Variant report

Variant	rs2396755
Chromosome Location	chr7:100487520-100487521
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:339)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:339 , 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	MYBL2	chr7:100487356-100488099	HepG2	liver:	n/a	n/a
2	POLR2A	chr7:100484343-100487721	HL-60	blood:	n/a	n/a
3	POLR2A	chr7:100482512-100488569	K562	blood:	n/a	n/a
4	POLR2A	chr7:100487389-100487731	A549	lung:	n/a	n/a
5	HEY1	chr7:100487384-100487679	HepG2	liver:	n/a	n/a
6	ETS1	chr7:100487387-100487793	A549	lung:	n/a	n/a
7	TBP	chr7:100486896-100488252	H1-hESC	embryonic stem cell:	n/a	n/a
8	MAX	chr7:100486798-100488360	ECC-1	luminal epithelium:	n/a	chr7:100487090-100487099 chr7:100487091-100487101
9	SIN3AK20	chr7:100486306-100487861	PANC-1	pancreas:	n/a	n/a
10	FOXM1	chr7:100487412-100487790	GM12878	blood:	n/a	n/a
11	MXI1	chr7:100486055-100488667	IMR90	lung:	n/a	chr7:100487091-100487100
12	UBTF	chr7:100486100-100488487	K562	blood:	n/a	n/a
13	REST	chr7:100486797-100487742	A549	lung:	n/a	chr7:100487063-100487072 chr7:100486961-100486968 chr7:100487155-100487162
14	PAX5	chr7:100486720-100487668	GM12892	blood:	n/a	chr7:100487196-100487205
15	MYC	chr7:100485082-100488580	NB4	blood:	n/a	chr7:100487090-100487099 chr7:100487091-100487101 chr7:100485503-100485513
16	HEY1	chr7:100487391-100488242	K562	blood:	n/a	n/a
17	POLR2A	chr7:100486444-100488181	GM10847	blood:	n/a	n/a
18	ZBTB7A	chr7:100487386-100488989	K562	blood:	n/a	n/a
19	PML	chr7:100486432-100488427	MCF-7	breast:	n/a	n/a
20	ZNF263	chr7:100487493-100488223	HEK293-T-REx	kidney:	n/a	n/a
21	ZBTB7A	chr7:100487404-100488720	ECC-1	luminal epithelium:	n/a	n/a
22	NRF1	chr7:100486876-100488328	SK-N-SH	brain:	n/a	chr7:100487442-100487453 chr7:100487442-100487453 chr7:100487439-100487453
23	POLR2A	chr7:100484695-100488620	PANC-1	pancreas:	n/a	n/a
24	ZBTB7A	chr7:100487369-100489176	K562	blood:	n/a	n/a
25	MYC	chr7:100486805-100487556	K562	blood:	n/a	chr7:100487090-100487099 chr7:100487091-100487101
26	MAX	chr7:100486267-100488891	MCF-7	breast:	n/a	chr7:100487090-100487099 chr7:100487091-100487101
27	POLR2A	chr7:100480317-100488960	GM12878	blood:	n/a	n/a
28	POLR2A	chr7:100487384-100487733	A549	lung:	n/a	n/a
29	USF1	chr7:100487377-100487638	SK-N-SH_RA	brain:	n/a	n/a
30	POLR2A	chr7:100487009-100487608	HepG2	liver:	n/a	n/a
31	MAX	chr7:100486650-100488443	A549	lung:	n/a	chr7:100487090-100487099 chr7:100487091-100487101
32	POLR2A	chr7:100486133-100488727	HUVEC	blood vessel:	n/a	n/a
33	REST	chr7:100487388-100487728	SK-N-SH	brain:	n/a	n/a
34	TBP	chr7:100487133-100487607	HepG2	liver:	n/a	n/a
35	MXI1	chr7:100486883-100488201	Hela-S3	cervix:	n/a	chr7:100487091-100487100
36	ZNF143	chr7:100487066-100487673	GM12878	blood:	n/a	n/a
37	ESRRA	chr7:100486584-100489049	GM12878	blood:	n/a	n/a
38	TAF1	chr7:100487384-100488647	MCF-7	breast:	n/a	n/a
39	RCOR1	chr7:100487464-100488096	GM12878	blood:	n/a	n/a
40	RCOR1	chr7:100487279-100488047	Hela-S3	cervix:	n/a	n/a
41	POU2F2	chr7:100487416-100487718	GM12878	blood:	n/a	chr7:100487435-100487447 chr7:100487534-100487546
42	E2F4	chr7:100487406-100487620	MCF10A-Er-Src	breast:	n/a	chr7:100487443-100487452
43	MAX	chr7:100486220-100488472	A549	lung:	n/a	chr7:100487090-100487099 chr7:100487091-100487101
44	NRF1	chr7:100487251-100487642	H1-hESC	embryonic stem cell:	n/a	chr7:100487442-100487453 chr7:100487442-100487453 chr7:100487439-100487453
45	REST	chr7:100487385-100487696	SK-N-SH	brain:	n/a	n/a
46	MXI1	chr7:100486890-100487633	HepG2	liver:	n/a	chr7:100487091-100487100
47	POLR2A	chr7:100484558-100487869	GM18505	blood:	n/a	n/a
48	MAX	chr7:100486849-100487626	HepG2	liver:	n/a	chr7:100487090-100487099 chr7:100487091-100487101
49	MXI1	chr7:100486897-100488256	H1-hESC	embryonic stem cell:	n/a	chr7:100487091-100487100
50	PBX3	chr7:100486232-100488370	SK-N-SH	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100487514-100487564	HRPEpiC	eye:	n/a
2	chr7:100487514-100487564	GM06990	blood:	n/a
3	chr7:100487514-100487564	Caco-2	colon:	n/a
4	chr7:100487514-100487564	AG09319	gingival:	n/a
5	chr7:100487514-100487564	HL-60	blood:	n/a
6	chr7:100487514-100487564	GM19239	blood:	n/a
7	chr7:100487514-100487564	HEEpiC	esophagus:	n/a
8	chr7:100487514-100487564	SK-N-SH	brain:	n/a
9	chr7:100487514-100487564	PANC-1	pancreas:	n/a
10	chr7:100487514-100487564	SK-N-MC	brain:	n/a
11	chr7:100487514-100487564	ECC-1	luminal epithelium:	n/a
12	chr7:100487514-100487564	ProgFib	skin:	n/a
13	chr7:100487514-100487564	HCM	heart:	n/a
14	chr7:100487514-100487564	BE2_C	brain:	n/a
15	chr7:100487514-100487564	NB4	blood:	n/a
16	chr7:100487514-100487564	K562	blood:	n/a
17	chr7:100487514-100487564	HCT-116	colon:	n/a
18	chr7:100487514-100487564	NH-A	brain:	n/a
19	chr7:100487514-100487564	GM12891	blood:	n/a
20	chr7:100487514-100487564	SKMC	muscle:	n/a
21	chr7:100487514-100487564	Jurkat	blood:	n/a
22	chr7:100487514-100487564	Hela-S3	cervix:	n/a
23	chr7:100487514-100487564	HepG2	liver:	n/a
24	chr7:100487514-100487564	CMK	blood:	n/a
25	chr7:100487514-100487564	PrEC	prostate:	n/a
26	chr7:100487514-100487564	HAEpiC	amniotic membrane:	n/a
27	chr7:100487514-100487564	RPTEC	kidney:	n/a
28	chr7:100487514-100487564	BJ	skin:	n/a
29	chr7:100487514-100487564	NT2-D1	testis:	n/a
30	chr7:100487514-100487564	AoSMC	blood vessel:	n/a
31	chr7:100487514-100487564	GM12878	blood:	n/a
32	chr7:100487514-100487564	HUVEC	blood vessel:	n/a
33	chr7:100487514-100487564	MCF10A-Er-Src	breast:	n/a
34	chr7:100487514-100487564	HRE	kidney:	n/a
35	chr7:100487514-100487564	A549	lung:	n/a
36	chr7:100487514-100487564	H1-hESC	embryonic stem cell:	embryo
37	chr7:100487514-100487564	U87	brain:	n/a
38	chr7:100487514-100487564	AG04450	lung:	fetal
39	chr7:100487514-100487564	PFSK-1	brain:	n/a
40	chr7:100487514-100487564	IMR90	lung:	fetal
41	chr7:100487514-100487564	HEK293	kidney:	embryo
42	chr7:100487514-100487564	LNCaP	prostate:	n/a
43	chr7:100487514-100487564	AG10803	skin:	n/a
44	chr7:100487514-100487564	AG04449	skin:	fetal
45	chr7:100487514-100487564	MCF-7	breast:	n/a
46	chr7:100487514-100487564	GM12892	blood:	n/a
47	chr7:100487514-100487564	SAEC	small airway:	n/a
48	chr7:100487514-100487564	NHBE	bronchial:	n/a
49	chr7:100487514-100487564	NHDF-neo	bronchial:	n/a
50	chr7:100487514-100487564	HPAEpiC	pulmonary alveolar:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100486439..100489230-chr7:100726552..100729974,6	MCF-7	breast:
2	chr7:100418397..100419909-chr7:100486584..100488563,2	MCF-7	breast:
3	chr7:100303615..100305529-chr7:100486314..100489038,2	K562	blood:
4	chr7:100402719..100405578-chr7:100487091..100488628,2	K562	blood:
5	chr7:100485568..100489865-chr7:100727204..100729829,6	MCF-7	breast:
6	chr7:100486144..100489424-chr7:100805467..100808505,5	MCF-7	breast:
7	chr1:179712115..179713115-chr7:100486907..100487582,2	MCF-7	breast:
8	chr7:100024866..100028113-chr7:100485356..100489963,5	MCF-7	breast:
9	chr7:100269556..100272634-chr7:100485447..100488529,3	K562	blood:
10	chr7:100487486..100489308-chr7:100879476..100881483,2	K562	blood:
11	chr7:100269920..100272546-chr7:100486381..100488020,2	MCF-7	breast:
12	chr3:125093829..125095736-chr7:100486331..100489025,2	MCF-7	breast:
13	chr7:100485751..100487913-chr7:100611034..100613104,2	K562	blood:
14	chr7:100486731..100489034-chr7:100894336..100897176,2	MCF-7	breast:
15	chr7:100486155..100488924-chr7:100732323..100735470,4	MCF-7	breast:
16	chr7:100486624..100489424-chr7:100545614..100548228,2	MCF-7	breast:
17	chr6:42749094..42751752-chr7:100485925..100488500,3	MCF-7	breast:
18	chr10:27149423..27150047-chr7:100487107..100487691,2	Hela-S3	cervix:
19	chr7:100447367..100452420-chr7:100484839..100489079,9	MCF-7	breast:
20	chr6:24774752..24775406-chr7:100486913..100487602,2	HCT-116	colon:
21	chr7:100486587..100489014-chr7:100735698..100737931,3	MCF-7	breast:
22	chr7:100433653..100435265-chr7:100487454..100490757,3	MCF-7	breast:
23	chr7:100182211..100184849-chr7:100486903..100489190,3	MCF-7	breast:
24	chr7:100487290..100489665-chr7:100607825..100610804,2	K562	blood:
25	chr7:100485984..100488072-chr7:100806477..100808899,2	K562	blood:
26	chr15:60689899..60690503-chr7:100486937..100487820,2	Hela-S3	cervix:
27	chr13:31736451..31736972-chr7:100487069..100487988,2	HCT-116	colon:
28	chr7:100448922..100451627-chr7:100483976..100487908,4	K562	blood:
29	chr7:63773941..63774744-chr7:100487108..100487984,2	NB4	blood:
30	chr7:100486719..100488706-chr7:100796879..100799403,2	MCF-7	breast:
31	chr7:100299982..100306646-chr7:100485585..100490991,8	MCF-7	breast:
32	chr7:100201842..100204261-chr7:100485824..100488204,2	MCF-7	breast:
33	chr7:100208465..100211590-chr7:100485559..100488810,4	MCF-7	breast:
34	chr7:100486477..100489401-chr7:100859928..100862607,2	MCF-7	breast:
35	chr7:100486764..100489719-chr7:100736778..100738797,2	K562	blood:
36	chr7:100487416..100489348-chr7:101516491..101519278,2	MCF-7	breast:
37	chr7:100484134..100489082-chr7:100804986..100809404,8	MCF-7	breast:
38	chr7:100486083..100488238-chr7:100659648..100662388,2	MCF-7	breast:
39	chr7:100472344..100473067-chr7:100487033..100488215,3	MCF-7	breast:
40	chr7:100423550..100425060-chr7:100485976..100488045,2	K562	blood:
41	chr7:100423424..100426106-chr7:100484562..100490364,9	MCF-7	breast:

No data

Variant related genes	Relation type
UFSP1	TF binding region
UFSP1	CpG island
ENSG00000225946	Chromatin interaction
ENSG00000112624	Chromatin interaction
ENSG00000205277	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000236305	Chromatin interaction
ENSG00000263672	Chromatin interaction
ENSG00000228273	Chromatin interaction
ENSG00000136754	Chromatin interaction
ENSG00000234444	Chromatin interaction
ENSG00000106333	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000227053	Chromatin interaction
ENSG00000112312	Chromatin interaction
ENSG00000128564	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000106330	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000087087	Chromatin interaction
ENSG00000182718	Chromatin interaction
ENSG00000120694	Chromatin interaction
ENSG00000169894	Chromatin interaction
ENSG00000214253	Chromatin interaction
ENSG00000172354	Chromatin interaction
ENSG00000106400	Chromatin interaction
ENSG00000260336	Chromatin interaction
ENSG00000106367	Chromatin interaction
ENSG00000196411	Chromatin interaction
ENSG00000106404	Chromatin interaction
ENSG00000169871	Chromatin interaction
ENSG00000172336	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000163848	Chromatin interaction
ENSG00000143340	Chromatin interaction
ENSG00000106397	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10278546	0.86[ASN][1000 genomes]
rs34803625	1.00[CHD][hapmap]
rs55754661	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56181548	0.81[AMR][1000 genomes]
rs57708886	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs59441762	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs66775024	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][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	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active 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	90 gene(s)	inside rSNPs	diseases
7	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
9	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
10	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
12	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer 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	90 gene(s)	inside rSNPs	diseases
13	nsv831073	chr7:100425659-100544888	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
14	nsv888802	chr7:100484917-100495530	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
15	nsv607967	chr7:100486016-100487748	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	37 gene(s)	inside rSNPs	diseases
16	nsv607968	chr7:100486035-100492896	Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	39 gene(s)	inside rSNPs	diseases
17	nsv888803	chr7:100486656-100497131	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
18	nsv888804	chr7:100486754-100494202	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
19	nsv888805	chr7:100486754-100498057	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 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	chr7:100484800-100488800	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr7:100486000-100488400	Active TSS	Psoas Muscle	Psoas
3	chr7:100486200-100489000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:100486400-100488400	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr7:100486400-100489200	Active TSS	H9 Cell Line	embryonic stem cell
6	chr7:100486400-100489400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:100486600-100487600	Active TSS	Hela-S3	cervix
8	chr7:100486600-100487800	Active TSS	H1 Cell Line	embryonic stem cell
9	chr7:100486600-100487800	Active TSS	Fetal Brain Female	brain
10	chr7:100486600-100487800	Active TSS	GM12878-XiMat	blood
11	chr7:100486600-100487800	Active TSS	HSMMtube	muscle
12	chr7:100486600-100488000	Active TSS	NHEK	skin
13	chr7:100486600-100488600	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr7:100486600-100488600	Active TSS	Placenta Amnion	Placenta Amnion
15	chr7:100486600-100489000	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr7:100486600-100489000	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr7:100486600-100489000	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr7:100486600-100489000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:100486600-100489000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:100486600-100489000	Active TSS	Rectal Smooth Muscle	rectum
21	chr7:100486600-100489200	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr7:100486600-100489200	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr7:100486600-100489200	Active TSS	Fetal Kidney	kidney
24	chr7:100486600-100489400	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr7:100486600-100489400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr7:100486600-100489400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:100486600-100489400	Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr7:100486600-100490600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:100486800-100487600	Active TSS	Brain Germinal Matrix	brain
30	chr7:100486800-100487600	Weak transcription	Fetal Heart	heart
31	chr7:100486800-100487600	Active TSS	Fetal Intestine Large	intestine
32	chr7:100486800-100487600	Active TSS	Osteobl	bone
33	chr7:100486800-100487800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:100486800-100487800	Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr7:100486800-100487800	Active TSS	Muscle Satellite Cultured Cells	--
36	chr7:100486800-100487800	Active TSS	Brain Angular Gyrus	brain
37	chr7:100486800-100487800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr7:100486800-100487800	Active TSS	Duodenum Mucosa	Duodenum
39	chr7:100486800-100487800	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr7:100486800-100487800	Active TSS	HSMM	muscle
41	chr7:100486800-100488000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:100486800-100488000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr7:100486800-100488000	Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr7:100486800-100488000	Active TSS	Brain Cingulate Gyrus	brain
45	chr7:100486800-100488000	Active TSS	Esophagus	oesophagus
46	chr7:100486800-100488000	Active TSS	Small Intestine	intestine
47	chr7:100486800-100488200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:100486800-100488200	Active TSS	Aorta	Aorta
49	chr7:100486800-100488200	Active TSS	Left Ventricle	heart
50	chr7:100486800-100488200	Active TSS	NHDF-Ad	bronchial

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