Variant report

Variant	nsv1017325
Chromosome Location	chr4:128408370-128509276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:778)
CpG islands
(count:184)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:778 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:128446821-128447141	K562	blood:	n/a	n/a
2	ARID3A	chr4:128454597-128454833	K562	blood:	n/a	n/a
3	ARID3A	chr4:128438475-128438545	K562	blood:	n/a	n/a
4	ARID3A	chr4:128460128-128460277	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:128460020-128460281	K562	blood:	n/a	n/a
6	ARID3A	chr4:128508162-128508384	K562	blood:	n/a	n/a
7	ARID3A	chr4:128426459-128426608	K562	blood:	n/a	n/a
8	ATF1	chr4:128422271-128422576	K562	blood:	n/a	n/a
9	ATF1	chr4:128446814-128447100	K562	blood:	n/a	n/a
10	ATF1	chr4:128454392-128454859	K562	blood:	n/a	n/a
11	BHLHE40	chr4:128436599-128436691	K562	blood:	n/a	n/a
12	BHLHE40	chr4:128454410-128454963	K562	blood:	n/a	n/a
13	BHLHE40	chr4:128460072-128460251	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:128446814-128446968	K562	blood:	n/a	n/a
15	BRCA1	chr4:128460025-128460358	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr4:128451304-128451648	K562	blood:	n/a	n/a
17	CBX3	chr4:128436438-128436818	K562	blood:	n/a	n/a
18	CBX3	chr4:128454556-128454882	K562	blood:	n/a	n/a
19	CCNT2	chr4:128426346-128426656	K562	blood:	n/a	n/a
20	CCNT2	chr4:128454291-128454871	K562	blood:	n/a	chr4:128454772-128454792
21	CEBPB	chr4:128421118-128421321	HepG2	liver:	n/a	chr4:128421178-128421189
22	CEBPB	chr4:128454578-128454866	K562	blood:	n/a	chr4:128454630-128454643
23	CEBPB	chr4:128408896-128409099	K562	blood:	n/a	chr4:128408965-128408976
24	CEBPB	chr4:128479070-128479295	HepG2	liver:	n/a	chr4:128479194-128479205
25	CEBPB	chr4:128412785-128413068	HepG2	liver:	n/a	chr4:128412940-128412951 chr4:128412922-128412933
26	CEBPB	chr4:128425773-128426012	K562	blood:	n/a	n/a
27	CEBPB	chr4:128445594-128445796	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:128434631-128434836	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:128487089-128487289	IMR90	lung:	n/a	chr4:128487206-128487217
30	CEBPB	chr4:128412781-128413072	K562	blood:	n/a	chr4:128412940-128412951 chr4:128412922-128412933
31	CEBPB	chr4:128444575-128444819	K562	blood:	n/a	n/a
32	CEBPB	chr4:128412903-128413083	H1-hESC	embryonic stem cell:	n/a	chr4:128412940-128412951 chr4:128412922-128412933
33	CEBPB	chr4:128508025-128508188	A549	lung:	n/a	n/a
34	CEBPB	chr4:128408922-128409122	HepG2	liver:	n/a	chr4:128408965-128408976
35	CEBPB	chr4:128408958-128409147	A549	lung:	n/a	chr4:128408965-128408976
36	CEBPB	chr4:128487097-128487297	HepG2	liver:	n/a	chr4:128487206-128487217
37	CEBPB	chr4:128445581-128445854	K562	blood:	n/a	n/a
38	CEBPB	chr4:128507890-128508128	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:128479181-128479305	K562	blood:	n/a	chr4:128479194-128479205
40	CEBPB	chr4:128445643-128445788	A549	lung:	n/a	n/a
41	CEBPD	chr4:128454610-128455015	K562	blood:	n/a	n/a
42	CHD1	chr4:128459750-128460780	IMR90	lung:	n/a	n/a
43	CTCF	chr4:128508240-128508390	HepG2	liver:	n/a	n/a
44	CTCF	chr4:128460100-128460250	BJ	skin:	n/a	chr4:128460141-128460154 chr4:128460139-128460157 chr4:128460145-128460154
45	CTCF	chr4:128487138-128487202	GM13977	blood:	n/a	n/a
46	CTCF	chr4:128460022-128460272	Fibrobl	skin:	n/a	chr4:128460141-128460154 chr4:128460139-128460157 chr4:128460145-128460154
47	CTCF	chr4:128508200-128508350	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr4:128508240-128508390	AG10803	skin:	n/a	n/a
49	CTCF	chr4:128460060-128460210	AG04449	skin:	n/a	chr4:128460141-128460154 chr4:128460139-128460157 chr4:128460145-128460154
50	CTCF	chr4:128508240-128508390	GM12801	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128440118-128440168	SK-N-SH_RA	brain:	n/a
2	chr4:128440118-128440168	SK-N-SH_RA	brain:	n/a
3	chr4:128461763-128461813	HCT-116	colon:	n/a
4	chr4:128461763-128461813	HCF	heart:	n/a
5	chr4:128461763-128461813	HCPEpiC	choroid plexus:	n/a
6	chr4:128430108-128430158	HRPEpiC	eye:	n/a
7	chr4:128440118-128440168	CMK	blood:	n/a
8	chr4:128461763-128461813	Hepatocyte	liver:	n/a
9	chr4:128440118-128440168	HRE	kidney:	n/a
10	chr4:128440118-128440168	U87	brain:	n/a
11	chr4:128430108-128430158	HEK293	kidney:	embryo
12	chr4:128440118-128440168	AG09309	skin:	n/a
13	chr4:128461763-128461813	HRPEpiC	eye:	n/a
14	chr4:128430108-128430158	AG04450	lung:	fetal
15	chr4:128461763-128461813	AG04449	skin:	fetal
16	chr4:128430108-128430158	RPTEC	kidney:	n/a
17	chr4:128430108-128430158	HIPEpiC	eye:	n/a
18	chr4:128461763-128461813	RPTEC	kidney:	n/a
19	chr4:128440118-128440168	A549	lung:	n/a
20	chr4:128461763-128461813	IMR90	lung:	fetal
21	chr4:128440118-128440168	HCPEpiC	choroid plexus:	n/a
22	chr4:128440118-128440168	HCT-116	colon:	n/a
23	chr4:128430108-128430158	BE2_C	brain:	n/a
24	chr4:128430108-128430158	CMK	blood:	n/a
25	chr4:128461763-128461813	MCF-7	breast:	n/a
26	chr4:128461763-128461813	A549	lung:	n/a
27	chr4:128461763-128461813	SKMC	muscle:	n/a
28	chr4:128440118-128440168	PFSK-1	brain:	n/a
29	chr4:128440118-128440168	RPTEC	kidney:	n/a
30	chr4:128430108-128430158	T-47D	breast:	n/a
31	chr4:128440118-128440168	T-47D	breast:	n/a
32	chr4:128461763-128461813	HRE	kidney:	n/a
33	chr4:128430108-128430158	SKMC	muscle:	n/a
34	chr4:128430108-128430158	SK-N-MC	brain:	n/a
35	chr4:128440118-128440168	GM12891	blood:	n/a
36	chr4:128461763-128461813	Caco-2	colon:	n/a
37	chr4:128440118-128440168	HAEpiC	amniotic membrane:	n/a
38	chr4:128440118-128440168	SAEC	small airway:	n/a
39	chr4:128430108-128430158	HUVEC	blood vessel:	n/a
40	chr4:128440118-128440168	HUVEC	blood vessel:	n/a
41	chr4:128440118-128440168	HNPCEpiC	eye:	n/a
42	chr4:128440118-128440168	MCF10A-Er-Src	breast:	n/a
43	chr4:128440118-128440168	AG09319	gingival:	n/a
44	chr4:128430108-128430158	PrEC	prostate:	n/a
45	chr4:128461763-128461813	HNPCEpiC	eye:	n/a
46	chr4:128440118-128440168	NH-A	brain:	n/a
47	chr4:128461763-128461813	GM06990	blood:	n/a
48	chr4:128440118-128440168	Hela-S3	cervix:	n/a
49	chr4:128430108-128430158	HRCEpiC	kidney:	n/a
50	chr4:128461763-128461813	ProgFib	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:128375252..128378171-chr4:128454899..128457356,2	K562	blood:
2	chr4:128449705..128452234-chr4:128453227..128455144,2	K562	blood:
3	chr4:128486825..128490042-chr4:128490605..128492933,3	K562	blood:
4	chr4:128497413..128500074-chr4:128505896..128508169,2	MCF-7	breast:
5	chr4:128438189..128441215-chr4:128442876..128446018,3	K562	blood:
6	chr4:128438189..128441215-chr4:128442876..128446018,3	K562	blood:
7	chr4:128449129..128451520-chr4:128453107..128455386,2	K562	blood:
8	chr4:128449129..128451520-chr4:128453107..128455386,2	K562	blood:
9	chr4:128459720..128460439-chr4:128507855..128508488,3	MCF-7	breast:
10	chr3:119865708..119866577-chr4:128412232..128412732,2	MCF-7	breast:
11	chr4:128486825..128490042-chr4:128490605..128492933,3	K562	blood:
12	chr4:128490719..128492998-chr4:128553129..128556082,2	K562	blood:
13	chr4:128449705..128452234-chr4:128453227..128455144,2	K562	blood:
14	chr4:128459720..128460439-chr4:128507855..128508488,3	MCF-7	breast:
15	chr4:128497413..128500074-chr4:128505896..128508169,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTU-1	chr4:128419482-128419962	NONHSAT098238
2	lnc-INTU-2	chr4:128414660-128414983	NONHSAT098237
3	lnc-MFSD8-9	chr4:128492862-128492960	l_2728_chr4:128237735-128492960_lung

No data

Variant related genes	Relation type
ENSG00000248209	TF binding region
ENSG00000249795	TF binding region
ENSG00000248209	CpG island
ENSG00000249795	CpG island
ENSG00000164066	chromatin interactions

Extended variants
information (count: 2690 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2690 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534964334	chr4:128408450-128408451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571384770	chr4:128408460-128408461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528894426	chr4:128408466-128408467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574029430	chr4:128408486-128408487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539524032	chr4:128408503-128408504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186986572	chr4:128408521-128408522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576191039	chr4:128408523-128408524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79555190	chr4:128408622-128408623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562356608	chr4:128408695-128408696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574244025	chr4:128408769-128408770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541747096	chr4:128408770-128408771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142088647	chr4:128408877-128408878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72680096	chr4:128408879-128408880	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs551459374	chr4:128408995-128408996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535465810	chr4:128409008-128409009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112324430	chr4:128409063-128409064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555298901	chr4:128409085-128409086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79001659	chr4:128409107-128409108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs151168050	chr4:128409172-128409173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538305174	chr4:128409173-128409174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191826590	chr4:128409267-128409268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184108123	chr4:128409271-128409272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546516949	chr4:128409288-128409289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2137866	chr4:128409302-128409303	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs13136353	chr4:128409339-128409340	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112972829	chr4:128409370-128409371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187509311	chr4:128409376-128409377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570048775	chr4:128409446-128409447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537595821	chr4:128409465-128409466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540465523	chr4:128409492-128409493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554542904	chr4:128409568-128409569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574343919	chr4:128409588-128409589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375525435	chr4:128409594-128409595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547372538	chr4:128409624-128409625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189627444	chr4:128409708-128409709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553717326	chr4:128409711-128409712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138051838	chr4:128409745-128409746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562439188	chr4:128409829-128409830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377665394	chr4:128409857-128409858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542788792	chr4:128409861-128409862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182303761	chr4:128409911-128409912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs72680097	chr4:128409925-128409926	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs908010	chr4:128409926-128409927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530512106	chr4:128409951-128409952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115475026	chr4:128409964-128409965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560897051	chr4:128409975-128409976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545117602	chr4:128409984-128409985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186961986	chr4:128409996-128409997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546449610	chr4:128410046-128410047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114490965	chr4:128410092-128410093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128405600-128408600	Enhancers	Fetal Heart	heart
2	chr4:128407400-128410600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:128407600-128409400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:128407600-128409400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr4:128407600-128409600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr4:128407600-128409600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:128407800-128408400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:128409400-128410000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:128409400-128411000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:128409600-128409800	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:128409600-128409800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr4:128409600-128410800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:128409600-128410800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr4:128410400-128410600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr4:128410600-128411000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:128412200-128413600	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr4:128419200-128422400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:128419400-128419800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:128419800-128421600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:128419800-128422800	Enhancers	Fetal Heart	heart
21	chr4:128421600-128422000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:128421600-128422800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr4:128421600-128423000	Enhancers	Fetal Lung	lung
24	chr4:128421800-128422600	Enhancers	Ovary	ovary
25	chr4:128421800-128422800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr4:128421800-128422800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:128421800-128422800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr4:128421800-128422800	Enhancers	NH-A	brain
29	chr4:128421800-128424000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:128422000-128422200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr4:128422000-128422600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:128422000-128422600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:128422000-128422600	Enhancers	Fetal Muscle Leg	muscle
34	chr4:128422000-128422600	Enhancers	Left Ventricle	heart
35	chr4:128422000-128422600	Enhancers	Right Ventricle	heart
36	chr4:128422000-128422800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr4:128422000-128422800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:128422000-128422800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:128422000-128423000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr4:128422000-128423000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:128422000-128424800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr4:128422000-128424800	Enhancers	NHDF-Ad	bronchial
43	chr4:128422000-128426000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:128422200-128422600	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr4:128422200-128422600	Enhancers	K562	blood
46	chr4:128422200-128422800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr4:128422200-128422800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:128422200-128423600	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr4:128422400-128422800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:128422400-128422800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links