Variant report

Variant	esv3350369
Chromosome Location	chr7:70288094-70503884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1061)
CpG islands
(count:671)
Chromatin interactive
region (count:30)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:70359196-70359849	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70314522-70315080	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	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
9	ATF2	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:70384908-70384986	K562	blood:	n/a	n/a
11	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:70294291-70294547	GM12878	blood:	n/a	n/a
14	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:70359245-70359587	H1-hESC	embryonic stem cell:	n/a	n/a
16	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
17	BHLHE40	chr7:70294189-70294529	K562	blood:	n/a	n/a
18	BHLHE40	chr7:70295491-70295711	HepG2	liver:	n/a	n/a
19	BHLHE40	chr7:70482560-70482896	K562	blood:	n/a	n/a
20	BHLHE40	chr7:70498977-70499038	K562	blood:	n/a	n/a
21	BHLHE40	chr7:70470205-70470386	K562	blood:	n/a	n/a
22	BHLHE40	chr7:70294194-70294616	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
24	BRCA1	chr7:70294156-70294507	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr7:70482488-70483015	K562	blood:	n/a	n/a
26	CEBPB	chr7:70349310-70349766	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:70473685-70474059	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:70477784-70478010	H1-hESC	embryonic stem cell:	n/a	chr7:70477953-70477964
29	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
30	CEBPB	chr7:70359237-70359569	H1-hESC	embryonic stem cell:	n/a	chr7:70359363-70359375
31	CEBPB	chr7:70473679-70474025	MCF-7	breast:	n/a	n/a
32	CEBPB	chr7:70477839-70478111	IMR90	lung:	n/a	chr7:70477953-70477964
33	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
34	CEBPB	chr7:70295315-70295710	HepG2	liver:	n/a	chr7:70295552-70295563
35	CEBPB	chr7:70477923-70478050	HepG2	liver:	n/a	chr7:70477953-70477964
36	CEBPB	chr7:70473715-70474044	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:70294172-70294801	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:70299440-70299798	HepG2	liver:	n/a	chr7:70299603-70299614
40	CEBPB	chr7:70295428-70295714	HepG2	liver:	n/a	chr7:70295552-70295563
41	CEBPB	chr7:70299422-70299775	IMR90	lung:	n/a	chr7:70299603-70299614
42	CEBPB	chr7:70491206-70491381	K562	blood:	n/a	chr7:70491297-70491308
43	CEBPB	chr7:70491156-70491389	HepG2	liver:	n/a	chr7:70491297-70491308
44	CEBPB	chr7:70409678-70409872	HepG2	liver:	n/a	chr7:70409738-70409749
45	CEBPB	chr7:70299453-70299778	A549	lung:	n/a	chr7:70299603-70299614
46	CEBPB	chr7:70426416-70426613	K562	blood:	n/a	n/a
47	CEBPB	chr7:70473682-70474054	K562	blood:	n/a	n/a
48	CEBPB	chr7:70426400-70426506	A549	lung:	n/a	n/a
49	CEBPB	chr7:70443503-70443748	HepG2	liver:	n/a	chr7:70443649-70443660 chr7:70443597-70443608
50	CEBPB	chr7:70299521-70299730	H1-hESC	embryonic stem cell:	n/a	chr7:70299603-70299614

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70322401-70322451	LNCaP	prostate:	n/a
2	chr7:70294264-70294314	NHBE	bronchial:	n/a
3	chr7:70359655-70359705	AG10803	skin:	n/a
4	chr7:70294264-70294314	GM19239	blood:	n/a
5	chr7:70294525-70294575	HRCEpiC	kidney:	n/a
6	chr7:70417419-70417469	PFSK-1	brain:	n/a
7	chr7:70311321-70311371	PFSK-1	brain:	n/a
8	chr7:70294264-70294314	HEEpiC	esophagus:	n/a
9	chr7:70311435-70311485	Hepatocyte	liver:	n/a
10	chr7:70311435-70311485	T-47D	breast:	n/a
11	chr7:70417419-70417469	BE2_C	brain:	n/a
12	chr7:70482771-70482821	AG04449	skin:	fetal
13	chr7:70294511-70294561	SAEC	small airway:	n/a
14	chr7:70311532-70311582	CMK	blood:	n/a
15	chr7:70311435-70311485	HEEpiC	esophagus:	n/a
16	chr7:70294264-70294314	BJ	skin:	n/a
17	chr7:70417419-70417469	NT2-D1	testis:	n/a
18	chr7:70294511-70294561	HEEpiC	esophagus:	n/a
19	chr7:70482771-70482821	T-47D	breast:	n/a
20	chr7:70482771-70482821	CMK	blood:	n/a
21	chr7:70311321-70311371	K562	blood:	n/a
22	chr7:70294264-70294314	ECC-1	luminal epithelium:	n/a
23	chr7:70322401-70322451	Caco-2	colon:	n/a
24	chr7:70359655-70359705	ProgFib	skin:	n/a
25	chr7:70482771-70482821	AG09319	gingival:	n/a
26	chr7:70311321-70311371	NT2-D1	testis:	n/a
27	chr7:70322401-70322451	GM12892	blood:	n/a
28	chr7:70294511-70294561	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:70294264-70294314	HepG2	liver:	n/a
30	chr7:70359655-70359705	PrEC	prostate:	n/a
31	chr7:70417419-70417469	HRPEpiC	eye:	n/a
32	chr7:70482891-70482941	NH-A	brain:	n/a
33	chr7:70322401-70322451	GM12878	blood:	n/a
34	chr7:70359655-70359705	NHBE	bronchial:	n/a
35	chr7:70482771-70482821	HEK293	kidney:	embryo
36	chr7:70482771-70482821	Hela-S3	cervix:	n/a
37	chr7:70322401-70322451	AG10803	skin:	n/a
38	chr7:70417419-70417469	T-47D	breast:	n/a
39	chr7:70294525-70294575	SKMC	muscle:	n/a
40	chr7:70311532-70311582	PrEC	prostate:	n/a
41	chr7:70322401-70322451	SK-N-SH_RA	brain:	n/a
42	chr7:70482771-70482821	HL-60	blood:	n/a
43	chr7:70294525-70294575	GM19239	blood:	n/a
44	chr7:70311321-70311371	Jurkat	blood:	n/a
45	chr7:70311321-70311371	HCF	heart:	n/a
46	chr7:70311321-70311371	BE2_C	brain:	n/a
47	chr7:70322401-70322451	BJ	skin:	n/a
48	chr7:70311321-70311371	LNCaP	prostate:	n/a
49	chr7:70294264-70294314	HCPEpiC	choroid plexus:	n/a
50	chr7:70311532-70311582	SKMC	muscle:	n/a

(count:30 , 50 per page) page: 1

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

(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
ENSG00000236978	TF binding region
ENSG00000236978	CpG island

Extended variants
information (count: 7019 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:7019 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185141466	chr7:70291610-70291611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374135212	chr7:70291611-70291612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555517781	chr7:70291658-70291659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190398688	chr7:70291678-70291679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544413663	chr7:70291708-70291709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533637448	chr7:70291727-70291728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145583090	chr7:70291743-70291744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577721351	chr7:70291755-70291756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544989992	chr7:70291760-70291761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560158267	chr7:70291766-70291767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183257918	chr7:70291790-70291791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111751287	chr7:70291804-70291805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561641507	chr7:70291816-70291817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531783416	chr7:70291859-70291860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138151903	chr7:70291864-70291865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568932173	chr7:70291921-70291922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377593845	chr7:70291930-70291931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200030509	chr7:70291953-70291954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577279877	chr7:70292013-70292014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576711132	chr7:70292082-70292083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201620650	chr7:70292097-70292098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533102067	chr7:70292129-70292130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373683100	chr7:70292140-70292141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551394136	chr7:70292200-70292201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375894760	chr7:70292222-70292223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188483569	chr7:70292231-70292232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200849947	chr7:70292243-70292244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369325111	chr7:70292268-70292269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543759389	chr7:70292286-70292287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372488957	chr7:70292291-70292292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544212562	chr7:70292294-70292295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11973930	chr7:70292316-70292317	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370949650	chr7:70292318-70292319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537606456	chr7:70292347-70292348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375808314	chr7:70292349-70292350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78929500	chr7:70292485-70292486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113857654	chr7:70292499-70292500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12667874	chr7:70292509-70292510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71077686	chr7:70292512-70292513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4718999	chr7:70292513-70292514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28842803	chr7:70292517-70292518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs55956176	chr7:70292522-70292523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28817091	chr7:70292523-70292524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs56236322	chr7:70292527-70292528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148235322	chr7:70292530-70292531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs55801547	chr7:70292531-70292532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149241374	chr7:70292533-70292534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28857290	chr7:70292535-70292536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527406380	chr7:70292541-70292542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191770847	chr7:70292548-70292549	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:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70291600-70294400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:70294000-70294200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr7:70294000-70294200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr7:70294000-70294200	Enhancers	Dnd41	blood
5	chr7:70294000-70294400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr7:70294000-70294400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:70294000-70294400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr7:70294000-70294400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr7:70294000-70294400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr7:70294000-70294400	Enhancers	Brain Angular Gyrus	brain
11	chr7:70294000-70294400	Active TSS	Brain Anterior Caudate	brain
12	chr7:70294000-70294400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
13	chr7:70294000-70294400	Enhancers	Fetal Brain Male	brain
14	chr7:70294000-70294400	Enhancers	Fetal Muscle Trunk	muscle
15	chr7:70294000-70294400	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr7:70294000-70294400	Bivalent Enhancer	Fetal Stomach	stomach
17	chr7:70294000-70294400	Enhancers	GM12878-XiMat	blood
18	chr7:70294000-70294400	Enhancers	HSMM	muscle
19	chr7:70294000-70294600	Enhancers	HMEC	breast
20	chr7:70294000-70294800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:70294000-70295200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:70294000-70296400	Enhancers	Liver	Liver
23	chr7:70294200-70294400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr7:70294200-70294400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:70294200-70294400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:70294200-70294400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:70294200-70294400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:70294200-70294400	Enhancers	Primary hematopoietic stem cells	blood
29	chr7:70294200-70294400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr7:70294200-70294400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr7:70294200-70294400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:70294200-70294400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:70294200-70294400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr7:70294200-70294400	Active TSS	Brain Hippocampus Middle	brain
35	chr7:70294200-70294400	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr7:70294200-70294400	Enhancers	Brain Substantia Nigra	brain
37	chr7:70294200-70294400	Enhancers	Fetal Brain Female	brain
38	chr7:70294200-70294400	Enhancers	Ovary	ovary
39	chr7:70294200-70294400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
40	chr7:70294200-70294400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
41	chr7:70294200-70294400	Flanking Active TSS	Dnd41	blood
42	chr7:70294200-70294400	Enhancers	NH-A	brain
43	chr7:70294200-70294600	Flanking Active TSS	Primary T cells from cord blood	blood
44	chr7:70294200-70294600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr7:70294200-70294600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:70294200-70295000	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr7:70294200-70295000	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr7:70294200-70295000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:70294400-70294600	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr7:70294400-70294600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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