Variant report

Variant	rs7895921
Chromosome Location	chr10:5665458-5665459
allele	C/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	chr10:5665138-5665459	GM12878	blood:	n/a	chr10:5665281-5665299
2	CTCF	chr10:5665109-5665482	GM19238	blood:	n/a	chr10:5665281-5665299
3	JUN	chr10:5664906-5665714	K562	blood:	n/a	n/a
4	FOXM1	chr10:5665168-5665464	GM12878	blood:	n/a	n/a
5	NR2F2	chr10:5664893-5665672	MCF-7	breast:	n/a	n/a
6	CTCF	chr10:5665173-5665458	GM10248	blood:	n/a	chr10:5665281-5665299
7	MYC	chr10:5665122-5665471	K562	blood:	n/a	n/a
8	RAD21	chr10:5664796-5665672	HCT-116	colon:	n/a	chr10:5665279-5665298
9	CTCF	chr10:5665012-5665498	H1-hESC	embryonic stem cell:	n/a	chr10:5665281-5665299
10	RAD21	chr10:5664936-5665570	A549	lung:	n/a	chr10:5665279-5665298
11	TCF12	chr10:5664831-5665670	A549	lung:	n/a	n/a
12	TCF12	chr10:5664978-5665622	ECC-1	luminal epithelium:	n/a	n/a
13	TBL1XR1	chr10:5665118-5665466	GM12878	blood:	n/a	n/a
14	RAD21	chr10:5664781-5665664	HCT-116	colon:	n/a	chr10:5665279-5665298
15	ZNF143	chr10:5665050-5665467	H1-hESC	embryonic stem cell:	n/a	n/a
16	RAD21	chr10:5664895-5665604	ECC-1	luminal epithelium:	n/a	chr10:5665279-5665298
17	RAD21	chr10:5664937-5665602	MCF-7	breast:	n/a	chr10:5665279-5665298
18	CTCF	chr10:5664772-5666096	A549	lung:	n/a	chr10:5665281-5665299
19	MAX	chr10:5664885-5665547	A549	lung:	n/a	n/a
20	TBP	chr10:5665300-5665479	K562	blood:	n/a	n/a
21	ZNF263	chr10:5665020-5665525	HEK293-T-REx	kidney:	n/a	chr10:5665232-5665241
22	KAP1	chr10:5665065-5665544	HEK293	kidney:	n/a	n/a
23	RAD21	chr10:5665028-5665496	H1-hESC	embryonic stem cell:	n/a	chr10:5665279-5665298
24	YY1	chr10:5665027-5665500	H1-hESC	embryonic stem cell:	n/a	n/a
25	HDAC2	chr10:5664988-5665600	MCF-7	breast:	n/a	n/a
26	MAX	chr10:5664883-5665600	MCF-7	breast:	n/a	n/a
27	RCOR1	chr10:5665041-5665460	K562	blood:	n/a	n/a
28	CTCF	chr10:5665400-5665550	A549	lung:	n/a	n/a
29	MYBL2	chr10:5664999-5665531	HepG2	liver:	n/a	n/a
30	MAX	chr10:5664851-5665558	MCF-7	breast:	n/a	n/a
31	FOXM1	chr10:5665086-5665655	GM12878	blood:	n/a	n/a
32	POU2F2	chr10:5665114-5665514	GM12891	blood:	n/a	n/a
33	TCF12	chr10:5665072-5665503	H1-hESC	embryonic stem cell:	n/a	n/a
34	RAD21	chr10:5664846-5665673	A549	lung:	n/a	chr10:5665279-5665298
35	SIN3A	chr10:5665105-5665489	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr10:5665144-5665467	Gliobla	brain:	n/a	chr10:5665281-5665299
37	CTCF	chr10:5665078-5665511	K562	blood:	n/a	chr10:5665281-5665299
38	YY1	chr10:5665147-5665459	GM12878	blood:	n/a	n/a
39	PBX3	chr10:5665254-5665458	GM12878	blood:	n/a	n/a
40	ATF3	chr10:5665020-5665576	A549	lung:	n/a	n/a
41	RAD21	chr10:5665020-5665503	H1-hESC	embryonic stem cell:	n/a	chr10:5665279-5665298
42	RAD21	chr10:5664940-5665531	HepG2	liver:	n/a	chr10:5665279-5665298
43	RAD21	chr10:5665077-5665485	A549	lung:	n/a	chr10:5665279-5665298
44	CTCF	chr10:5664939-5665624	HCT-116	colon:	n/a	chr10:5665281-5665299
45	TEAD4	chr10:5665056-5665512	K562	blood:	n/a	n/a
46	NR2F2	chr10:5664978-5665646	MCF-7	breast:	n/a	n/a
47	RAD21	chr10:5664776-5665545	MCF-7	breast:	n/a	chr10:5665279-5665298
48	CTCF	chr10:5665119-5665466	GM19240	blood:	n/a	chr10:5665281-5665299
49	RAD21	chr10:5664920-5665599	H1-hESC	embryonic stem cell:	n/a	chr10:5665279-5665298
50	GATA3	chr10:5664542-5665591	MCF-7	breast:	n/a	chr10:5665198-5665205 chr10:5664740-5664748

No.	Distal block	Cell Line	Cell type
1	chr10:5533027..5543195-chr10:5659124..5672516,23	MCF-7	breast:
2	chr10:5664947..5667027-chr10:5854331..5857046,2	MCF-7	breast:
3	chr10:5595998..5596581-chr10:5664936..5665458,2	MCF-7	breast:
4	chr10:5519924..5522534-chr10:5663921..5666651,2	K562	blood:
5	chr10:5483412..5484324-chr10:5664681..5665600,3	MCF-7	breast:
6	chr10:5483777..5485122-chr10:5664835..5665857,8	MCF-7	breast:
7	chr10:5484376..5493176-chr10:5653017..5671828,35	MCF-7	breast:
8	chr10:5491006..5493868-chr10:5664560..5666317,3	K562	blood:
9	chr10:5487091..5489925-chr10:5665112..5666919,2	K562	blood:
10	chr10:5623488..5628108-chr10:5662504..5666628,7	MCF-7	breast:
11	chr10:4891967..4892493-chr10:5664887..5665773,3	K562	blood:
12	chr10:5665389..5668245-chr10:5681455..5685230,3	MCF-7	breast:
13	chr10:5655010..5657602-chr10:5662784..5666424,4	MCF-7	breast:
14	chr10:5575744..5578406-chr10:5664031..5665635,2	MCF-7	breast:
15	chr10:5664649..5667001-chr10:5672952..5674907,2	K562	blood:
16	chr10:5453685..5455931-chr10:5663712..5666471,2	MCF-7	breast:
17	chr10:5534628..5543320-chr10:5658612..5667994,15	MCF-7	breast:
18	chr10:5478122..5480444-chr10:5662741..5665570,2	MCF-7	breast:
19	chr10:5483715..5496703-chr10:5653374..5669304,43	MCF-7	breast:
20	chr10:5593411..5593958-chr10:5664829..5665548,2	MCF-7	breast:
21	chr10:5664937..5665458-chr10:5701845..5702533,2	MCF-7	breast:
22	chr10:5483755..5485248-chr10:5664796..5665809,8	K562	blood:

Variant related genes	Relation type
ENSG00000228685	TF binding region
ENSG00000173848	Chromatin interaction
ENSG00000240577	Chromatin interaction
ENSG00000178372	Chromatin interaction
ENSG00000196372	Chromatin interaction
ENSG00000057608	Chromatin interaction
ENSG00000272764	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11255593	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11256322	0.88[CEU][hapmap];0.89[CHB][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11256474	0.89[CHB][hapmap]
rs1317212	0.94[CHB][hapmap];0.86[JPT][hapmap]
rs17141741	1.00[GIH][hapmap];0.90[TSI][hapmap];0.92[YRI][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2386655	0.89[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs2386659	0.89[CHB][hapmap];0.86[JPT][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2386660	0.89[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs6602289	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7896306	0.86[MEX][hapmap]
rs7912120	0.86[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv894798	chr10:5503610-5670275	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv523491	chr10:5542109-5720067	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	esv2757364	chr10:5557024-5720512	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	esv2759729	chr10:5557024-5804780	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
6	esv2758209	chr10:5637111-5804780	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv1040932	chr10:5637870-5665774	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv894806	chr10:5643511-5670275	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1054888	chr10:5645033-5694612	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv519582	chr10:5646103-5720067	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	nsv894807	chr10:5647942-5691135	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
12	nsv8599	chr10:5649129-5719928	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	nsv1050965	chr10:5649760-5717125	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
14	nsv1044330	chr10:5652006-5717125	Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription 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	22 gene(s)	inside rSNPs	diseases
15	nsv975791	chr10:5652225-5711077	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
16	nsv466720	chr10:5652277-5715401	Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
17	nsv549892	chr10:5652277-5715401	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
18	nsv1037709	chr10:5652739-5717125	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
19	nsv470917	chr10:5654167-5715401	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
20	nsv818742	chr10:5654167-5715401	Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
21	nsv1036492	chr10:5656962-5711147	Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
22	nsv540473	chr10:5656962-5711147	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
23	nsv1036253	chr10:5657162-5711008	Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
24	nsv540474	chr10:5657162-5711008	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic 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	22 gene(s)	inside rSNPs	diseases
25	nsv1040422	chr10:5665458-5714630	Active TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
26	nsv1043251	chr10:5665458-5716555	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
27	nsv1052519	chr10:5665458-5717125	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS Genic enhancers 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	20 gene(s)	inside rSNPs	diseases
28	nsv1038690	chr10:5665458-5720424	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
29	nsv1039650	chr10:5665458-5720512	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
30	nsv1041684	chr10:5665458-5722299	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription 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	21 gene(s)	inside rSNPs	diseases
31	esv2760149	chr10:5665458-5724382	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
32	nsv1054909	chr10:5665458-5724382	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
33	nsv1049620	chr10:5665458-5725208	Bivalent/Poised TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active 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	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5658000-5673600	Weak transcription	Left Ventricle	heart
2	chr10:5661600-5667800	Weak transcription	HSMMtube	muscle
3	chr10:5661600-5670000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr10:5661600-5670200	Weak transcription	Right Atrium	heart
5	chr10:5662200-5669800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:5662200-5670600	Weak transcription	Fetal Lung	lung
7	chr10:5662600-5668400	Weak transcription	NH-A	brain
8	chr10:5662800-5666600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:5662800-5667800	Weak transcription	Ovary	ovary
10	chr10:5663400-5669800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:5663800-5665800	Enhancers	Adipose Nuclei	Adipose
12	chr10:5664000-5665600	Enhancers	NHEK	skin
13	chr10:5664000-5665800	Enhancers	Fetal Muscle Leg	muscle
14	chr10:5664000-5670200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr10:5664400-5665800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr10:5664600-5665600	Enhancers	A549	lung
17	chr10:5664600-5665600	Enhancers	HMEC	breast
18	chr10:5664800-5665600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:5664800-5665600	Enhancers	Fetal Intestine Small	intestine
20	chr10:5664800-5666000	Enhancers	Fetal Muscle Trunk	muscle
21	chr10:5665000-5665600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr10:5665000-5665600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr10:5665000-5665600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr10:5665000-5665600	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr10:5665000-5665600	Enhancers	Primary B cells from peripheral blood	blood
26	chr10:5665000-5665600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr10:5665000-5665600	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr10:5665000-5665600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr10:5665000-5665600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr10:5665000-5665600	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr10:5665000-5665600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr10:5665000-5665600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr10:5665000-5665600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr10:5665000-5665600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr10:5665000-5665600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:5665000-5665600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr10:5665000-5665600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr10:5665000-5665600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr10:5665000-5665600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr10:5665000-5665600	Enhancers	Aorta	Aorta
41	chr10:5665000-5665600	Enhancers	Brain Cingulate Gyrus	brain
42	chr10:5665000-5665600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr10:5665000-5665600	Enhancers	Brain Substantia Nigra	brain
44	chr10:5665000-5665600	Enhancers	Colonic Mucosa	Colon
45	chr10:5665000-5665600	Enhancers	Colon Smooth Muscle	Colon
46	chr10:5665000-5665600	Enhancers	Duodenum Mucosa	Duodenum
47	chr10:5665000-5665600	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr10:5665000-5665600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr10:5665000-5665600	Enhancers	Placenta	Placenta
50	chr10:5665000-5665600	Enhancers	Gastric	stomach

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