Variant report

Variant	nsv464712
Chromosome Location	chr7:126881029-126908258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:616)
CpG islands
(count:1466)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:126893656-126894093	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:126891700-126892211	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:126891032-126891379	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr7:126893553-126894248	K562	blood:	n/a	chr7:126893815-126893831
5	BHLHE40	chr7:126898150-126898361	K562	blood:	n/a	n/a
6	BHLHE40	chr7:126893036-126893157	K562	blood:	n/a	chr7:126893111-126893127
7	CBX3	chr7:126893428-126893769	K562	blood:	n/a	n/a
8	CCNT2	chr7:126892999-126894318	K562	blood:	n/a	chr7:126893359-126893368 chr7:126893745-126893754
9	CEBPB	chr7:126891174-126891459	H1-hESC	embryonic stem cell:	n/a	chr7:126891313-126891326
10	CEBPB	chr7:126891146-126891481	K562	blood:	n/a	chr7:126891313-126891326
11	CEBPB	chr7:126891129-126891384	K562	blood:	n/a	chr7:126891313-126891326
12	CEBPB	chr7:126893507-126893665	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:126891143-126891590	A549	lung:	n/a	chr7:126891313-126891326
14	CEBPB	chr7:126893965-126894183	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr7:126892486-126892487	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr7:126893514-126893559	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr7:126891362-126891516	HepG2	liver:	n/a	n/a
18	CHD2	chr7:126893648-126893693	HepG2	liver:	n/a	n/a
19	CHD2	chr7:126894007-126894283	K562	blood:	n/a	n/a
20	CHD2	chr7:126892728-126892855	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr7:126894057-126894267	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr7:126894114-126894157	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr7:126893579-126893719	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr7:126893900-126894288	A549	lung:	n/a	n/a
25	CTBP2	chr7:126891260-126894159	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr7:126891060-126891210	GM12864	blood:	n/a	n/a
27	CTCF	chr7:126893720-126893870	GM12866	blood:	n/a	chr7:126893829-126893842
28	CTCF	chr7:126894060-126894210	HEEpiC	esophagus:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
29	CTCF	chr7:126894040-126894190	GM12873	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
30	CTCF	chr7:126894040-126894190	NHLF	lung:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
31	CTCF	chr7:126892580-126892870	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr7:126894040-126894190	GM06990	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
33	CTCF	chr7:126894060-126894210	MCF-7	breast:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
34	CTCF	chr7:126893888-126894272	H1-hESC	embryonic stem cell:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
35	CTCF	chr7:126893540-126893690	HMEC	breast:	n/a	n/a
36	CTCF	chr7:126894020-126894170	HVMF	connective:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
37	CTCF	chr7:126892680-126892830	HAc	cerebellar:	n/a	n/a
38	CTCF	chr7:126893892-126894296	K562	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
39	CTCF	chr7:126894040-126894190	HepG2	liver:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
40	CTCF	chr7:126891220-126891370	GM12872	blood:	n/a	n/a
41	CTCF	chr7:126894060-126894210	Hela-S3	cervix:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
42	CTCF	chr7:126893840-126893990	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr7:126893580-126893730	HCM	heart:	n/a	n/a
44	CTCF	chr7:126894040-126894190	HFF-Myc	foreskin:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
45	CTCF	chr7:126893932-126894297	K562	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
46	CTCF	chr7:126893540-126893690	GM12871	blood:	n/a	n/a
47	CTCF	chr7:126894080-126894230	K562	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
48	CTCF	chr7:126894020-126894170	SAEC	small airway:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
49	CTCF	chr7:126894060-126894210	GM12868	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
50	CTCF	chr7:126894080-126894230	GM12867	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126882944-126882994	HL-60	blood:	n/a
2	chr7:126897376-126897426	H1-hESC	embryonic stem cell:	embryo
3	chr7:126882944-126882994	HL-60	blood:	n/a
4	chr7:126897376-126897426	H1-hESC	embryonic stem cell:	embryo
5	chr7:126883640-126883690	IMR90	lung:	fetal
6	chr7:126892249-126892299	BE2_C	brain:	n/a
7	chr7:126883640-126883690	NH-A	brain:	n/a
8	chr7:126889015-126889065	CMK	blood:	n/a
9	chr7:126891621-126891671	H1-hESC	embryonic stem cell:	embryo
10	chr7:126897376-126897426	GM06990	blood:	n/a
11	chr7:126884276-126884326	SK-N-MC	brain:	n/a
12	chr7:126892599-126892649	HAEpiC	amniotic membrane:	n/a
13	chr7:126893287-126893337	PrEC	prostate:	n/a
14	chr7:126882944-126882994	Hepatocyte	liver:	n/a
15	chr7:126891621-126891671	PrEC	prostate:	n/a
16	chr7:126890512-126890562	ovcar-3	ovarian:	n/a
17	chr7:126893890-126893940	HIPEpiC	eye:	n/a
18	chr7:126893362-126893412	HRPEpiC	eye:	n/a
19	chr7:126897376-126897426	HIPEpiC	eye:	n/a
20	chr7:126893007-126893057	PFSK-1	brain:	n/a
21	chr7:126891319-126891369	HCT-116	colon:	n/a
22	chr7:126891621-126891671	SKMC	muscle:	n/a
23	chr7:126893237-126893287	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:126883640-126883690	NHBE	bronchial:	n/a
25	chr7:126893237-126893287	GM12878	blood:	n/a
26	chr7:126883640-126883690	HRE	kidney:	n/a
27	chr7:126883137-126883187	PANC-1	pancreas:	n/a
28	chr7:126893304-126893354	MCF-7	breast:	n/a
29	chr7:126893304-126893354	HRCEpiC	kidney:	n/a
30	chr7:126891197-126891247	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:126893237-126893287	HAEpiC	amniotic membrane:	n/a
32	chr7:126891197-126891247	Caco-2	colon:	n/a
33	chr7:126890512-126890562	Hepatocyte	liver:	n/a
34	chr7:126893237-126893287	PFSK-1	brain:	n/a
35	chr7:126893237-126893287	IMR90	lung:	fetal
36	chr7:126890973-126891023	SK-N-SH_RA	brain:	n/a
37	chr7:126882944-126882994	SAEC	small airway:	n/a
38	chr7:126889555-126889605	HRCEpiC	kidney:	n/a
39	chr7:126893362-126893412	HCPEpiC	choroid plexus:	n/a
40	chr7:126893362-126893412	GM12892	blood:	n/a
41	chr7:126892578-126892628	HAEpiC	amniotic membrane:	n/a
42	chr7:126883137-126883187	Caco-2	colon:	n/a
43	chr7:126884276-126884326	NHDF-neo	bronchial:	n/a
44	chr7:126884276-126884326	HL-60	blood:	n/a
45	chr7:126897376-126897426	AG09319	gingival:	n/a
46	chr7:126894250-126894300	GM12892	blood:	n/a
47	chr7:126893007-126893057	HCT-116	colon:	n/a
48	chr7:126893304-126893354	Hela-S3	cervix:	n/a
49	chr7:126882944-126882994	GM06990	blood:	n/a
50	chr7:126885001-126885051	HCPEpiC	choroid plexus:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:126893679..126894246-chr7:127849548..127850071,2	K562	blood:
2	chr7:126875739..126881778-chr7:126881781..126887011,8	K562	blood:
3	chr7:126891985..126894759-chr7:126896631..126899168,2	K562	blood:
4	chr7:126884896..126891192-chr7:126891657..126895737,6	K562	blood:
5	chr7:126879288..126881778-chr7:126885295..126887011,2	K562	blood:
6	chr7:126747288..126748236-chr7:126893729..126894723,2	K562	blood:
7	chr12:52235461..52236089-chr7:126903724..126904354,2	MCF-7	breast:
8	chr7:126893732..126895403-chr7:127004899..127007535,2	K562	blood:
9	chr7:126883585..126886396-chr7:126892877..126894797,2	K562	blood:
10	chr7:126884819..126886507-chr7:126900468..126902207,2	K562	blood:
11	chr7:126887307..126889755-chr7:127030651..127034460,3	MCF-7	breast:
12	chr7:126892951..126894660-chr7:127031651..127034423,2	MCF-7	breast:
13	chr7:126891429..126894759-chr7:127030328..127033331,3	K562	blood:
14	chr7:126884896..126891192-chr7:126891657..126895737,6	K562	blood:
15	chr7:126892205..126895115-chr7:127030974..127032697,2	MCF-7	breast:
16	chr7:126879288..126881778-chr7:126885295..126887011,2	K562	blood:
17	chr7:126894392..126896260-chr7:126987799..126989472,2	K562	blood:
18	chr7:126900301..126902703-chr7:127030705..127032341,2	MCF-7	breast:
19	chr7:126884819..126886507-chr7:126900468..126902207,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-13	chr7:126906423-126906527	NONHSAT123133
2	lnc-ARF5-13	chr7:126904173-126904259	NONHSAT123133
3	lnc-ARF5-13	chr7:126904887-126904958	NONHSAT123133

No data

Variant related genes	Relation type
GRM8	TF binding region
GRM8	CpG island
ENSG00000179603	chromatin interactions
ENSG00000048405	chromatin interactions

Extended variants
information (count: 878 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3779537	chr7:126881029-126881030	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554673230	chr7:126881030-126881031	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs79944514	chr7:126881055-126881056	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185628598	chr7:126881096-126881097	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs149146672	chr7:126881137-126881138	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs571121108	chr7:126881186-126881187	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs13246388	chr7:126881216-126881217	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs547666434	chr7:126881262-126881263	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs377697783	chr7:126881263-126881264	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs544007403	chr7:126881312-126881313	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs554297988	chr7:126881320-126881321	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs569703960	chr7:126881328-126881329	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550170010	chr7:126881348-126881349	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537158975	chr7:126881405-126881406	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559154023	chr7:126881469-126881470	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs566986158	chr7:126881481-126881482	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs202209663	chr7:126881490-126881491	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs17864168	chr7:126881491-126881492	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11291980	chr7:126881492-126881493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs75719926	chr7:126881503-126881504	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs398048107	chr7:126881505-126881506	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541690470	chr7:126881554-126881555	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs17867802	chr7:126881556-126881557	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs139006308	chr7:126881578-126881579	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542180693	chr7:126881647-126881648	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563549857	chr7:126881679-126881680	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190154739	chr7:126881683-126881684	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs7799591	chr7:126881696-126881697	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs17866154	chr7:126881702-126881703	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs564287277	chr7:126881710-126881711	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558526987	chr7:126881736-126881737	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186362674	chr7:126881738-126881739	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs565945011	chr7:126881740-126881741	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376147667	chr7:126881768-126881769	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs187071382	chr7:126883607-126883608	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191564489	chr7:126883613-126883614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375677007	chr7:126883651-126883652	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs139071356	chr7:126883652-126883653	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs61753764	chr7:126883722-126883723	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs147712114	chr7:126883752-126883753	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550978596	chr7:126883791-126883792	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376824644	chr7:126883857-126883858	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373032074	chr7:126883902-126883903	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs201290097	chr7:126883903-126883904	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs17861426	chr7:126883914-126883915	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs117428081	chr7:126884006-126884007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536740933	chr7:126884007-126884008	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs538634252	chr7:126884012-126884013	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368987105	chr7:126884048-126884049	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs183896847	chr7:126884049-126884050	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Prostate cancer	22341455	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126880600-126881400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr7:126884600-126884800	Bivalent Enhancer	Fetal Kidney	kidney
3	chr7:126885000-126885200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
4	chr7:126885200-126885600	Enhancers	Fetal Kidney	kidney
5	chr7:126885400-126885800	Enhancers	Liver	Liver
6	chr7:126885400-126886200	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr7:126885600-126885800	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr7:126885600-126885800	Enhancers	GM12878-XiMat	blood
9	chr7:126885600-126886000	Enhancers	Brain Cingulate Gyrus	brain
10	chr7:126885600-126886000	Flanking Active TSS	Fetal Kidney	kidney
11	chr7:126885800-126886000	Flanking Active TSS	Liver	Liver
12	chr7:126885800-126886000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
13	chr7:126885800-126886000	Flanking Active TSS	GM12878-XiMat	blood
14	chr7:126886000-126886400	Bivalent Enhancer	Fetal Kidney	kidney
15	chr7:126886000-126890400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr7:126886400-126886600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:126887600-126887800	Enhancers	Brain Hippocampus Middle	brain
18	chr7:126887800-126890000	Weak transcription	Brain Hippocampus Middle	brain
19	chr7:126888600-126888800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:126889000-126889200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr7:126889200-126889400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:126889200-126889400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:126889800-126890600	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr7:126890000-126890200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:126890000-126890400	Enhancers	Brain Hippocampus Middle	brain
26	chr7:126890000-126890600	Enhancers	Brain Anterior Caudate	brain
27	chr7:126890200-126890600	Enhancers	Brain Substantia Nigra	brain
28	chr7:126890200-126891000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
29	chr7:126890200-126894400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
30	chr7:126890400-126890600	Enhancers	Brain Cingulate Gyrus	brain
31	chr7:126890400-126890800	Flanking Active TSS	Brain Hippocampus Middle	brain
32	chr7:126890400-126890800	Flanking Bivalent TSS/Enh	Pancreatic Islets	Pancreatic Islet
33	chr7:126890600-126890800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:126890600-126890800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
35	chr7:126890600-126890800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:126890600-126891000	Enhancers	Liver	Liver
37	chr7:126890600-126891000	Active TSS	Brain Cingulate Gyrus	brain
38	chr7:126890600-126891800	Bivalent Enhancer	GM12878-XiMat	blood
39	chr7:126890600-126892000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
40	chr7:126890600-126892000	Active TSS	Brain Anterior Caudate	brain
41	chr7:126890600-126892400	Active TSS	Brain Substantia Nigra	brain
42	chr7:126890600-126894400	Active TSS	Brain Angular Gyrus	brain
43	chr7:126890800-126891000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
44	chr7:126890800-126891000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr7:126890800-126891000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
46	chr7:126890800-126891000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
47	chr7:126890800-126891000	Active TSS	Brain Hippocampus Middle	brain
48	chr7:126890800-126891000	Bivalent/Poised TSS	Fetal Brain Female	brain
49	chr7:126890800-126891000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
50	chr7:126890800-126891200	Bivalent/Poised TSS	Brain Germinal Matrix	brain

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