Variant report

Variant	nsv1031764
Chromosome Location	chr7:70271645-70420426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1135)
CpG islands
(count:551)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1135 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
5	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70359196-70359849	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	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:70277553-70277731	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:70384908-70384986	K562	blood:	n/a	n/a
13	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
14	BATF	chr7:70294291-70294547	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	chr7:70294194-70294616	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
21	BRCA1	chr7:70277589-70277745	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr7:70294156-70294507	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:70314283-70314959	H1-hESC	embryonic stem cell:	n/a	chr7:70314674-70314686
24	CEBPB	chr7:70275675-70275878	K562	blood:	n/a	chr7:70275762-70275779
25	CEBPB	chr7:70299455-70299763	K562	blood:	n/a	chr7:70299603-70299614
26	CEBPB	chr7:70359237-70359569	H1-hESC	embryonic stem cell:	n/a	chr7:70359363-70359375
27	CEBPB	chr7:70349310-70349766	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr7:70294654-70294840	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:70277650-70277842	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:70295428-70295714	HepG2	liver:	n/a	chr7:70295552-70295563
31	CEBPB	chr7:70299521-70299730	H1-hESC	embryonic stem cell:	n/a	chr7:70299603-70299614
32	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
34	CEBPB	chr7:70294172-70294801	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:70295452-70295643	HepG2	liver:	n/a	chr7:70295552-70295563
36	CEBPB	chr7:70299422-70299775	IMR90	lung:	n/a	chr7:70299603-70299614
37	CEBPB	chr7:70275646-70275979	HepG2	liver:	n/a	chr7:70275762-70275779
38	CEBPB	chr7:70295315-70295710	HepG2	liver:	n/a	chr7:70295552-70295563
39	CEBPB	chr7:70388372-70388507	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:70299440-70299798	HepG2	liver:	n/a	chr7:70299603-70299614
41	CEBPB	chr7:70275577-70275965	HepG2	liver:	n/a	chr7:70275762-70275779
42	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
43	CEBPB	chr7:70275639-70275877	A549	lung:	n/a	chr7:70275762-70275779
44	CEBPB	chr7:70409678-70409872	HepG2	liver:	n/a	chr7:70409738-70409749
45	CEBPB	chr7:70275643-70275871	HepG2	liver:	n/a	chr7:70275762-70275779
46	CEBPB	chr7:70299453-70299778	A549	lung:	n/a	chr7:70299603-70299614
47	CEBPD	chr7:70295350-70295592	HepG2	liver:	n/a	n/a
48	CHD1	chr7:70359526-70359680	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr7:70323263-70323459	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr7:70314201-70315062	H1-hESC	embryonic stem cell:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70294525-70294575	HAEpiC	amniotic membrane:	n/a
2	chr7:70322401-70322451	HCPEpiC	choroid plexus:	n/a
3	chr7:70294525-70294575	HAEpiC	amniotic membrane:	n/a
4	chr7:70322401-70322451	HCPEpiC	choroid plexus:	n/a
5	chr7:70311532-70311582	GM12892	blood:	n/a
6	chr7:70359655-70359705	GM12878	blood:	n/a
7	chr7:70311435-70311485	ECC-1	luminal epithelium:	n/a
8	chr7:70322401-70322451	SK-N-MC	brain:	n/a
9	chr7:70311321-70311371	HIPEpiC	eye:	n/a
10	chr7:70311435-70311485	HNPCEpiC	eye:	n/a
11	chr7:70294264-70294314	HCM	heart:	n/a
12	chr7:70359655-70359705	Hepatocyte	liver:	n/a
13	chr7:70322401-70322451	NT2-D1	testis:	n/a
14	chr7:70311321-70311371	AG09319	gingival:	n/a
15	chr7:70294525-70294575	MCF10A-Er-Src	breast:	n/a
16	chr7:70417419-70417469	ProgFib	skin:	n/a
17	chr7:70322401-70322451	HMEC	breast:	n/a
18	chr7:70311532-70311582	PrEC	prostate:	n/a
19	chr7:70311532-70311582	GM12878	blood:	n/a
20	chr7:70311435-70311485	HMEC	breast:	n/a
21	chr7:70322401-70322451	NH-A	brain:	n/a
22	chr7:70294511-70294561	AoSMC	blood vessel:	n/a
23	chr7:70359655-70359705	NB4	blood:	n/a
24	chr7:70311321-70311371	SK-N-SH	brain:	n/a
25	chr7:70294511-70294561	ECC-1	luminal epithelium:	n/a
26	chr7:70294525-70294575	CMK	blood:	n/a
27	chr7:70322401-70322451	SAEC	small airway:	n/a
28	chr7:70417419-70417469	T-47D	breast:	n/a
29	chr7:70294525-70294575	HRCEpiC	kidney:	n/a
30	chr7:70359655-70359705	CMK	blood:	n/a
31	chr7:70417419-70417469	SK-N-SH_RA	brain:	n/a
32	chr7:70417419-70417469	IMR90	lung:	fetal
33	chr7:70311532-70311582	HCM	heart:	n/a
34	chr7:70294511-70294561	LNCaP	prostate:	n/a
35	chr7:70294511-70294561	CMK	blood:	n/a
36	chr7:70311532-70311582	HepG2	liver:	n/a
37	chr7:70322401-70322451	HCF	heart:	n/a
38	chr7:70359655-70359705	HNPCEpiC	eye:	n/a
39	chr7:70311321-70311371	SAEC	small airway:	n/a
40	chr7:70294525-70294575	T-47D	breast:	n/a
41	chr7:70359655-70359705	GM12891	blood:	n/a
42	chr7:70294264-70294314	HepG2	liver:	n/a
43	chr7:70311435-70311485	BE2_C	brain:	n/a
44	chr7:70311435-70311485	H1-hESC	embryonic stem cell:	embryo
45	chr7:70322401-70322451	HepG2	liver:	n/a
46	chr7:70311532-70311582	CMK	blood:	n/a
47	chr7:70294525-70294575	ovcar-3	ovarian:	n/a
48	chr7:70322401-70322451	K562	blood:	n/a
49	chr7:70294264-70294314	PrEC	prostate:	n/a
50	chr7:70294525-70294575	AG04449	skin:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70295507..70296249-chr7:71198004..71198896,2	MCF-7	breast:
2	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
3	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
4	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
5	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
6	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
7	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
8	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
9	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
10	chr7:70294117..70295302-chr7:71197788..71199575,6	MCF-7	breast:
11	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
12	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
13	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
14	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
15	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
16	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
17	chr7:70294183..70294797-chr7:71197949..71198693,3	MCF-7	breast:
18	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
19	chr7:70293845..70294790-chr7:71197836..71198902,6	K562	blood:
20	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
21	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
22	chr7:70294046..70294810-chr7:70321629..70322145,2	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
ENSG00000236978	TF binding region
ENSG00000236978	CpG island

Extended variants
information (count: 5099 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5099 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535344888	chr7:70271656-70271657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555528425	chr7:70271689-70271690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142922085	chr7:70271708-70271709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542736649	chr7:70271762-70271763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561009695	chr7:70271766-70271767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180896376	chr7:70271774-70271775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34829794	chr7:70271778-70271779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372032044	chr7:70271789-70271790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1918428	chr7:70271800-70271801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs57275895	chr7:70271834-70271835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs532687435	chr7:70271873-70271874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117343823	chr7:70271876-70271877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374454589	chr7:70271886-70271887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1918427	chr7:70271908-70271909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs536884817	chr7:70271923-70271924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555218196	chr7:70271941-70271942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185154017	chr7:70271945-70271946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13236881	chr7:70272022-70272023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537949380	chr7:70272034-70272035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191592182	chr7:70272044-70272045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13236961	chr7:70272053-70272054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376569297	chr7:70272093-70272094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577612866	chr7:70272147-70272148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538532316	chr7:70272148-70272149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554067954	chr7:70272155-70272156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368018939	chr7:70272156-70272157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557916379	chr7:70272158-70272159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182992917	chr7:70272167-70272168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146098250	chr7:70272212-70272213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560754412	chr7:70272236-70272237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188783789	chr7:70272266-70272267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543552710	chr7:70272286-70272287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370839986	chr7:70272287-70272288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200829423	chr7:70272338-70272339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4463316	chr7:70272341-70272342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191527019	chr7:70272377-70272378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532567811	chr7:70272425-70272426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182754202	chr7:70272429-70272430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568506938	chr7:70272436-70272437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574278084	chr7:70272440-70272441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559963212	chr7:70272447-70272448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187834799	chr7:70272455-70272456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548759582	chr7:70272458-70272459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368681872	chr7:70272479-70272480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13237440	chr7:70272485-70272486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570301950	chr7:70272499-70272500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537935399	chr7:70272503-70272504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534019151	chr7:70272520-70272521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368623201	chr7:70272521-70272522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373299740	chr7:70272549-70272550	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:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70270400-70274000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr7:70273800-70274000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:70273800-70274200	Enhancers	Primary B cells from cord blood	blood
4	chr7:70273800-70274600	ZNF genes & repeats	GM12878-XiMat	blood
5	chr7:70273800-70274800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:70274000-70274400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr7:70274000-70274400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:70274000-70274600	Enhancers	Primary B cells from peripheral blood	blood
9	chr7:70274000-70274600	Enhancers	Dnd41	blood
10	chr7:70274000-70274800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr7:70274000-70275600	Enhancers	Primary T cells from cord blood	blood
12	chr7:70274200-70274400	Enhancers	Primary hematopoietic stem cells	blood
13	chr7:70274200-70276600	Enhancers	Liver	Liver
14	chr7:70274400-70275000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:70274600-70274800	Bivalent Enhancer	Dnd41	blood
16	chr7:70274600-70275800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr7:70275800-70276000	Enhancers	Primary B cells from peripheral blood	blood
18	chr7:70276600-70277000	Weak transcription	Liver	Liver
19	chr7:70277000-70279000	Enhancers	Liver	Liver
20	chr7:70277400-70277800	Enhancers	Fetal Intestine Large	intestine
21	chr7:70277400-70277800	Enhancers	Fetal Intestine Small	intestine
22	chr7:70281400-70281600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr7:70281600-70286600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr7:70285800-70287200	Enhancers	Liver	Liver
25	chr7:70286600-70286800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:70291600-70294400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:70294000-70294200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr7:70294000-70294200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:70294000-70294200	Enhancers	Dnd41	blood
30	chr7:70294000-70294400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
31	chr7:70294000-70294400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:70294000-70294400	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr7:70294000-70294400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
34	chr7:70294000-70294400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:70294000-70294400	Enhancers	Brain Angular Gyrus	brain
36	chr7:70294000-70294400	Active TSS	Brain Anterior Caudate	brain
37	chr7:70294000-70294400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
38	chr7:70294000-70294400	Enhancers	Fetal Brain Male	brain
39	chr7:70294000-70294400	Enhancers	Fetal Muscle Trunk	muscle
40	chr7:70294000-70294400	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr7:70294000-70294400	Bivalent Enhancer	Fetal Stomach	stomach
42	chr7:70294000-70294400	Enhancers	GM12878-XiMat	blood
43	chr7:70294000-70294400	Enhancers	HSMM	muscle
44	chr7:70294000-70294600	Enhancers	HMEC	breast
45	chr7:70294000-70294800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr7:70294000-70295200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
47	chr7:70294000-70296400	Enhancers	Liver	Liver
48	chr7:70294200-70294400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr7:70294200-70294400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:70294200-70294400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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