Variant report

Variant	rs3809776
Chromosome Location	chr17:46696123-46696124
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:307)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr17:46696020-46696170	GM12873	blood:	n/a	n/a
2	CTCF	chr17:46696060-46696210	K562	blood:	n/a	n/a
3	CTCF	chr17:46695981-46696235	SK-N-SH_RA	brain:	n/a	n/a
4	CTCF	chr17:46696060-46696210	BJ	skin:	n/a	n/a
5	CTCF	chr17:46696000-46696150	HMEC	breast:	n/a	n/a
6	TCF7L2	chr17:46695969-46697602	PANC-1	pancreas:	n/a	chr17:46696732-46696742
7	CTCF	chr17:46695972-46696250	NHEK	skin:	n/a	n/a
8	ELF1	chr17:46695930-46696226	GM12878	blood:	n/a	n/a
9	SMC3	chr17:46695658-46696330	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr17:46695935-46696263	H1-hESC	embryonic stem cell:	n/a	n/a
11	SP1	chr17:46695792-46696329	A549	lung:	n/a	n/a
12	CTCF	chr17:46696040-46696190	HRPEpiC	eye:	n/a	n/a
13	CTCF	chr17:46695976-46696276	LNCaP	prostate:	n/a	n/a
14	CTCF	chr17:46695994-46696252	MCF-7	breast:	n/a	n/a
15	CTCF	chr17:46696080-46696230	GM06990	blood:	n/a	n/a
16	CTCF	chr17:46696060-46696210	GM12878	blood:	n/a	n/a
17	GTF2F1	chr17:46695910-46696239	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr17:46695995-46696251	ProgFib	skin:	n/a	n/a
19	YY1	chr17:46695967-46696271	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr17:46696040-46696190	HA-sp	spinal cord:	n/a	n/a
21	CTBP2	chr17:46696014-46696697	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr17:46696040-46696190	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr17:46696120-46696270	HVMF	connective:	n/a	n/a
24	CTCF	chr17:46696020-46696170	GM12870	blood:	n/a	n/a
25	CTCF	chr17:46695967-46696266	GM19238	blood:	n/a	n/a
26	CTCF	chr17:46696080-46696230	MCF-7	breast:	n/a	n/a
27	SRF	chr17:46696043-46696152	HepG2	liver:	n/a	n/a
28	CHD1	chr17:46695766-46696589	IMR90	lung:	n/a	n/a
29	BHLHE40	chr17:46695972-46696215	K562	blood:	n/a	n/a
30	CTCF	chr17:46696020-46696170	GM12872	blood:	n/a	n/a
31	ELK1	chr17:46696055-46696257	K562	blood:	n/a	n/a
32	RAD21	chr17:46695834-46696367	HepG2	liver:	n/a	n/a
33	TBL1XR1	chr17:46695970-46696828	K562	blood:	n/a	n/a
34	YY1	chr17:46695978-46696191	K562	blood:	n/a	n/a
35	SMC3	chr17:46695867-46696317	K562	blood:	n/a	n/a
36	CTCF	chr17:46695522-46696618	HCT-116	colon:	n/a	n/a
37	CCNT2	chr17:46696017-46696994	K562	blood:	n/a	n/a
38	UBTF	chr17:46696003-46696206	K562	blood:	n/a	n/a
39	BRCA1	chr17:46695959-46696271	Hela-S3	cervix:	n/a	n/a
40	WRNIP1	chr17:46696088-46696224	GM12878	blood:	n/a	n/a
41	FOSL2	chr17:46695838-46696449	A549	lung:	n/a	n/a
42	CTCF	chr17:46695966-46696284	Medullo	brain:	n/a	n/a
43	STAT5A	chr17:46695834-46696303	K562	blood:	n/a	n/a
44	CTCF	chr17:46696040-46696190	K562	blood:	n/a	n/a
45	CTCF	chr17:46695922-46696276	HepG2	liver:	n/a	n/a
46	CTCF	chr17:46696040-46696190	GM12872	blood:	n/a	n/a
47	ZKSCAN1	chr17:46695966-46696205	Hela-S3	cervix:	n/a	n/a
48	RCOR1	chr17:46696014-46696257	HepG2	liver:	n/a	n/a
49	ZBTB7A	chr17:46695982-46696204	K562	blood:	n/a	n/a
50	CTCF	chr17:46695949-46696280	T-47D	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46696077-46696127	AG10803	skin:	n/a
2	chr17:46696077-46696127	NB4	blood:	n/a
3	chr17:46696077-46696127	PFSK-1	brain:	n/a
4	chr17:46696077-46696127	NHDF-neo	bronchial:	n/a
5	chr17:46696077-46696127	RPTEC	kidney:	n/a
6	chr17:46696077-46696127	HRPEpiC	eye:	n/a
7	chr17:46696077-46696127	HNPCEpiC	eye:	n/a
8	chr17:46696077-46696127	A549	lung:	n/a
9	chr17:46696077-46696127	U87	brain:	n/a
10	chr17:46696077-46696127	NHBE	bronchial:	n/a
11	chr17:46696077-46696127	AG09309	skin:	n/a
12	chr17:46696077-46696127	ovcar-3	ovarian:	n/a
13	chr17:46696077-46696127	HEK293	kidney:	embryo
14	chr17:46696077-46696127	HCM	heart:	n/a
15	chr17:46696077-46696127	LNCaP	prostate:	n/a
16	chr17:46696077-46696127	BE2_C	brain:	n/a
17	chr17:46696077-46696127	Hepatocyte	liver:	n/a
18	chr17:46696077-46696127	ProgFib	skin:	n/a
19	chr17:46696077-46696127	IMR90	lung:	fetal
20	chr17:46696077-46696127	HMEC	breast:	n/a
21	chr17:46696077-46696127	T-47D	breast:	n/a
22	chr17:46696077-46696127	AG09319	gingival:	n/a
23	chr17:46696077-46696127	HRE	kidney:	n/a
24	chr17:46696077-46696127	SK-N-MC	brain:	n/a
25	chr17:46696077-46696127	CMK	blood:	n/a
26	chr17:46696077-46696127	HL-60	blood:	n/a
27	chr17:46696077-46696127	NT2-D1	testis:	n/a
28	chr17:46696077-46696127	HRCEpiC	kidney:	n/a
29	chr17:46696077-46696127	HCF	heart:	n/a
30	chr17:46696077-46696127	Jurkat	blood:	n/a
31	chr17:46696077-46696127	SK-N-SH_RA	brain:	n/a
32	chr17:46696077-46696127	Hela-S3	cervix:	n/a
33	chr17:46696077-46696127	HIPEpiC	eye:	n/a
34	chr17:46696077-46696127	ECC-1	luminal epithelium:	n/a
35	chr17:46696077-46696127	AG04449	skin:	fetal
36	chr17:46696077-46696127	AG04450	lung:	fetal
37	chr17:46696077-46696127	BJ	skin:	n/a
38	chr17:46696077-46696127	HAEpiC	amniotic membrane:	n/a
39	chr17:46696077-46696127	GM12892	blood:	n/a
40	chr17:46696077-46696127	SAEC	small airway:	n/a
41	chr17:46696077-46696127	HPAEpiC	pulmonary alveolar:	n/a
42	chr17:46696077-46696127	HCT-116	colon:	n/a
43	chr17:46696077-46696127	HCPEpiC	choroid plexus:	n/a
44	chr17:46696077-46696127	MCF10A-Er-Src	breast:	n/a
45	chr17:46696077-46696127	PANC-1	pancreas:	n/a
46	chr17:46696077-46696127	SK-N-SH	brain:	n/a
47	chr17:46696077-46696127	GM12891	blood:	n/a
48	chr17:46696077-46696127	Caco-2	colon:	n/a
49	chr17:46696077-46696127	NH-A	brain:	n/a
50	chr17:46696077-46696127	GM12878	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:46694321..46697000-chr17:46864191..46866345,2	K562	blood:
2	chr17:46464628..46466806-chr17:46694501..46697277,2	K562	blood:
3	chr17:46102017..46103055-chr17:46695675..46696647,5	K562	blood:
4	chr17:46563248..46569374-chr17:46695616..46701359,7	K562	blood:
5	chr17:46384534..46385515-chr17:46695686..46696518,4	MCF-7	breast:
6	chr17:46212503..46213132-chr17:46695732..46696641,2	MCF-7	breast:
7	chr17:46681515..46685552-chr17:46695972..46700113,3	MCF-7	breast:
8	chr17:46333899..46335510-chr17:46695937..46698252,2	K562	blood:
9	chr17:46679707..46680548-chr17:46695663..46696342,3	MCF-7	breast:
10	chr17:46413747..46415915-chr17:46695597..46698773,3	K562	blood:
11	chr17:46694510..46697000-chr17:46702527..46704150,2	MCF-7	breast:
12	chr17:46679660..46680612-chr17:46695724..46696977,8	K562	blood:
13	chr17:46633214..46633990-chr17:46696005..46696512,2	K562	blood:
14	chr17:46102373..46103175-chr17:46695748..46696490,3	MCF-7	breast:
15	chr17:46408617..46416311-chr17:46693434..46699776,8	K562	blood:
16	chr17:46390188..46393069-chr17:46694762..46697606,2	K562	blood:
17	chr17:46429031..46429886-chr17:46695607..46696541,3	MCF-7	breast:
18	chr17:46625273..46627562-chr17:46694776..46697171,2	K562	blood:
19	chr17:46569833..46570442-chr17:46695977..46696577,2	K562	blood:
20	chr17:46463565..46466806-chr17:46694501..46697815,3	K562	blood:
21	chr17:46453134..46455609-chr17:46694822..46696897,2	K562	blood:
22	chr17:46413111..46413812-chr17:46695913..46696553,2	MCF-7	breast:
23	chr17:46679814..46680416-chr17:46695689..46696572,4	MCF-7	breast:
24	chr17:46429106..46429774-chr17:46695690..46696224,2	K562	blood:
25	chr17:46534407..46535828-chr17:46695754..46696608,3	K562	blood:
26	chr17:46206531..46208867-chr17:46695496..46698467,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALCOCO2-6	chr17:46694460-46696607	ENSG00000248304
2	lnc-HOXB9-1	chr17:46694457-46696602	NONHSAT054454

No data

Variant related genes	Relation type
HOXB8	TF binding region
HOXB8	CpG island
ENSG00000170689	Chromatin interaction
ENSG00000120093	Chromatin interaction
ENSG00000108511	Chromatin interaction
ENSG00000233101	Chromatin interaction
ENSG00000235300	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11079831	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16942777	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16942817	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2303489	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3096645	0.85[JPT][hapmap]
rs3096646	0.92[JPT][hapmap]
rs3744774	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3809777	0.88[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs3809778	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3826540	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3826541	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4619445	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs56347129	1.00[AFR][1000 genomes]
rs7405887	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs881012	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8844	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs890433	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs890434	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833469	chr17:46491849-46709406	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
2	esv3420538	chr17:46504944-46861553	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	369 gene(s)	inside rSNPs	diseases
3	nsv908577	chr17:46584900-46704536	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	343 gene(s)	inside rSNPs	diseases
4	nsv908578	chr17:46592413-46698710	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	335 gene(s)	inside rSNPs	diseases
5	nsv908579	chr17:46592413-46727289	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
6	nsv532113	chr17:46598247-47588570	Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	453 gene(s)	inside rSNPs	diseases
7	esv2758459	chr17:46602673-46836837	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	364 gene(s)	inside rSNPs	diseases
8	esv2758694	chr17:46602673-46836837	Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	364 gene(s)	inside rSNPs	diseases
9	nsv908580	chr17:46609103-46698710	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	335 gene(s)	inside rSNPs	diseases
10	nsv908581	chr17:46610646-46735520	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
11	nsv908582	chr17:46617019-46698710	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
12	nsv908583	chr17:46617019-46704536	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
13	nsv833471	chr17:46617787-46783345	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	356 gene(s)	inside rSNPs	diseases
14	nsv908584	chr17:46618926-46735520	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
15	nsv457822	chr17:46620402-46698710	Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
16	nsv575481	chr17:46620402-46698710	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
17	nsv457823	chr17:46620402-46704536	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
18	nsv575482	chr17:46620402-46704536	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
19	nsv543380	chr17:46686151-46721371	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46688600-46697000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
2	chr17:46689000-46698000	Bivalent/Poised TSS	Fetal Kidney	kidney
3	chr17:46693000-46696600	Enhancers	A549	lung
4	chr17:46693600-46696200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
5	chr17:46694600-46696600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
6	chr17:46694600-46697000	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr17:46694800-46696200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
8	chr17:46694800-46696600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
9	chr17:46694800-46697000	Bivalent Enhancer	Fetal Stomach	stomach
10	chr17:46695000-46696200	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr17:46695000-46696200	Bivalent Enhancer	Fetal Intestine Large	intestine
12	chr17:46695000-46696200	Bivalent Enhancer	Placenta	Placenta
13	chr17:46695000-46696400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
14	chr17:46695000-46696400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
15	chr17:46695000-46696400	Bivalent Enhancer	Colon Smooth Muscle	Colon
16	chr17:46695000-46696600	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr17:46695000-46696600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
18	chr17:46695000-46696600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
19	chr17:46695000-46696600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
20	chr17:46695000-46696600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
21	chr17:46695000-46696600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
22	chr17:46695000-46696800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
23	chr17:46695000-46697000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr17:46695000-46697000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr17:46695200-46696800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
26	chr17:46695400-46696200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr17:46695400-46696200	Bivalent Enhancer	NHLF	lung
28	chr17:46695400-46696400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
29	chr17:46695400-46696400	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
30	chr17:46695400-46696600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
31	chr17:46695600-46696200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
32	chr17:46695600-46696200	Bivalent Enhancer	Adipose Nuclei	Adipose
33	chr17:46695600-46696200	Bivalent Enhancer	HUVEC	blood vessel
34	chr17:46695600-46696400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
35	chr17:46695600-46696600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
36	chr17:46695600-46696600	Bivalent Enhancer	GM12878-XiMat	blood
37	chr17:46695600-46697400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
38	chr17:46695800-46696200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
39	chr17:46695800-46696400	Bivalent Enhancer	Liver	Liver
40	chr17:46695800-46696400	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr17:46695800-46696400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
42	chr17:46695800-46696600	Bivalent Enhancer	Colonic Mucosa	Colon
43	chr17:46695800-46697400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr17:46695800-46697400	Bivalent Enhancer	Fetal Lung	lung
45	chr17:46696000-46696200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr17:46696000-46696200	Bivalent Enhancer	Fetal Intestine Small	intestine
47	chr17:46696000-46696200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
48	chr17:46696000-46696200	Active TSS	Rectal Mucosa Donor 31	rectum
49	chr17:46696000-46696400	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr17:46696000-46696400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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