Variant report

Variant	rs547933388
Chromosome Location	chr17:37774758-37774759
allele	A/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	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
2	POLR2A	chr17:37774697-37775019	Hela-S3	cervix:	n/a	n/a
3	MXI1	chr17:37773375-37775120	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr17:37773840-37774850	NB4	blood:	n/a	n/a
5	EP300	chr17:37774616-37775314	A549	lung:	n/a	n/a
6	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
7	POU2F2	chr17:37774461-37774815	GM12891	blood:	n/a	chr17:37774701-37774710 chr17:37774710-37774717 chr17:37774724-37774739 chr17:37774709-37774719 chr17:37774696-37774714 chr17:37774709-37774717 chr17:37774708-37774718 chr17:37774700-37774712 chr17:37774706-37774720 chr17:37774706-37774721 chr17:37774709-37774719 chr17:37774702-37774723 chr17:37774718-37774733 chr17:37774700-37774710 chr17:37774709-37774718 chr17:37774704-37774722 chr17:37774702-37774709 chr17:37774708-37774720 chr17:37774702-37774724 chr17:37774707-37774718 chr17:37774707-37774720
8	POU2F2	chr17:37774548-37774840	GM12878	blood:	n/a	chr17:37774701-37774710 chr17:37774710-37774717 chr17:37774724-37774739 chr17:37774709-37774719 chr17:37774696-37774714 chr17:37774709-37774717 chr17:37774708-37774718 chr17:37774700-37774712 chr17:37774706-37774720 chr17:37774706-37774721 chr17:37774709-37774719 chr17:37774702-37774723 chr17:37774718-37774733 chr17:37774700-37774710 chr17:37774709-37774718 chr17:37774704-37774722 chr17:37774702-37774709 chr17:37774708-37774720 chr17:37774702-37774724 chr17:37774707-37774718 chr17:37774707-37774720
9	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
10	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
11	REST	chr17:37774470-37774881	A549	lung:	n/a	chr17:37774569-37774582
12	MXI1	chr17:37773761-37775068	IMR90	lung:	n/a	n/a
13	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
14	YY1	chr17:37774472-37775146	H1-hESC	embryonic stem cell:	n/a	chr17:37774902-37774913 chr17:37774507-37774521 chr17:37774581-37774589
15	MAFK	chr17:37774670-37774941	Hela-S3	cervix:	n/a	n/a
16	E2F6	chr17:37773820-37775024	A549	lung:	n/a	chr17:37774171-37774182 chr17:37774198-37774207 chr17:37774891-37774903 chr17:37774140-37774154 chr17:37774374-37774388
17	YY1	chr17:37773874-37774779	ECC-1	luminal epithelium:	n/a	chr17:37774165-37774174 chr17:37774507-37774521 chr17:37774581-37774589
18	TEAD4	chr17:37773884-37774856	ECC-1	luminal epithelium:	n/a	n/a
19	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
20	POLR2A	chr17:37774581-37774985	Hela-S3	cervix:	n/a	n/a
21	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
22	POU2F2	chr17:37774544-37774770	GM12878	blood:	n/a	chr17:37774701-37774710 chr17:37774710-37774717 chr17:37774724-37774739 chr17:37774709-37774719 chr17:37774696-37774714 chr17:37774709-37774717 chr17:37774708-37774718 chr17:37774700-37774712 chr17:37774706-37774720 chr17:37774706-37774721 chr17:37774709-37774719 chr17:37774702-37774723 chr17:37774718-37774733 chr17:37774700-37774710 chr17:37774709-37774718 chr17:37774704-37774722 chr17:37774702-37774709 chr17:37774708-37774720 chr17:37774702-37774724 chr17:37774707-37774718 chr17:37774707-37774720
23	POU2F2	chr17:37774525-37774937	GM12878	blood:	n/a	chr17:37774701-37774710 chr17:37774710-37774717 chr17:37774724-37774739 chr17:37774709-37774719 chr17:37774696-37774714 chr17:37774709-37774717 chr17:37774708-37774718 chr17:37774700-37774712 chr17:37774706-37774720 chr17:37774706-37774721 chr17:37774709-37774719 chr17:37774702-37774723 chr17:37774718-37774733 chr17:37774700-37774710 chr17:37774709-37774718 chr17:37774704-37774722 chr17:37774702-37774709 chr17:37774708-37774720 chr17:37774702-37774724 chr17:37774707-37774718 chr17:37774707-37774720
24	YY1	chr17:37774578-37774830	SK-N-SH_RA	brain:	n/a	chr17:37774581-37774589
25	RFX5	chr17:37774629-37775071	Hela-S3	cervix:	n/a	n/a
26	HA-E2F1	chr17:37774612-37775127	MCF-7	breast:	n/a	chr17:37774891-37774903
27	SP1	chr17:37774027-37775043	A549	lung:	n/a	chr17:37774506-37774518 chr17:37774278-37774285 chr17:37774569-37774583 chr17:37774508-37774517
28	STAT3	chr17:37774675-37774875	MCF10A-Er-Src	breast:	n/a	n/a
29	NFIC	chr17:37773511-37775157	ECC-1	luminal epithelium:	n/a	n/a
30	MYC	chr17:37773778-37775142	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
31	ZNF143	chr17:37774736-37774873	Hela-S3	cervix:	n/a	n/a
32	MAX	chr17:37774626-37775315	ECC-1	luminal epithelium:	n/a	chr17:37774889-37774899
33	ARID3A	chr17:37774705-37774830	HepG2	liver:	n/a	chr17:37774718-37774734 chr17:37774719-37774735
34	MAX	chr17:37773580-37775345	HCT-116	colon:	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
35	MYC	chr17:37773957-37774962	MCF10A-Er-Src	breast:	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
36	MXI1	chr17:37774639-37775203	Hela-S3	cervix:	n/a	chr17:37775159-37775174
37	MAX	chr17:37773322-37775248	HCT-116	colon:	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
38	MAX	chr17:37774667-37775132	SK-N-SH	brain:	n/a	chr17:37774889-37774899
39	SIN3A	chr17:37774674-37774877	H1-hESC	embryonic stem cell:	n/a	n/a
40	SP1	chr17:37773857-37775078	A549	lung:	n/a	chr17:37775065-37775074 chr17:37774506-37774518 chr17:37774278-37774285 chr17:37774569-37774583 chr17:37774508-37774517
41	MYC	chr17:37774604-37774789	K562	blood:	n/a	n/a
42	TCF12	chr17:37774411-37775176	A549	lung:	n/a	n/a
43	NFIC	chr17:37773546-37775082	ECC-1	luminal epithelium:	n/a	n/a
44	POLR2A	chr17:37773781-37775096	Hela-S3	cervix:	n/a	n/a
45	MAZ	chr17:37773704-37775020	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
46	E2F4	chr17:37774623-37775055	MCF10A-Er-Src	breast:	n/a	chr17:37774891-37774903
47	MYC	chr17:37773495-37775042	MCF10A-Er-Src	breast:	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
48	REST	chr17:37774513-37774794	A549	lung:	n/a	chr17:37774569-37774582
49	MAX	chr17:37773369-37775395	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
50	MAX	chr17:37773671-37775161	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

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	chr17:37774543..37777330-chr17:37885224..37887436,2	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
ENSG00000173991	Chromatin interaction
ENSG00000171532	Chromatin interaction
ENSG00000108298	Chromatin interaction
ENSG00000141741	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:124 , 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	chr17:37773600-37774800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
4	chr17:37773600-37774800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
5	chr17:37773600-37775000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
6	chr17:37773600-37775200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr17:37773600-37775200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
8	chr17:37773600-37775200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
9	chr17:37773600-37775200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr17:37773600-37775200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
11	chr17:37773600-37775200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr17:37773600-37775200	Enhancers	Liver	Liver
13	chr17:37773800-37774800	Active TSS	Primary T cells from cord blood	blood
14	chr17:37773800-37774800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr17:37773800-37774800	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr17:37773800-37775000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
17	chr17:37773800-37775000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr17:37773800-37775000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr17:37773800-37775000	Active TSS	Aorta	Aorta
20	chr17:37773800-37775000	Active TSS	Colon Smooth Muscle	Colon
21	chr17:37773800-37775000	Active TSS	Esophagus	oesophagus
22	chr17:37773800-37775000	Active TSS	Gastric	stomach
23	chr17:37773800-37775000	Active TSS	Left Ventricle	heart
24	chr17:37773800-37775200	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr17:37773800-37775200	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr17:37773800-37775200	Enhancers	Fetal Lung	lung
27	chr17:37773800-37775200	Active TSS	Lung	lung
28	chr17:37773800-37775200	Active TSS	Rectal Smooth Muscle	rectum
29	chr17:37773800-37775200	Bivalent/Poised TSS	NHLF	lung
30	chr17:37773800-37775400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr17:37773800-37775400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
32	chr17:37774000-37774800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr17:37774000-37774800	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr17:37774000-37774800	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr17:37774000-37774800	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr17:37774000-37774800	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr17:37774000-37774800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr17:37774000-37774800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr17:37774000-37774800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr17:37774000-37774800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr17:37774000-37774800	Active TSS	Brain Hippocampus Middle	brain
42	chr17:37774000-37774800	Active TSS	Colonic Mucosa	Colon
43	chr17:37774000-37774800	Active TSS	Duodenum Mucosa	Duodenum
44	chr17:37774000-37774800	Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr17:37774000-37774800	Active TSS	Fetal Brain Female	brain
46	chr17:37774000-37774800	Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr17:37774000-37774800	Active TSS	Small Intestine	intestine
48	chr17:37774000-37774800	Active TSS	A549	lung
49	chr17:37774000-37774800	Active TSS	HMEC	breast
50	chr17:37774000-37775000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell

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