Variant report

Variant	rs35808545
Chromosome Location	chr17:37774254-37774255
allele	-/C
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	POLR2A	chr17:37773914-37774416	HUVEC	blood vessel:	n/a	n/a
2	MYC	chr17:37773876-37774919	Hela-S3	cervix:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37774889-37774899 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
3	TCF12	chr17:37773658-37774436	ECC-1	luminal epithelium:	n/a	n/a
4	BHLHE40	chr17:37773952-37774258	HepG2	liver:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
5	E2F6	chr17:37773801-37774463	K562	blood:	n/a	chr17:37774171-37774182 chr17:37774198-37774207 chr17:37774140-37774154 chr17:37774374-37774388
6	CTCF	chr17:37774140-37774290	GM12865	blood:	n/a	n/a
7	MXI1	chr17:37773375-37775120	SK-N-SH	brain:	n/a	n/a
8	POLR2A	chr17:37773840-37774850	NB4	blood:	n/a	n/a
9	USF1	chr17:37773964-37774317	SK-N-SH	brain:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
10	E2F6	chr17:37773895-37774452	A549	lung:	n/a	chr17:37774171-37774182 chr17:37774198-37774207 chr17:37774140-37774154 chr17:37774374-37774388
11	MAZ	chr17:37773548-37775040	IMR90	lung:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37774889-37774899 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
12	HA-E2F1	chr17:37773607-37774320	MCF-7	breast:	n/a	chr17:37774198-37774207 chr17:37774140-37774154
13	MAX	chr17:37773837-37774579	H1-hESC	embryonic stem cell:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
14	MYC	chr17:37774052-37774428	HUVEC	blood vessel:	n/a	chr17:37774166-37774176 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
15	ZBTB7A	chr17:37774014-37774704	K562	blood:	n/a	n/a
16	POLR2A	chr17:37774242-37774403	A549	lung:	n/a	n/a
17	MAX	chr17:37773752-37774609	ECC-1	luminal epithelium:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
18	ELF1	chr17:37773877-37774297	K562	blood:	n/a	n/a
19	MAX	chr17:37773933-37774413	H1-hESC	embryonic stem cell:	n/a	chr17:37774166-37774176 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
20	MYC	chr17:37773715-37775034	NB4	blood:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37774889-37774899 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
21	MAX	chr17:37773466-37775262	A549	lung:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37774889-37774899 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
22	CREB1	chr17:37773877-37774555	A549	lung:	n/a	n/a
23	POLR2A	chr17:37773921-37774405	ECC-1	luminal epithelium:	n/a	n/a
24	CHD2	chr17:37773880-37774372	Hela-S3	cervix:	n/a	n/a
25	MAX	chr17:37773534-37774498	K562	blood:	n/a	chr17:37774166-37774176 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
26	EP300	chr17:37773695-37774490	ECC-1	luminal epithelium:	n/a	chr17:37774176-37774192
27	MXI1	chr17:37773761-37775068	IMR90	lung:	n/a	n/a
28	ZNF143	chr17:37773533-37774295	GM12878	blood:	n/a	n/a
29	MAX	chr17:37773895-37774775	A549	lung:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
30	POLR2A	chr17:37773974-37774408	Hela-S3	cervix:	n/a	n/a
31	BHLHE40	chr17:37773917-37774311	A549	lung:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
32	JUND	chr17:37773904-37774436	A549	lung:	n/a	chr17:37774199-37774208
33	POLR2A	chr17:37773930-37774415	HCT-116	colon:	n/a	n/a
34	BHLHE40	chr17:37773696-37774351	GM12878	blood:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
35	HA-E2F1	chr17:37773852-37774634	Hela-S3	cervix:	n/a	chr17:37774198-37774207 chr17:37774140-37774154 chr17:37774374-37774388
36	E2F6	chr17:37773820-37775024	A549	lung:	n/a	chr17:37774171-37774182 chr17:37774198-37774207 chr17:37774891-37774903 chr17:37774140-37774154 chr17:37774374-37774388
37	MAX	chr17:37773867-37774579	SK-N-SH	brain:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
38	YY1	chr17:37773874-37774779	ECC-1	luminal epithelium:	n/a	chr17:37774165-37774174 chr17:37774507-37774521 chr17:37774581-37774589
39	TEAD4	chr17:37773884-37774856	ECC-1	luminal epithelium:	n/a	n/a
40	TAF1	chr17:37774166-37774432	SK-N-SH	brain:	n/a	n/a
41	MAX	chr17:37773980-37774466	HepG2	liver:	n/a	chr17:37774166-37774176 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
42	USF1	chr17:37773871-37774334	A549	lung:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
43	MAX	chr17:37773764-37775308	ECC-1	luminal epithelium:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37774889-37774899 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
44	BHLHE40	chr17:37773888-37774303	K562	blood:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
45	POLR2A	chr17:37774014-37774375	MCF10A-Er-Src	breast:	n/a	n/a
46	MAX	chr17:37773924-37774572	SK-N-SH	brain:	n/a	chr17:37774548-37774558 chr17:37774166-37774176 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
47	MXI1	chr17:37773961-37774389	Hela-S3	cervix:	n/a	n/a
48	MAX	chr17:37773581-37774963	NB4	blood:	n/a	chr17:37774569-37774579 chr17:37774548-37774558 chr17:37774166-37774176 chr17:37774889-37774899 chr17:37773959-37773969 chr17:37774398-37774407 chr17:37774297-37774306 chr17:37774115-37774126
49	POLR2A	chr17:37773914-37774419	HL-60	blood:	n/a	n/a
50	TEAD4	chr17:37773951-37774591	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37774242-37774292	PrEC	prostate:	n/a
2	chr17:37774242-37774292	HPAEpiC	pulmonary alveolar:	n/a
3	chr17:37774242-37774292	GM12891	blood:	n/a
4	chr17:37774242-37774292	LNCaP	prostate:	n/a
5	chr17:37774242-37774292	AG09319	gingival:	n/a
6	chr17:37774242-37774292	HIPEpiC	eye:	n/a
7	chr17:37774242-37774292	CMK	blood:	n/a
8	chr17:37774242-37774292	IMR90	lung:	fetal
9	chr17:37774242-37774292	U87	brain:	n/a
10	chr17:37774242-37774292	Hepatocyte	liver:	n/a
11	chr17:37774242-37774292	HCPEpiC	choroid plexus:	n/a
12	chr17:37774242-37774292	GM06990	blood:	n/a
13	chr17:37774242-37774292	HEK293	kidney:	embryo
14	chr17:37774242-37774292	K562	blood:	n/a
15	chr17:37774242-37774292	ovcar-3	ovarian:	n/a
16	chr17:37774242-37774292	H1-hESC	embryonic stem cell:	embryo
17	chr17:37774242-37774292	ECC-1	luminal epithelium:	n/a
18	chr17:37774242-37774292	HAEpiC	amniotic membrane:	n/a
19	chr17:37774242-37774292	HMEC	breast:	n/a
20	chr17:37774242-37774292	NHDF-neo	bronchial:	n/a
21	chr17:37774242-37774292	SAEC	small airway:	n/a
22	chr17:37774242-37774292	T-47D	breast:	n/a
23	chr17:37774242-37774292	AG10803	skin:	n/a
24	chr17:37774242-37774292	NHBE	bronchial:	n/a
25	chr17:37774242-37774292	PFSK-1	brain:	n/a
26	chr17:37774242-37774292	MCF10A-Er-Src	breast:	n/a
27	chr17:37774242-37774292	HRPEpiC	eye:	n/a
28	chr17:37774242-37774292	PANC-1	pancreas:	n/a
29	chr17:37774242-37774292	HCF	heart:	n/a
30	chr17:37774242-37774292	RPTEC	kidney:	n/a
31	chr17:37774242-37774292	SK-N-SH_RA	brain:	n/a
32	chr17:37774242-37774292	GM19239	blood:	n/a
33	chr17:37774242-37774292	A549	lung:	n/a
34	chr17:37774242-37774292	AoSMC	blood vessel:	n/a
35	chr17:37774242-37774292	ProgFib	skin:	n/a
36	chr17:37774242-37774292	NB4	blood:	n/a
37	chr17:37774242-37774292	AG04450	lung:	fetal
38	chr17:37774242-37774292	SKMC	muscle:	n/a
39	chr17:37774242-37774292	HRCEpiC	kidney:	n/a
40	chr17:37774242-37774292	HCT-116	colon:	n/a
41	chr17:37774242-37774292	Jurkat	blood:	n/a
42	chr17:37774242-37774292	HUVEC	blood vessel:	n/a
43	chr17:37774242-37774292	BJ	skin:	n/a
44	chr17:37774242-37774292	NH-A	brain:	n/a
45	chr17:37774242-37774292	HepG2	liver:	n/a
46	chr17:37774242-37774292	NT2-D1	testis:	n/a
47	chr17:37774242-37774292	AG09309	skin:	n/a
48	chr17:37774242-37774292	Caco-2	colon:	n/a
49	chr17:37774242-37774292	GM12878	blood:	n/a
50	chr17:37774242-37774292	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:37772840..37775144-chr17:37791860..37794775,2	MCF-7	breast:
2	chr17:37769144..37771005-chr17:37773634..37775729,2	MCF-7	breast:
3	chr17:37768363..37771309-chr17:37772118..37774468,3	K562	blood:
4	chr17:37758356..37760181-chr17:37774194..37775834,2	MCF-7	breast:
5	chr17:37763822..37767125-chr17:37772337..37774939,3	MCF-7	breast:
6	chr17:37773896..37776239-chr17:37886682..37888820,2	MCF-7	breast:
7	chr17:37773259..37775797-chr17:37912370..37914095,2	MCF-7	breast:
8	chr17:37356113..37357004-chr17:37773849..37774768,2	NB4	blood:
9	chr17:37730305..37732141-chr17:37773715..37775844,2	MCF-7	breast:
10	chr17:37773404..37776321-chr17:37819728..37822241,2	MCF-7	breast:
11	chr17:37773726..37775508-chr17:37899665..37902639,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000214546	TF binding region
ENSG00000214546	CpG island
ENSG00000171532	Chromatin interaction
ENSG00000141741	Chromatin interaction
ENSG00000173991	Chromatin interaction
ENSG00000108298	Chromatin interaction
ENSG00000131748	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription 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	92 gene(s)	inside rSNPs	diseases
2	nsv1066033	chr17:37333956-37795617	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers 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	78 gene(s)	inside rSNPs	diseases
3	nsv543340	chr17:37333956-37795617	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases
4	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
5	nsv833442	chr17:37692880-37861291	Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
6	nsv521294	chr17:37694709-37804858	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv908205	chr17:37709422-37830900	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv908206	chr17:37709422-37866005	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
9	nsv908207	chr17:37709422-37922259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
10	nsv833443	chr17:37725640-37882864	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
11	nsv908208	chr17:37749259-37781849	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
12	nsv908209	chr17:37749259-37790340	Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
13	nsv908210	chr17:37761202-37781849	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv908211	chr17:37765047-37782410	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	nsv908212	chr17:37765047-37790340	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
16	nsv457738	chr17:37770005-37831035	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
17	nsv574991	chr17:37770005-37831035	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
18	esv3391098	chr17:37773251-37775799	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37771800-37776200	Enhancers	Fetal Brain Male	brain
2	chr17:37773400-37775200	Bivalent/Poised TSS	NHEK	skin
3	chr17:37773600-37774600	Bivalent/Poised TSS	Thymus	Thymus
4	chr17:37773600-37774600	Active TSS	K562	blood
5	chr17:37773600-37774800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
6	chr17:37773600-37774800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr17:37773600-37775000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
8	chr17:37773600-37775200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr17:37773600-37775200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
10	chr17:37773600-37775200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
11	chr17:37773600-37775200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
12	chr17:37773600-37775200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
13	chr17:37773600-37775200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr17:37773600-37775200	Enhancers	Liver	Liver
15	chr17:37773800-37774600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
16	chr17:37773800-37774600	Bivalent/Poised TSS	HepG2	liver
17	chr17:37773800-37774600	Active TSS	HUVEC	blood vessel
18	chr17:37773800-37774800	Active TSS	Primary T cells from cord blood	blood
19	chr17:37773800-37774800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr17:37773800-37774800	Active TSS	Rectal Mucosa Donor 29	rectum
21	chr17:37773800-37775000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
22	chr17:37773800-37775000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr17:37773800-37775000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr17:37773800-37775000	Active TSS	Aorta	Aorta
25	chr17:37773800-37775000	Active TSS	Colon Smooth Muscle	Colon
26	chr17:37773800-37775000	Active TSS	Esophagus	oesophagus
27	chr17:37773800-37775000	Active TSS	Gastric	stomach
28	chr17:37773800-37775000	Active TSS	Left Ventricle	heart
29	chr17:37773800-37775200	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr17:37773800-37775200	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr17:37773800-37775200	Enhancers	Fetal Lung	lung
32	chr17:37773800-37775200	Active TSS	Lung	lung
33	chr17:37773800-37775200	Active TSS	Rectal Smooth Muscle	rectum
34	chr17:37773800-37775200	Bivalent/Poised TSS	NHLF	lung
35	chr17:37773800-37775400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr17:37773800-37775400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
37	chr17:37774000-37774600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:37774000-37774600	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr17:37774000-37774600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr17:37774000-37774600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr17:37774000-37774600	Active TSS	Primary B cells from cord blood	blood
42	chr17:37774000-37774600	Active TSS	Primary B cells from peripheral blood	blood
43	chr17:37774000-37774600	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
44	chr17:37774000-37774600	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr17:37774000-37774600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr17:37774000-37774600	Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr17:37774000-37774600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr17:37774000-37774600	Active TSS	Primary T helper cells fromperipheralblood	blood
49	chr17:37774000-37774600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr17:37774000-37774600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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