Variant report

Variant	nsv482430
Chromosome Location	chr4:118347180-118497181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:521)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:118399942-118400139	GM12878	blood:	n/a	n/a
2	CEBPB	chr4:118470821-118471168	IMR90	lung:	n/a	chr4:118470987-118471000 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470987-118471000 chr4:118470989-118471000 chr4:118470989-118470998 chr4:118470987-118470998
3	CEBPB	chr4:118419609-118419809	H1-hESC	embryonic stem cell:	n/a	chr4:118419712-118419723
4	CEBPB	chr4:118466288-118466589	HepG2	liver:	n/a	chr4:118466462-118466473
5	CEBPB	chr4:118388675-118388896	A549	lung:	n/a	chr4:118388751-118388762
6	CEBPB	chr4:118470846-118471144	H1-hESC	embryonic stem cell:	n/a	chr4:118470987-118471000 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470987-118471000 chr4:118470989-118471000 chr4:118470989-118470998 chr4:118470987-118470998
7	CEBPB	chr4:118388582-118388920	IMR90	lung:	n/a	chr4:118388751-118388762
8	CEBPB	chr4:118388743-118388777	K562	blood:	n/a	chr4:118388751-118388762
9	CEBPB	chr4:118377164-118377381	HepG2	liver:	n/a	chr4:118377254-118377265
10	CEBPB	chr4:118470819-118471146	A549	lung:	n/a	chr4:118470987-118471000 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470987-118471000 chr4:118470989-118471000 chr4:118470989-118470998 chr4:118470987-118470998
11	CEBPB	chr4:118470825-118471177	HepG2	liver:	n/a	chr4:118470987-118471000 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470987-118471000 chr4:118470989-118471000 chr4:118470989-118470998 chr4:118470987-118470998
12	CEBPB	chr4:118419537-118419901	HepG2	liver:	n/a	chr4:118419712-118419723
13	CEBPB	chr4:118388589-118388896	HepG2	liver:	n/a	chr4:118388751-118388762
14	CEBPB	chr4:118419534-118419879	IMR90	lung:	n/a	chr4:118419712-118419723
15	CEBPB	chr4:118419554-118419881	A549	lung:	n/a	chr4:118419712-118419723
16	CEBPB	chr4:118486322-118486565	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:118470874-118471170	K562	blood:	n/a	chr4:118470987-118471000 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470989-118470998 chr4:118470987-118471000 chr4:118470989-118471000 chr4:118470989-118470998 chr4:118470987-118470998
18	CTCF	chr4:118369240-118369390	GM12864	blood:	n/a	n/a
19	CTCF	chr4:118350380-118350530	GM12875	blood:	n/a	n/a
20	CTCF	chr4:118369260-118369410	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr4:118350380-118350530	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr4:118481600-118481750	RPTEC	kidney:	n/a	n/a
23	CTCF	chr4:118350400-118350550	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr4:118368900-118369050	GM06990	blood:	n/a	n/a
25	CTCF	chr4:118369380-118369530	GM12868	blood:	n/a	n/a
26	CTCF	chr4:118369240-118369390	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr4:118481620-118481770	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr4:118350440-118350457	GM20000	blood:	n/a	n/a
29	CTCF	chr4:118481460-118481902	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:118369140-118369290	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr4:118350320-118350470	GM12875	blood:	n/a	n/a
32	CTCF	chr4:118481600-118481750	HRE	kidney:	n/a	n/a
33	CTCF	chr4:118497156-118497240	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:118481740-118481890	BE2_C	brain:	n/a	n/a
35	CTCF	chr4:118369265-118369375	ProgFib	skin:	n/a	n/a
36	CTCF	chr4:118369160-118369310	GM12865	blood:	n/a	n/a
37	CTCF	chr4:118369420-118369570	RPTEC	kidney:	n/a	n/a
38	CTCF	chr4:118437580-118437830	BE2_C	brain:	n/a	n/a
39	CTCF	chr4:118481540-118481690	RPTEC	kidney:	n/a	n/a
40	CTCF	chr4:118350320-118350470	GM12869	blood:	n/a	n/a
41	CTCF	chr4:118350300-118350450	GM12873	blood:	n/a	n/a
42	CTCF	chr4:118369200-118369350	K562	blood:	n/a	n/a
43	CTCF	chr4:118437600-118437750	AG04450	lung:	n/a	n/a
44	CTCF	chr4:118369180-118369330	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr4:118369205-118369333	Medullo	brain:	n/a	n/a
46	CTCF	chr4:118481480-118481870	IMR90	lung:	n/a	n/a
47	CTCF	chr4:118481640-118481790	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr4:118350360-118350510	BE2_C	brain:	n/a	n/a
49	CTCF	chr4:118369220-118369370	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr4:118369120-118369270	GM12870	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:118497134-118497184	LNCaP	prostate:	n/a
2	chr4:118497134-118497184	ovcar-3	ovarian:	n/a
3	chr4:118497134-118497184	HRCEpiC	kidney:	n/a
4	chr4:118497134-118497184	SKMC	muscle:	n/a
5	chr4:118497134-118497184	SK-N-MC	brain:	n/a
6	chr4:118497134-118497184	NB4	blood:	n/a
7	chr4:118497134-118497184	H1-hESC	embryonic stem cell:	embryo
8	chr4:118497134-118497184	Hepatocyte	liver:	n/a
9	chr4:118497134-118497184	HAEpiC	amniotic membrane:	n/a
10	chr4:118497134-118497184	SK-N-SH_RA	brain:	n/a
11	chr4:118497134-118497184	HCPEpiC	choroid plexus:	n/a
12	chr4:118497134-118497184	HRE	kidney:	n/a
13	chr4:118497134-118497184	AG04449	skin:	fetal
14	chr4:118497134-118497184	GM19239	blood:	n/a
15	chr4:118497134-118497184	U87	brain:	n/a
16	chr4:118497134-118497184	GM12892	blood:	n/a
17	chr4:118497134-118497184	HMEC	breast:	n/a
18	chr4:118497134-118497184	HCT-116	colon:	n/a
19	chr4:118497134-118497184	AG04450	lung:	fetal
20	chr4:118497134-118497184	ProgFib	skin:	n/a
21	chr4:118497134-118497184	ECC-1	luminal epithelium:	n/a
22	chr4:118497134-118497184	AG09319	gingival:	n/a
23	chr4:118497134-118497184	K562	blood:	n/a
24	chr4:118497134-118497184	HCF	heart:	n/a
25	chr4:118497134-118497184	AG09309	skin:	n/a
26	chr4:118497134-118497184	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:118497134-118497184	MCF10A-Er-Src	breast:	n/a
28	chr4:118497134-118497184	AoSMC	blood vessel:	n/a
29	chr4:118497134-118497184	RPTEC	kidney:	n/a
30	chr4:118497134-118497184	HUVEC	blood vessel:	n/a
31	chr4:118497134-118497184	HNPCEpiC	eye:	n/a
32	chr4:118497134-118497184	GM12878	blood:	n/a
33	chr4:118497134-118497184	Caco-2	colon:	n/a
34	chr4:118497134-118497184	NHBE	bronchial:	n/a
35	chr4:118497134-118497184	IMR90	lung:	fetal
36	chr4:118497134-118497184	PANC-1	pancreas:	n/a
37	chr4:118497134-118497184	T-47D	breast:	n/a
38	chr4:118497134-118497184	Jurkat	blood:	n/a
39	chr4:118497134-118497184	SK-N-SH	brain:	n/a
40	chr4:118497134-118497184	GM12891	blood:	n/a
41	chr4:118497134-118497184	A549	lung:	n/a
42	chr4:118497134-118497184	HRPEpiC	eye:	n/a
43	chr4:118497134-118497184	HEK293	kidney:	embryo
44	chr4:118497134-118497184	AG10803	skin:	n/a
45	chr4:118497134-118497184	BJ	skin:	n/a
46	chr4:118497134-118497184	MCF-7	breast:	n/a
47	chr4:118497134-118497184	NHDF-neo	bronchial:	n/a
48	chr4:118497134-118497184	GM06990	blood:	n/a
49	chr4:118497134-118497184	Hela-S3	cervix:	n/a
50	chr4:118497134-118497184	HCM	heart:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	4:118428948-118429401..4:118541860-118551269	H1-hESC	embryonic stem cell:	embryo
2	4:118387398-118387878..4:118667424-118683756	Hela-S3	cervix:
3	4:118357351-118360885..4:118437019-118438281	H1-hESC	embryonic stem cell:	embryo
4	4:118471614-118473329..4:118473525-118474828	Hela-S3	cervix:
5	4:118357351-118360885..4:118437019-118438281	H1-hESC	embryonic stem cell:	embryo
6	chr4:118377487..118379398-chr4:119198520..119200981,2	K562	blood:
7	chr4:118490388..118492946-chr4:118494495..118496357,2	MCF-7	breast:
8	chr4:118473427..118475701-chr4:118478526..118481071,2	K562	blood:
9	4:118319405-118319911..4:118454469-118464115	H1-hESC	embryonic stem cell:	embryo
10	4:118424109-118425531..4:118428948-118429401	K562	blood:
11	4:118414019-118416561..4:118706981-118715929	Hela-S3	cervix:
12	4:118428948-118429401..4:118429401-118431437	H1-hESC	embryonic stem cell:	embryo
13	chr4:118473427..118475701-chr4:118478526..118481071,2	K562	blood:
14	4:118428948-118429401..4:118429401-118431437	H1-hESC	embryonic stem cell:	embryo
15	4:118357351-118360885..4:118687551-118689447	H1-hESC	embryonic stem cell:	embryo
16	4:118357351-118360885..4:118559839-118566258	GM12878	blood:
17	4:118471614-118473329..4:118473525-118474828	Hela-S3	cervix:
18	4:118454469-118464115..4:118706981-118715929	H1-hESC	embryonic stem cell:	embryo
19	4:118357351-118360885..4:118541860-118551269	H1-hESC	embryonic stem cell:	embryo
20	4:118424109-118425531..4:118428948-118429401	K562	blood:
21	4:118454469-118464115..4:118659345-118667424	H1-hESC	embryonic stem cell:	embryo
22	chr4:118373648..118376261-chr4:118378262..118380604,2	K562	blood:
23	4:118320200-118324249..4:118414019-118416561	Hela-S3	cervix:
24	chr4:118373648..118376261-chr4:118378262..118380604,2	K562	blood:
25	4:118383653-118385442..4:118559839-118566258	H1-hESC	embryonic stem cell:	embryo

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDST3-4	chr4:118349853-118349923	ENSG00000236922.5
2	lnc-TRAM1L1-4	chr4:118461916-118461967	NONHSAT097961
3	lnc-NDST3-4	chr4:118349552-118349639	ENSG00000236922.5
4	lnc-NDST3-4	chr4:118349559-118349639	ENSG00000236922
5	lnc-TRAM1L1-4	chr4:118455201-118455293	NONHSAT097961
6	lnc-NDST3-4	chr4:118461252-118461728	ENSG00000236922
7	lnc-NDST3-4	chr4:118349850-118349923	ENSG00000236922
8	lnc-NDST3-4	chr4:118385627-118385693	ENSG00000236922
9	lnc-NDST3-4	chr4:118492910-118493290	ENSG00000236922.5
10	lnc-NDST3-4	chr4:118389305-118389388	ENSG00000236922
11	lnc-TRAM1L1-4	chr4:118455756-118455837	NONHSAT097961
12	lnc-TRAM1L1-4	chr4:118456449-118456752	NONHSAT097961
13	lnc-TRAM1L1-4	chr4:118491797-118491842	NONHSAT097961

No data

Variant related genes	Relation type
ENSG00000236922	TF binding region
ENSG00000236922	CpG island
ENSG00000236922	chromatin interactions
ENSG00000269893	chromatin interactions

Extended variants
information (count: 2034 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2034 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187835481	chr4:118347212-118347213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570410585	chr4:118347219-118347220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537821663	chr4:118347240-118347241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145653022	chr4:118347243-118347244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534293275	chr4:118347255-118347256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554021755	chr4:118347264-118347265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569263155	chr4:118347285-118347286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs17867070	chr4:118347303-118347304	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs17861893	chr4:118347304-118347305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17861894	chr4:118347305-118347306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs17861895	chr4:118347313-118347314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17865597	chr4:118347332-118347333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60793557	chr4:118347340-118347341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs17874732	chr4:118347341-118347342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553835349	chr4:118347352-118347353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17874734	chr4:118347386-118347387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs17874735	chr4:118347406-118347407	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs190967132	chr4:118347417-118347418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556034618	chr4:118347441-118347442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs59128106	chr4:118347449-118347450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs397826091	chr4:118347456-118347457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147754293	chr4:118347486-118347487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17869432	chr4:118347490-118347491	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs545387480	chr4:118347548-118347549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140924343	chr4:118347563-118347564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541117560	chr4:118347571-118347572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561411096	chr4:118347585-118347586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530315858	chr4:118347595-118347596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550426408	chr4:118347613-118347614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570349922	chr4:118347650-118347651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532661483	chr4:118347679-118347680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527925773	chr4:118347685-118347686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188039016	chr4:118347710-118347711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571110376	chr4:118347736-118347737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533792139	chr4:118347741-118347742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553441864	chr4:118347746-118347747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150185642	chr4:118347758-118347759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540299812	chr4:118347763-118347764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145717120	chr4:118347809-118347810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555973059	chr4:118347834-118347835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75995549	chr4:118347876-118347877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554137858	chr4:118347889-118347890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113593897	chr4:118347920-118347921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13114504	chr4:118347983-118347984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13114547	chr4:118348047-118348048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558813952	chr4:118348058-118348059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114180302	chr4:118348059-118348060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13114776	chr4:118348128-118348129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541464434	chr4:118348133-118348134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191969959	chr4:118348147-118348148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Autism	22495311	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
Melanoma	18172304	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	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
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118339800-118350800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:118350200-118350800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:118350800-118351000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:118355200-118356000	Enhancers	Liver	Liver
5	chr4:118355400-118356000	Enhancers	Fetal Lung	lung
6	chr4:118355600-118356000	Enhancers	Fetal Muscle Leg	muscle
7	chr4:118360400-118360800	Enhancers	Fetal Kidney	kidney
8	chr4:118367600-118370600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:118369200-118369400	Bivalent/Poised TSS	Liver	Liver
10	chr4:118369600-118369800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:118376400-118376800	Enhancers	Liver	Liver
12	chr4:118381600-118382400	Enhancers	Brain Cingulate Gyrus	brain
13	chr4:118381800-118382200	Enhancers	Brain Angular Gyrus	brain
14	chr4:118381800-118382200	Enhancers	Brain Anterior Caudate	brain
15	chr4:118381800-118382400	Enhancers	Brain Substantia Nigra	brain
16	chr4:118381800-118382800	Enhancers	Brain Hippocampus Middle	brain
17	chr4:118381800-118382800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr4:118387200-118388000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:118387200-118388200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:118387200-118388200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:118387200-118388600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:118387200-118388600	Enhancers	HMEC	breast
23	chr4:118387200-118388600	Enhancers	NHEK	skin
24	chr4:118388000-118400800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:118391200-118391800	Enhancers	Dnd41	blood
26	chr4:118391200-118392000	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr4:118391800-118392800	Flanking Active TSS	Dnd41	blood
28	chr4:118392800-118393200	Enhancers	Dnd41	blood
29	chr4:118393200-118396200	Weak transcription	Dnd41	blood
30	chr4:118394600-118394800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:118395000-118396400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:118396200-118396800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:118396200-118397000	Enhancers	Dnd41	blood
34	chr4:118396400-118396600	Enhancers	HMEC	breast
35	chr4:118396400-118396800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:118396400-118396800	Enhancers	NHEK	skin
37	chr4:118396600-118402800	Weak transcription	HMEC	breast
38	chr4:118396800-118399400	Weak transcription	NHEK	skin
39	chr4:118397800-118398200	Enhancers	Fetal Brain Male	brain
40	chr4:118399400-118399800	Enhancers	NHEK	skin
41	chr4:118399400-118401200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:118399800-118400000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:118399800-118402200	Weak transcription	NHEK	skin
44	chr4:118400000-118401200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:118400800-118401200	Enhancers	Left Ventricle	heart
46	chr4:118400800-118401400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:118401200-118401400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr4:118401200-118402400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:118401400-118402400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:118401400-118402800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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