Variant report

Variant	nsv429773
Chromosome Location	chr7:70285994-70357061
allele	n/a
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	ARID3A	chr7:70295432-70295731	HepG2	liver:	n/a	n/a
2	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70321901-70322317	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	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
7	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
11	BATF	chr7:70294291-70294547	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:70294189-70294529	K562	blood:	n/a	n/a
13	BHLHE40	chr7:70294194-70294616	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:70295491-70295711	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
16	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
17	BRCA1	chr7:70294156-70294507	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:70294172-70294801	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:70299455-70299763	K562	blood:	n/a	chr7:70299603-70299614
20	CEBPB	chr7:70349310-70349766	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
22	CEBPB	chr7:70299521-70299730	H1-hESC	embryonic stem cell:	n/a	chr7:70299603-70299614
23	CEBPB	chr7:70299453-70299778	A549	lung:	n/a	chr7:70299603-70299614
24	CEBPB	chr7:70294654-70294840	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:70295315-70295710	HepG2	liver:	n/a	chr7:70295552-70295563
26	CEBPB	chr7:70314283-70314959	H1-hESC	embryonic stem cell:	n/a	chr7:70314674-70314686
27	CEBPB	chr7:70299422-70299775	IMR90	lung:	n/a	chr7:70299603-70299614
28	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:70299440-70299798	HepG2	liver:	n/a	chr7:70299603-70299614
30	CEBPB	chr7:70295428-70295714	HepG2	liver:	n/a	chr7:70295552-70295563
31	CEBPB	chr7:70295452-70295643	HepG2	liver:	n/a	chr7:70295552-70295563
32	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
33	CEBPD	chr7:70295350-70295592	HepG2	liver:	n/a	n/a
34	CHD2	chr7:70294154-70294772	H1-hESC	embryonic stem cell:	n/a	chr7:70294263-70294270
35	CHD2	chr7:70323263-70323459	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr7:70314201-70315062	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr7:70294198-70294398	K562	blood:	n/a	chr7:70294263-70294270
38	CHD2	chr7:70294218-70294410	HepG2	liver:	n/a	chr7:70294263-70294270
39	CTBP2	chr7:70349262-70350113	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:70322000-70322150	HVMF	connective:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
41	CTCF	chr7:70322060-70322210	HVMF	connective:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
42	CTCF	chr7:70321986-70322220	NHEK	skin:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
43	CTCF	chr7:70321984-70322213	HepG2	liver:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
44	CTCF	chr7:70321763-70321838	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr7:70294220-70294370	GM12868	blood:	n/a	chr7:70294310-70294326 chr7:70294311-70294332 chr7:70294309-70294327
46	CTCF	chr7:70294217-70294485	A549	lung:	n/a	chr7:70294310-70294326 chr7:70294311-70294332 chr7:70294309-70294327
47	CTCF	chr7:70322020-70322170	GM12878	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
48	CTCF	chr7:70322040-70322190	GM12873	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
49	CTCF	chr7:70321700-70321850	GM12868	blood:	n/a	n/a
50	CTCF	chr7:70321980-70322206	MCF-7	breast:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70311532-70311582	PFSK-1	brain:	n/a
2	chr7:70294525-70294575	HepG2	liver:	n/a
3	chr7:70311532-70311582	PFSK-1	brain:	n/a
4	chr7:70294525-70294575	HepG2	liver:	n/a
5	chr7:70311321-70311371	HCPEpiC	choroid plexus:	n/a
6	chr7:70322401-70322451	HMEC	breast:	n/a
7	chr7:70294511-70294561	HRCEpiC	kidney:	n/a
8	chr7:70311321-70311371	GM12891	blood:	n/a
9	chr7:70294264-70294314	PFSK-1	brain:	n/a
10	chr7:70294525-70294575	CMK	blood:	n/a
11	chr7:70311321-70311371	HRE	kidney:	n/a
12	chr7:70311321-70311371	Hela-S3	cervix:	n/a
13	chr7:70294264-70294314	HepG2	liver:	n/a
14	chr7:70294511-70294561	HUVEC	blood vessel:	n/a
15	chr7:70294264-70294314	HIPEpiC	eye:	n/a
16	chr7:70311532-70311582	ProgFib	skin:	n/a
17	chr7:70311532-70311582	HEK293	kidney:	embryo
18	chr7:70322401-70322451	HCPEpiC	choroid plexus:	n/a
19	chr7:70294511-70294561	HEEpiC	esophagus:	n/a
20	chr7:70294264-70294314	GM19239	blood:	n/a
21	chr7:70294525-70294575	U87	brain:	n/a
22	chr7:70311321-70311371	SKMC	muscle:	n/a
23	chr7:70311532-70311582	K562	blood:	n/a
24	chr7:70322401-70322451	HCT-116	colon:	n/a
25	chr7:70322401-70322451	HepG2	liver:	n/a
26	chr7:70311321-70311371	SAEC	small airway:	n/a
27	chr7:70294511-70294561	GM12892	blood:	n/a
28	chr7:70311532-70311582	HepG2	liver:	n/a
29	chr7:70322401-70322451	Caco-2	colon:	n/a
30	chr7:70294264-70294314	H1-hESC	embryonic stem cell:	embryo
31	chr7:70322401-70322451	BE2_C	brain:	n/a
32	chr7:70311435-70311485	GM12891	blood:	n/a
33	chr7:70311435-70311485	Hela-S3	cervix:	n/a
34	chr7:70322401-70322451	NB4	blood:	n/a
35	chr7:70311321-70311371	HCM	heart:	n/a
36	chr7:70294525-70294575	H1-hESC	embryonic stem cell:	embryo
37	chr7:70311435-70311485	HCM	heart:	n/a
38	chr7:70322401-70322451	K562	blood:	n/a
39	chr7:70294525-70294575	NT2-D1	testis:	n/a
40	chr7:70294511-70294561	BJ	skin:	n/a
41	chr7:70311435-70311485	HL-60	blood:	n/a
42	chr7:70294264-70294314	HMEC	breast:	n/a
43	chr7:70294264-70294314	K562	blood:	n/a
44	chr7:70311321-70311371	K562	blood:	n/a
45	chr7:70294511-70294561	HNPCEpiC	eye:	n/a
46	chr7:70322401-70322451	IMR90	lung:	fetal
47	chr7:70311435-70311485	SK-N-MC	brain:	n/a
48	chr7:70322401-70322451	BJ	skin:	n/a
49	chr7:70294525-70294575	GM12892	blood:	n/a
50	chr7:70294511-70294561	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:70294117..70295302-chr7:71197788..71199575,6	MCF-7	breast:
2	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
3	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
4	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
5	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
6	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
7	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
8	chr7:70294183..70294797-chr7:71197949..71198693,3	MCF-7	breast:
9	chr7:70295507..70296249-chr7:71198004..71198896,2	MCF-7	breast:
10	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
11	chr7:70293845..70294790-chr7:71197836..71198902,6	K562	blood:
12	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
13	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
14	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
15	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
16	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
17	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
18	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
19	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
20	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:

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

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

Extended variants
information (count: 2584 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2584 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11486733	chr7:70285994-70285995	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544816778	chr7:70286004-70286005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538567954	chr7:70286020-70286021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139824519	chr7:70286086-70286087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192104490	chr7:70286087-70286088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1949979	chr7:70286089-70286090	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs111670405	chr7:70286102-70286103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543788428	chr7:70286142-70286143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565462301	chr7:70286158-70286159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73170260	chr7:70286171-70286172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548032707	chr7:70286215-70286216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11983277	chr7:70286254-70286255	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs142075770	chr7:70286318-70286319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571001962	chr7:70286320-70286321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs151138404	chr7:70286352-70286353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371784077	chr7:70286407-70286408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140641153	chr7:70286408-70286409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538126380	chr7:70286435-70286436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556147611	chr7:70286483-70286484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571226669	chr7:70286494-70286495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538398455	chr7:70286495-70286496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553560459	chr7:70286558-70286559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141001346	chr7:70286586-70286587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs398111452	chr7:70286596-70286597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1997225	chr7:70286597-70286598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs184041531	chr7:70286657-70286658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186075478	chr7:70286658-70286659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150060480	chr7:70286661-70286662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147720785	chr7:70286662-70286663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114587468	chr7:70286683-70286684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376517059	chr7:70286712-70286713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566832673	chr7:70286716-70286717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532860228	chr7:70286742-70286743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554223697	chr7:70286747-70286748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113580930	chr7:70286766-70286767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527380311	chr7:70286768-70286769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371854276	chr7:70286807-70286808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375640072	chr7:70286840-70286841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550681973	chr7:70286958-70286959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535462972	chr7:70286989-70286990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561052087	chr7:70287001-70287002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs77053295	chr7:70287038-70287039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10259518	chr7:70287039-70287040	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs571167702	chr7:70287094-70287095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371835560	chr7:70287104-70287105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538587567	chr7:70287119-70287120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547185713	chr7:70287167-70287168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148949452	chr7:70287197-70287198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185141466	chr7:70291610-70291611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374135212	chr7:70291611-70291612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70281600-70286600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:70285800-70287200	Enhancers	Liver	Liver
3	chr7:70286600-70286800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:70291600-70294400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:70294000-70294200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr7:70294000-70294200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:70294000-70294200	Enhancers	Dnd41	blood
8	chr7:70294000-70294400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr7:70294000-70294400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:70294000-70294400	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr7:70294000-70294400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
12	chr7:70294000-70294400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr7:70294000-70294400	Enhancers	Brain Angular Gyrus	brain
14	chr7:70294000-70294400	Active TSS	Brain Anterior Caudate	brain
15	chr7:70294000-70294400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
16	chr7:70294000-70294400	Enhancers	Fetal Brain Male	brain
17	chr7:70294000-70294400	Enhancers	Fetal Muscle Trunk	muscle
18	chr7:70294000-70294400	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr7:70294000-70294400	Bivalent Enhancer	Fetal Stomach	stomach
20	chr7:70294000-70294400	Enhancers	GM12878-XiMat	blood
21	chr7:70294000-70294400	Enhancers	HSMM	muscle
22	chr7:70294000-70294600	Enhancers	HMEC	breast
23	chr7:70294000-70294800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:70294000-70295200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:70294000-70296400	Enhancers	Liver	Liver
26	chr7:70294200-70294400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr7:70294200-70294400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:70294200-70294400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:70294200-70294400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr7:70294200-70294400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:70294200-70294400	Enhancers	Primary hematopoietic stem cells	blood
32	chr7:70294200-70294400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr7:70294200-70294400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:70294200-70294400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:70294200-70294400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:70294200-70294400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:70294200-70294400	Active TSS	Brain Hippocampus Middle	brain
38	chr7:70294200-70294400	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr7:70294200-70294400	Enhancers	Brain Substantia Nigra	brain
40	chr7:70294200-70294400	Enhancers	Fetal Brain Female	brain
41	chr7:70294200-70294400	Enhancers	Ovary	ovary
42	chr7:70294200-70294400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
43	chr7:70294200-70294400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
44	chr7:70294200-70294400	Flanking Active TSS	Dnd41	blood
45	chr7:70294200-70294400	Enhancers	NH-A	brain
46	chr7:70294200-70294600	Flanking Active TSS	Primary T cells from cord blood	blood
47	chr7:70294200-70294600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr7:70294200-70294600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:70294200-70295000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr7:70294200-70295000	Enhancers	Primary T helper cells PMA-I stimulated	--

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