Variant report

Variant	rs61753571
Chromosome Location	chr1:85666344-85666345
allele	A/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	chr1:85666105-85667772	GM15510	blood:	n/a	n/a
2	CHD2	chr1:85666028-85667837	K562	blood:	n/a	n/a
3	POLR2A	chr1:85666199-85667934	K562	blood:	n/a	n/a
4	TCF3	chr1:85666184-85667306	GM12878	blood:	n/a	n/a
5	YY1	chr1:85666165-85667786	HepG2	liver:	n/a	chr1:85667352-85667361 chr1:85667364-85667378 chr1:85667561-85667575 chr1:85666800-85666809 chr1:85666979-85666993 chr1:85667361-85667375 chr1:85666771-85666785 chr1:85667358-85667367 chr1:85667364-85667373
6	HMGN3	chr1:85666087-85667819	K562	blood:	n/a	n/a
7	E2F6	chr1:85666188-85667934	K562	blood:	n/a	chr1:85666780-85666789 chr1:85667365-85667375 chr1:85667182-85667192
8	RCOR1	chr1:85666322-85667817	K562	blood:	n/a	n/a
9	MAX	chr1:85665831-85667904	HepG2	liver:	n/a	chr1:85667440-85667449 chr1:85667107-85667122 chr1:85667564-85667574
10	POLR2A	chr1:85666007-85667774	NB4	blood:	n/a	n/a
11	TBP	chr1:85665737-85667942	K562	blood:	n/a	chr1:85667404-85667415
12	E2F6	chr1:85666148-85667863	K562	blood:	n/a	chr1:85666780-85666789 chr1:85667365-85667375 chr1:85667182-85667192
13	SIN3AK20	chr1:85665636-85667932	PANC-1	pancreas:	n/a	n/a
14	MAX	chr1:85665919-85668042	H1-hESC	embryonic stem cell:	n/a	chr1:85667440-85667449 chr1:85667107-85667122 chr1:85667564-85667574
15	MAZ	chr1:85665873-85667882	K562	blood:	n/a	chr1:85667440-85667449 chr1:85667107-85667122 chr1:85667564-85667574
16	MYC	chr1:85666288-85666389	H1-hESC	embryonic stem cell:	n/a	n/a
17	ZBTB7A	chr1:85666130-85667868	ECC-1	luminal epithelium:	n/a	chr1:85667002-85667011
18	CREB1	chr1:85666067-85667848	HepG2	liver:	n/a	n/a
19	POLR2A	chr1:85666266-85666524	A549	lung:	n/a	n/a
20	ETS1	chr1:85665978-85667563	K562	blood:	n/a	chr1:85666803-85666814 chr1:85666775-85666786 chr1:85667356-85667367 chr1:85667362-85667373 chr1:85667350-85667361 chr1:85666749-85666760
21	E2F1	chr1:85666250-85667630	Hela-S3	cervix:	n/a	chr1:85666780-85666789 chr1:85666634-85666645 chr1:85667365-85667375 chr1:85667182-85667192
22	MAX	chr1:85666130-85668371	Hela-S3	cervix:	n/a	chr1:85667440-85667449 chr1:85668067-85668076 chr1:85667107-85667122 chr1:85667564-85667574
23	USF1	chr1:85666194-85666373	HepG2	liver:	n/a	n/a
24	BHLHE40	chr1:85666096-85667957	K562	blood:	n/a	chr1:85667358-85667374 chr1:85667142-85667158 chr1:85667177-85667193 chr1:85667163-85667179 chr1:85667107-85667120 chr1:85667171-85667187 chr1:85666769-85666785
25	TCF7L2	chr1:85665984-85668045	Hela-S3	cervix:	n/a	n/a
26	MAX	chr1:85665913-85668010	ECC-1	luminal epithelium:	n/a	chr1:85667440-85667449 chr1:85667107-85667122 chr1:85667564-85667574
27	TEAD4	chr1:85666282-85667921	ECC-1	luminal epithelium:	n/a	n/a
28	POLR2A	chr1:85665989-85667898	MCF-7	breast:	n/a	n/a
29	POLR2A	chr1:85666270-85667885	ProgFib	skin:	n/a	n/a
30	RCOR1	chr1:85665612-85667911	K562	blood:	n/a	n/a
31	MYC	chr1:85665807-85668385	K562	blood:	n/a	chr1:85667440-85667449 chr1:85668067-85668076 chr1:85667107-85667122 chr1:85667564-85667574
32	POLR2A	chr1:85666241-85668019	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr1:85665945-85667162	H1-neurons	neurons:	n/a	n/a
34	MTA3	chr1:85665795-85666368	GM12878	blood:	n/a	n/a
35	TCF3	chr1:85666332-85666494	GM12878	blood:	n/a	n/a
36	GABPA	chr1:85666300-85667021	K562	blood:	n/a	n/a
37	CBX3	chr1:85666284-85666990	K562	blood:	n/a	n/a
38	MAX	chr1:85666074-85667996	H1-hESC	embryonic stem cell:	n/a	chr1:85667440-85667449 chr1:85667107-85667122 chr1:85667564-85667574
39	BCLAF1	chr1:85666301-85666915	GM12878	blood:	n/a	chr1:85666767-85666780 chr1:85666802-85666811 chr1:85666748-85666757
40	HA-E2F1	chr1:85666191-85667702	Hela-S3	cervix:	n/a	chr1:85666780-85666789 chr1:85666634-85666645 chr1:85667365-85667375 chr1:85667182-85667192
41	ETS1	chr1:85666070-85667240	K562	blood:	n/a	chr1:85666803-85666814 chr1:85666775-85666786 chr1:85666749-85666760
42	POLR2A	chr1:85665706-85668876	PANC-1	pancreas:	n/a	n/a
43	HEY1	chr1:85666332-85667523	K562	blood:	n/a	chr1:85666986-85667001 chr1:85666977-85666992
44	SIN3AK20	chr1:85665906-85667529	K562	blood:	n/a	n/a
45	MXI1	chr1:85665970-85667995	Hela-S3	cervix:	n/a	n/a
46	USF1	chr1:85666174-85667569	ECC-1	luminal epithelium:	n/a	chr1:85667358-85667374 chr1:85667142-85667158 chr1:85667177-85667193 chr1:85667163-85667179 chr1:85667107-85667120 chr1:85667171-85667187 chr1:85666769-85666785 chr1:85667057-85667068
47	TCF7L2	chr1:85666226-85666983	HEK293	kidney:	n/a	n/a
48	POLR2A	chr1:85666196-85667759	GM12878	blood:	n/a	n/a
49	MAX	chr1:85665799-85668100	A549	lung:	n/a	chr1:85667440-85667449 chr1:85668067-85668076 chr1:85667107-85667122 chr1:85667564-85667574
50	TAF1	chr1:85666053-85667731	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:85664620..85668785-chr1:85722586..85726821,6	MCF-7	breast:
2	chr1:85665631..85669772-chr1:85739485..85744059,5	K562	blood:
3	chr1:85665831..85667640-chr1:86041122..86042846,2	MCF-7	breast:
4	chr1:85666179..85667836-chr1:85723614..85725791,2	K562	blood:
5	chr1:85665227..85667257-chr1:85740935..85743875,2	K562	blood:
6	chr1:85597874..85599552-chr1:85665218..85666801,2	MCF-7	breast:
7	chr1:85665913..85668656-chr1:85741362..85743092,3	MCF-7	breast:

Variant related genes	Relation type
SYDE2	TF binding region
ENSG00000142867	Chromatin interaction
ENSG00000162642	Chromatin interaction
ENSG00000153904	Chromatin interaction
ENSG00000266110	Chromatin interaction
ENSG00000223653	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11161540	1.00[AMR][1000 genomes]
rs11161568	1.00[EUR][1000 genomes]
rs12065571	1.00[AMR][1000 genomes]
rs12070991	1.00[AMR][1000 genomes]
rs12084022	1.00[AMR][1000 genomes]
rs12090608	1.00[AMR][1000 genomes]
rs1554596	1.00[EUR][1000 genomes]
rs17121967	1.00[EUR][1000 genomes]
rs17122190	1.00[AMR][1000 genomes]
rs58278399	1.00[EUR][1000 genomes]
rs59078755	1.00[EUR][1000 genomes]
rs61753572	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61753619	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6656799	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6663475	1.00[AMR][1000 genomes]
rs6664025	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6664273	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6667700	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6670564	1.00[EUR][1000 genomes]
rs72952681	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv34165	chr1:85542040-85846249	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv830459	chr1:85589585-85786311	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription 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 miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	esv1792086	chr1:85644478-85667608	Strong transcription Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
5	nsv546701	chr1:85662851-85667386	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
6	nsv546702	chr1:85663699-85667356	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
7	esv1800754	chr1:85663699-85667557	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	esv1801195	chr1:85663699-85667608	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
9	esv1811802	chr1:85663699-85667608	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
10	esv1812785	chr1:85663699-85667608	Enhancers Bivalent/Poised TSS Weak transcription Active TSS 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	7 gene(s)	inside rSNPs	diseases
11	esv3324235	chr1:85665789-85668337	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
12	esv1836892	chr1:85666118-85667608	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
13	esv3325481	chr1:85666189-85668737	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
14	esv17132	chr1:85666191-85667696	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
15	nsv546703	chr1:85666270-85667130	Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
16	nsv546704	chr1:85666270-85667188	Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
17	nsv546705	chr1:85666270-85667246	Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
18	nsv546706	chr1:85666270-85667305	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
19	nsv546707	chr1:85666270-85667356	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
20	esv1835548	chr1:85666270-85667386	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
21	esv1800540	chr1:85666270-85667557	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
22	esv1806962	chr1:85666270-85667557	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
23	esv1812840	chr1:85666270-85667557	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
24	esv1816636	chr1:85666270-85667557	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
25	esv1827813	chr1:85666270-85667557	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
26	esv1833642	chr1:85666270-85667557	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
27	esv1838789	chr1:85666270-85667557	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
28	nsv546708	chr1:85666270-85667557	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
29	esv1793256	chr1:85666270-85667608	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
30	esv1812447	chr1:85666270-85667608	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
31	esv1815225	chr1:85666270-85667608	Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
32	esv1818170	chr1:85666270-85667608	Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
33	esv1826943	chr1:85666270-85667608	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
34	esv1838733	chr1:85666270-85667608	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
35	nsv546709	chr1:85666270-85667608	Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85661000-85669000	Active TSS	Stomach Smooth Muscle	stomach
2	chr1:85661400-85668400	Active TSS	Colon Smooth Muscle	Colon
3	chr1:85663600-85666400	Active TSS	Right Atrium	heart
4	chr1:85663600-85668600	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr1:85663800-85667600	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr1:85663800-85667800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:85663800-85667800	Active TSS	K562	blood
8	chr1:85663800-85668000	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr1:85663800-85668200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:85663800-85668200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:85663800-85668600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:85664000-85667800	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr1:85664000-85668200	Active TSS	Fetal Intestine Large	intestine
14	chr1:85664200-85667600	Active TSS	HMEC	breast
15	chr1:85664400-85668200	Active TSS	Fetal Kidney	kidney
16	chr1:85664600-85666400	Active TSS	Fetal Heart	heart
17	chr1:85664600-85667200	Active TSS	Colonic Mucosa	Colon
18	chr1:85664600-85667800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:85664600-85667800	Active TSS	NHLF	lung
20	chr1:85664600-85668000	Active TSS	Fetal Intestine Small	intestine
21	chr1:85664600-85668400	Active TSS	H1 Cell Line	embryonic stem cell
22	chr1:85664600-85668400	Active TSS	Aorta	Aorta
23	chr1:85664800-85668200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:85664800-85668200	Active TSS	Breast Myoepithelial Primary Cells	Breast
25	chr1:85664800-85668200	Active TSS	A549	lung
26	chr1:85665000-85668000	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr1:85665000-85668000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:85665200-85667600	Active TSS	NHEK	skin
29	chr1:85665200-85668000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr1:85665200-85668000	Active TSS	H9 Cell Line	embryonic stem cell
31	chr1:85665200-85668000	Active TSS	Ovary	ovary
32	chr1:85665200-85668000	Active TSS	GM12878-XiMat	blood
33	chr1:85665200-85668200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr1:85665200-85668600	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr1:85665400-85667600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:85665400-85667600	Bivalent Enhancer	Fetal Brain Male	brain
37	chr1:85665400-85667800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr1:85665400-85667800	Bivalent/Poised TSS	HepG2	liver
39	chr1:85665400-85667800	Active TSS	HSMMtube	muscle
40	chr1:85665400-85668000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr1:85665400-85668000	Active TSS	Psoas Muscle	Psoas
42	chr1:85665400-85668000	Active TSS	Stomach Mucosa	stomach
43	chr1:85665400-85668000	Bivalent/Poised TSS	Thymus	Thymus
44	chr1:85665400-85668200	Active TSS	NHDF-Ad	bronchial
45	chr1:85665400-85668400	Active TSS	Left Ventricle	heart
46	chr1:85665600-85666800	Active TSS	Brain Hippocampus Middle	brain
47	chr1:85665600-85667000	Active TSS	Brain Substantia Nigra	brain
48	chr1:85665600-85667400	Active TSS	Brain Inferior Temporal Lobe	brain
49	chr1:85665600-85667600	Active TSS	Brain Angular Gyrus	brain
50	chr1:85665600-85667600	Active TSS	Brain Anterior Caudate	brain

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