200-67070200	Weak transcription	Aorta	Aorta
22	chr11:67069200-67070200	Genic enhancers	Sigmoid Colon	Sigmoid Colon
23	chr11:67069200-67070600	Enhancers	Fetal Heart	heart
24	chr11:67069200-67070600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
25	chr11:67069200-67073600	Weak transcription	GM12878-XiMat	blood
26	chr11:67069200-67079200	Weak transcription	K562	blood
27	chr11:67069400-67070200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:67069400-67070200	Enhancers	Brain Anterior Caudate	brain
29	chr11:67069400-67070200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr11:67069400-67070200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr11:67069400-67070200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr11:67069400-67070400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr11:67069400-67070400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr11:67069400-67070400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
35	chr11:67069400-67070400	Enhancers	Primary B cells from cord blood	blood
36	chr11:67069400-67070400	Transcr. at gene 5' and 3'	Placenta	Placenta
37	chr11:67069400-67070600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
38	chr11:67069400-67070600	Genic enhancers	NHLF	lung
39	chr11:67069400-67070800	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr11:67069400-67070800	Flanking Active TSS	Liver	Liver
41	chr11:67069400-67071600	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr11:67069400-67072400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:67069600-67070200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:67069600-67070200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:67069600-67070200	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
46	chr11:67069600-67070200	Genic enhancers	NHEK	skin
47	chr11:67069600-67070400	Flanking Active TSS	Fetal Intestine Large	intestine
48	chr11:67069600-67070600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr11:67069600-67070600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:67069600-67070600	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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