Variant report

Variant	nsv1034662
Chromosome Location	chr7:70275712-70722953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1653)
CpG islands
(count:2626)
Chromatin interactive
region (count:35)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1653 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70295432-70295731	HepG2	liver:	n/a	n/a
2	ATF1	chr7:70473461-70473667	K562	blood:	n/a	n/a
3	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
6	ATF2	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:70321901-70322317	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:70359196-70359849	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:70596126-70596870	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:70384908-70384986	K562	blood:	n/a	n/a
12	BACH1	chr7:70277553-70277731	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr7:70578379-70578450	K562	blood:	n/a	n/a
16	BACH1	chr7:70597821-70597985	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr7:70294291-70294547	GM12878	blood:	n/a	n/a
18	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:70359245-70359587	H1-hESC	embryonic stem cell:	n/a	n/a
20	BHLHE40	chr7:70294189-70294529	K562	blood:	n/a	n/a
21	BHLHE40	chr7:70685554-70685594	K562	blood:	n/a	n/a
22	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
23	BHLHE40	chr7:70498977-70499038	K562	blood:	n/a	n/a
24	BHLHE40	chr7:70294194-70294616	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
26	BHLHE40	chr7:70470205-70470386	K562	blood:	n/a	n/a
27	BHLHE40	chr7:70295491-70295711	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:70664067-70664139	K562	blood:	n/a	n/a
29	BHLHE40	chr7:70482560-70482896	K562	blood:	n/a	n/a
30	BRCA1	chr7:70294156-70294507	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr7:70277589-70277745	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr7:70515518-70515757	K562	blood:	n/a	n/a
33	CBX3	chr7:70538895-70539134	K562	blood:	n/a	n/a
34	CBX3	chr7:70482488-70483015	K562	blood:	n/a	n/a
35	CCNT2	chr7:70543176-70543345	K562	blood:	n/a	n/a
36	CEBPB	chr7:70294654-70294840	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:70692135-70692374	Hela-S3	cervix:	n/a	chr7:70692300-70692311
38	CEBPB	chr7:70295428-70295714	HepG2	liver:	n/a	chr7:70295552-70295563
39	CEBPB	chr7:70426416-70426613	K562	blood:	n/a	n/a
40	CEBPB	chr7:70614795-70614929	HepG2	liver:	n/a	chr7:70614859-70614872 chr7:70614860-70614871 chr7:70614859-70614870
41	CEBPB	chr7:70701507-70701812	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:70518584-70518708	A549	lung:	n/a	n/a
43	CEBPB	chr7:70686774-70686792	A549	lung:	n/a	n/a
44	CEBPB	chr7:70686647-70686901	HepG2	liver:	n/a	chr7:70686741-70686752
45	CEBPB	chr7:70299455-70299763	K562	blood:	n/a	chr7:70299603-70299614
46	CEBPB	chr7:70520571-70520875	Hela-S3	cervix:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
47	CEBPB	chr7:70520567-70520872	H1-hESC	embryonic stem cell:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
48	CEBPB	chr7:70635081-70635277	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:70696900-70697215	MCF-7	breast:	n/a	n/a
50	CEBPB	chr7:70520613-70520780	K562	blood:	n/a	chr7:70520680-70520691 chr7:70520691-70520702

(count:2626 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70599643-70599693	T-47D	breast:	n/a
2	chr7:70482771-70482821	A549	lung:	n/a
3	chr7:70597065-70597115	ProgFib	skin:	n/a
4	chr7:70599643-70599693	T-47D	breast:	n/a
5	chr7:70482771-70482821	A549	lung:	n/a
6	chr7:70597065-70597115	ProgFib	skin:	n/a
7	chr7:70597599-70597649	HEK293	kidney:	embryo
8	chr7:70577170-70577220	HL-60	blood:	n/a
9	chr7:70598282-70598332	H1-hESC	embryonic stem cell:	embryo
10	chr7:70630583-70630633	U87	brain:	n/a
11	chr7:70543320-70543370	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:70666259-70666309	HMEC	breast:	n/a
13	chr7:70596308-70596358	Jurkat	blood:	n/a
14	chr7:70561125-70561175	HRPEpiC	eye:	n/a
15	chr7:70702212-70702262	HUVEC	blood vessel:	n/a
16	chr7:70294525-70294575	T-47D	breast:	n/a
17	chr7:70543079-70543129	K562	blood:	n/a
18	chr7:70543079-70543129	PFSK-1	brain:	n/a
19	chr7:70630583-70630633	AG04450	lung:	fetal
20	chr7:70322401-70322451	SK-N-MC	brain:	n/a
21	chr7:70596377-70596427	GM06990	blood:	n/a
22	chr7:70595507-70595557	Hepatocyte	liver:	n/a
23	chr7:70543079-70543129	HEEpiC	esophagus:	n/a
24	chr7:70597687-70597737	AG10803	skin:	n/a
25	chr7:70597599-70597649	PFSK-1	brain:	n/a
26	chr7:70597774-70597824	AG09309	skin:	n/a
27	chr7:70294525-70294575	HEEpiC	esophagus:	n/a
28	chr7:70599516-70599566	GM12891	blood:	n/a
29	chr7:70592898-70592948	AoSMC	blood vessel:	n/a
30	chr7:70597687-70597737	SK-N-SH	brain:	n/a
31	chr7:70601102-70601152	U87	brain:	n/a
32	chr7:70597778-70597828	AG10803	skin:	n/a
33	chr7:70543800-70543850	LNCaP	prostate:	n/a
34	chr7:70322401-70322451	HEK293	kidney:	embryo
35	chr7:70666259-70666309	PANC-1	pancreas:	n/a
36	chr7:70597687-70597737	HL-60	blood:	n/a
37	chr7:70543320-70543370	AG04450	lung:	fetal
38	chr7:70596377-70596427	NHDF-neo	bronchial:	n/a
39	chr7:70599516-70599566	A549	lung:	n/a
40	chr7:70482891-70482941	Jurkat	blood:	n/a
41	chr7:70597687-70597737	H1-hESC	embryonic stem cell:	embryo
42	chr7:70322401-70322451	AG09309	skin:	n/a
43	chr7:70597065-70597115	HepG2	liver:	n/a
44	chr7:70322401-70322451	GM12891	blood:	n/a
45	chr7:70311321-70311371	NB4	blood:	n/a
46	chr7:70597687-70597737	HEEpiC	esophagus:	n/a
47	chr7:70599643-70599693	RPTEC	kidney:	n/a
48	chr7:70311321-70311371	PrEC	prostate:	n/a
49	chr7:70596377-70596427	Caco-2	colon:	n/a
50	chr7:70359655-70359705	ovcar-3	ovarian:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
2	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
3	chr7:70293845..70294790-chr7:71197836..71198902,6	K562	blood:
4	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
5	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
6	chr7:70574285..70576318-chr7:70581134..70583277,2	K562	blood:
7	chr7:70294117..70295302-chr7:71197788..71199575,6	MCF-7	breast:
8	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
9	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
10	chr7:70700080..70701840-chr7:70703874..70706037,2	MCF-7	breast:
11	chr7:70700080..70701840-chr7:70703874..70706037,2	MCF-7	breast:
12	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
13	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
14	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
15	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
16	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
17	chr7:70472764..70475068-chr7:70478258..70480877,2	K562	blood:
18	chr7:70295507..70296249-chr7:71198004..71198896,2	MCF-7	breast:
19	chr7:70574285..70576318-chr7:70581134..70583277,2	K562	blood:
20	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
21	chr7:70294183..70294797-chr7:71197949..71198693,3	MCF-7	breast:
22	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
23	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
24	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
25	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
26	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
27	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
28	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
29	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
30	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
31	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
32	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
33	chr7:70472764..70475068-chr7:70478258..70480877,2	K562	blood:
34	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
35	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AUTS2-3	chr7:70302724-70302999	NONHSAT121342

No data

Variant related genes	Relation type
WBSCR17	TF binding region
ENSG00000236978	TF binding region
WBSCR17	CpG island
ENSG00000236978	CpG island

Extended variants
information (count: 14589 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:14589 , 50 per page) page: 1 2 3 4 5 6 7 ... 292

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564193778	chr7:70275713-70275714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs60106397	chr7:70275739-70275740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528386394	chr7:70275759-70275760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546436120	chr7:70275783-70275784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191302472	chr7:70275820-70275821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535952218	chr7:70275838-70275839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548601378	chr7:70275842-70275843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551125556	chr7:70275956-70275957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569262631	chr7:70275973-70275974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs6460560	chr7:70275976-70275977	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs368160049	chr7:70276020-70276021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371918652	chr7:70276043-70276044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573412252	chr7:70276053-70276054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534518719	chr7:70276055-70276056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540102839	chr7:70276067-70276068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555533037	chr7:70276078-70276079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182889324	chr7:70276108-70276109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541506842	chr7:70276117-70276118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563010854	chr7:70276187-70276188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6460561	chr7:70276247-70276248	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs149377680	chr7:70276251-70276252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564116029	chr7:70276276-70276277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570130143	chr7:70276300-70276301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528362909	chr7:70276328-70276329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540582600	chr7:70276334-70276335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527396162	chr7:70276359-70276360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144711058	chr7:70276362-70276363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372485305	chr7:70276384-70276385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529138573	chr7:70276410-70276411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550813439	chr7:70276428-70276429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569225375	chr7:70276429-70276430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547147653	chr7:70276431-70276432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533470142	chr7:70276508-70276509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551447508	chr7:70276530-70276531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566898914	chr7:70276638-70276639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187225806	chr7:70276650-70276651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191044013	chr7:70276659-70276660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6972818	chr7:70276691-70276692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187978210	chr7:70276713-70276714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567330185	chr7:70276721-70276722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192252342	chr7:70276722-70276723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182706584	chr7:70276742-70276743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555727890	chr7:70276767-70276768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570020319	chr7:70276773-70276774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572826752	chr7:70276783-70276784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540519508	chr7:70276787-70276788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561932864	chr7:70276818-70276819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529229246	chr7:70276843-70276844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544375589	chr7:70276902-70276903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371097442	chr7:70276907-70276908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1900 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70274200-70276600	Enhancers	Liver	Liver
2	chr7:70274600-70275800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr7:70275800-70276000	Enhancers	Primary B cells from peripheral blood	blood
4	chr7:70276600-70277000	Weak transcription	Liver	Liver
5	chr7:70277000-70279000	Enhancers	Liver	Liver
6	chr7:70277400-70277800	Enhancers	Fetal Intestine Large	intestine
7	chr7:70277400-70277800	Enhancers	Fetal Intestine Small	intestine
8	chr7:70281400-70281600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr7:70281600-70286600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:70285800-70287200	Enhancers	Liver	Liver
11	chr7:70286600-70286800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr7:70291600-70294400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:70294000-70294200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr7:70294000-70294200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:70294000-70294200	Enhancers	Dnd41	blood
16	chr7:70294000-70294400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr7:70294000-70294400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:70294000-70294400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr7:70294000-70294400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr7:70294000-70294400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:70294000-70294400	Enhancers	Brain Angular Gyrus	brain
22	chr7:70294000-70294400	Active TSS	Brain Anterior Caudate	brain
23	chr7:70294000-70294400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
24	chr7:70294000-70294400	Enhancers	Fetal Brain Male	brain
25	chr7:70294000-70294400	Enhancers	Fetal Muscle Trunk	muscle
26	chr7:70294000-70294400	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr7:70294000-70294400	Bivalent Enhancer	Fetal Stomach	stomach
28	chr7:70294000-70294400	Enhancers	GM12878-XiMat	blood
29	chr7:70294000-70294400	Enhancers	HSMM	muscle
30	chr7:70294000-70294600	Enhancers	HMEC	breast
31	chr7:70294000-70294800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr7:70294000-70295200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
33	chr7:70294000-70296400	Enhancers	Liver	Liver
34	chr7:70294200-70294400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr7:70294200-70294400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:70294200-70294400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:70294200-70294400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr7:70294200-70294400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:70294200-70294400	Enhancers	Primary hematopoietic stem cells	blood
40	chr7:70294200-70294400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr7:70294200-70294400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr7:70294200-70294400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:70294200-70294400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:70294200-70294400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr7:70294200-70294400	Active TSS	Brain Hippocampus Middle	brain
46	chr7:70294200-70294400	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr7:70294200-70294400	Enhancers	Brain Substantia Nigra	brain
48	chr7:70294200-70294400	Enhancers	Fetal Brain Female	brain
49	chr7:70294200-70294400	Enhancers	Ovary	ovary
50	chr7:70294200-70294400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle

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