Variant report

Variant	nsv830006
Chromosome Location	chr4:90971656-91186340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1234)
CpG islands
(count:1282)
Chromatin interactive
region (count:95)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:91136473-91136676	HepG2	liver:	n/a	n/a
2	ATF2	chr4:90999554-90999912	GM12878	blood:	n/a	n/a
3	ATF2	chr4:91042996-91043505	GM12878	blood:	n/a	n/a
4	ATF2	chr4:91086989-91087469	GM12878	blood:	n/a	n/a
5	ATF3	chr4:91095768-91096179	HCT-116	colon:	n/a	n/a
6	BACH1	chr4:91031569-91031591	K562	blood:	n/a	n/a
7	BACH1	chr4:91048205-91048813	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:91058764-91059016	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:91049041-91049940	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:91042075-91042239	H1-hESC	embryonic stem cell:	n/a	chr4:91042095-91042109
11	BACH1	chr4:91000545-91000564	K562	blood:	n/a	n/a
12	BATF	chr4:91087025-91087411	GM12878	blood:	n/a	n/a
13	BATF	chr4:91087040-91087440	GM12878	blood:	n/a	n/a
14	BATF	chr4:90999666-90999978	GM12878	blood:	n/a	chr4:90999790-90999801
15	BATF	chr4:91108443-91108773	GM12878	blood:	n/a	n/a
16	BATF	chr4:91132349-91132742	GM12878	blood:	n/a	chr4:91132567-91132578
17	BATF	chr4:90999669-90999978	GM12878	blood:	n/a	chr4:90999790-90999801
18	BATF	chr4:91108455-91108750	GM12878	blood:	n/a	n/a
19	BATF	chr4:91021041-91021196	GM12878	blood:	n/a	chr4:91021128-91021139 chr4:91021142-91021153
20	BCL11A	chr4:91108495-91108764	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:91001263-91001504	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:91108420-91108790	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:91087131-91087411	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:91087042-91087408	GM12878	blood:	n/a	n/a
25	BCL3	chr4:91043481-91043888	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:91049447-91049983	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:91048397-91049079	GM12878	blood:	n/a	chr4:91049042-91049058
28	BHLHE40	chr4:91087085-91087452	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:91136458-91136793	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:91144753-91144762	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:91063577-91063585	GM12878	blood:	n/a	n/a
32	BRCA1	chr4:91049004-91049024	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr4:91043669-91043689	GM12878	blood:	n/a	n/a
34	CBX3	chr4:91095667-91096416	HCT-116	colon:	n/a	n/a
35	CEBPB	chr4:91039703-91039966	A549	lung:	n/a	n/a
36	CEBPB	chr4:91025213-91025517	Hela-S3	cervix:	n/a	chr4:91025372-91025385 chr4:91025373-91025384
37	CEBPB	chr4:91081200-91081761	MCF-7	breast:	n/a	n/a
38	CEBPB	chr4:91095604-91096368	MCF-7	breast:	n/a	n/a
39	CEBPB	chr4:90979379-90979524	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:91049757-91050097	IMR90	lung:	n/a	chr4:91049926-91049939
41	CEBPB	chr4:91136568-91136686	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:91039710-91039949	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:91039696-91039943	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:91084308-91084540	A549	lung:	n/a	n/a
45	CEBPB	chr4:90979291-90979568	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:91048013-91048213	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr4:91030301-91030451	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:91095569-91096407	MCF-7	breast:	n/a	n/a
49	CEBPB	chr4:91061300-91061621	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr4:91049567-91050208	ECC-1	luminal epithelium:	n/a	chr4:91049926-91049939

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:91048567-91048617	BJ	skin:	n/a
2	chr4:91048567-91048617	BJ	skin:	n/a
3	chr4:91048916-91048966	HMEC	breast:	n/a
4	chr4:91048584-91048634	HCT-116	colon:	n/a
5	chr4:91048567-91048617	NB4	blood:	n/a
6	chr4:91048559-91048609	K562	blood:	n/a
7	chr4:91048419-91048469	ProgFib	skin:	n/a
8	chr4:91048416-91048466	AG09309	skin:	n/a
9	chr4:91047852-91047902	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:91052378-91052428	IMR90	lung:	fetal
11	chr4:91048416-91048466	ovcar-3	ovarian:	n/a
12	chr4:91045103-91045153	HCM	heart:	n/a
13	chr4:91048557-91048607	HepG2	liver:	n/a
14	chr4:91049728-91049778	K562	blood:	n/a
15	chr4:91156040-91156090	NB4	blood:	n/a
16	chr4:91048567-91048617	HCF	heart:	n/a
17	chr4:91052378-91052428	SAEC	small airway:	n/a
18	chr4:91049645-91049695	AoSMC	blood vessel:	n/a
19	chr4:91049728-91049778	HUVEC	blood vessel:	n/a
20	chr4:91156290-91156340	PFSK-1	brain:	n/a
21	chr4:91047852-91047902	K562	blood:	n/a
22	chr4:91048916-91048966	U87	brain:	n/a
23	chr4:91049645-91049695	NB4	blood:	n/a
24	chr4:91156040-91156090	SAEC	small airway:	n/a
25	chr4:91048557-91048607	SK-N-MC	brain:	n/a
26	chr4:91156113-91156163	GM12892	blood:	n/a
27	chr4:91156113-91156163	ovcar-3	ovarian:	n/a
28	chr4:91048584-91048634	GM12892	blood:	n/a
29	chr4:91045103-91045153	HNPCEpiC	eye:	n/a
30	chr4:91156155-91156205	NT2-D1	testis:	n/a
31	chr4:91149045-91149095	NHDF-neo	bronchial:	n/a
32	chr4:91048916-91048966	HEK293	kidney:	embryo
33	chr4:91048557-91048607	HCPEpiC	choroid plexus:	n/a
34	chr4:91156290-91156340	HCT-116	colon:	n/a
35	chr4:91048584-91048634	AG09309	skin:	n/a
36	chr4:91048559-91048609	U87	brain:	n/a
37	chr4:91047852-91047902	Hepatocyte	liver:	n/a
38	chr4:91156040-91156090	GM12891	blood:	n/a
39	chr4:91048419-91048469	HL-60	blood:	n/a
40	chr4:91156155-91156205	HepG2	liver:	n/a
41	chr4:91156113-91156163	HRE	kidney:	n/a
42	chr4:91156113-91156163	HRCEpiC	kidney:	n/a
43	chr4:91047852-91047902	HCF	heart:	n/a
44	chr4:91048416-91048466	HNPCEpiC	eye:	n/a
45	chr4:91048419-91048469	SKMC	muscle:	n/a
46	chr4:91048823-91048873	GM19239	blood:	n/a
47	chr4:91049533-91049583	GM19239	blood:	n/a
48	chr4:91048567-91048617	AG04450	lung:	fetal
49	chr4:91047852-91047902	HAEpiC	amniotic membrane:	n/a
50	chr4:91156113-91156163	Caco-2	colon:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:91038578..91040695-chr4:91044808..91046326,2	K562	blood:
2	chr4:91079050..91083198-chr4:91093894..91096382,3	MCF-7	breast:
3	chr4:91062775..91065678-chr4:91069290..91071948,2	MCF-7	breast:
4	chr4:91053948..91055557-chr4:91062893..91064405,2	MCF-7	breast:
5	chr4:91025999..91028875-chr7:61969348..61970976,2	MCF-7	breast:
6	chr4:91048019..91050681-chr4:91168667..91171182,2	MCF-7	breast:
7	chr4:91081266..91083845-chr4:91092488..91096504,5	MCF-7	breast:
8	chr4:91058460..91060722-chr4:91062394..91065261,3	MCF-7	breast:
9	chr4:91047203..91056216-chr4:91079211..91084756,17	MCF-7	breast:
10	chr4:91047666..91049579-chr4:91159621..91163090,3	MCF-7	breast:
11	chr4:91079050..91083198-chr4:91093894..91096382,3	MCF-7	breast:
12	chr4:91051066..91053200-chr4:91063053..91065601,2	MCF-7	breast:
13	chr4:91090113..91093014-chr4:91094253..91096344,2	MCF-7	breast:
14	chr4:91095343..91097484-chr4:91102643..91104635,3	MCF-7	breast:
15	chr4:91051312..91053951-chr4:91079435..91081178,2	MCF-7	breast:
16	chr4:91038578..91040695-chr4:91044808..91046326,2	K562	blood:
17	chr4:91058102..91060514-chr4:91081262..91083750,2	MCF-7	breast:
18	chr4:91049244..91050799-chr4:91210980..91212924,2	MCF-7	breast:
19	chr4:91090113..91093014-chr4:91094253..91096344,2	MCF-7	breast:
20	chr4:91048663..91049547-chr4:91095789..91096328,2	MCF-7	breast:
21	chr4:90979793..90982675-chr4:91045572..91048422,2	MCF-7	breast:
22	chr4:91098831..91102400-chr4:91107019..91110825,3	K562	blood:
23	chr4:91052874..91054411-chr4:91106390..91108786,2	MCF-7	breast:
24	chr4:91081506..91083784-chr4:91211586..91214235,2	MCF-7	breast:
25	chr4:91068997..91071513-chr4:91093678..91096479,3	MCF-7	breast:
26	chr4:91007942..91012352-chr4:91047330..91049879,3	MCF-7	breast:
27	chr4:91068997..91071513-chr4:91093678..91096479,3	MCF-7	breast:
28	chr4:91073236..91073889-chr4:91214194..91215162,2	MCF-7	breast:
29	chr4:91048485..91049157-chr9:101983883..101984451,2	Hela-S3	cervix:
30	chr12:95854714..95855676-chr4:91048972..91049512,2	HCT-116	colon:
31	chr4:91079283..91080905-chr4:91104406..91107229,2	MCF-7	breast:
32	chr4:91047507..91050919-chr4:91101707..91107580,10	MCF-7	breast:
33	chr4:91047815..91052213-chr4:91059218..91065616,9	MCF-7	breast:
34	chr4:91047994..91050981-chr4:91052032..91057760,8	MCF-7	breast:
35	chr17:56754989..56757359-chr4:91049583..91051351,2	MCF-7	breast:
36	chr1:55861688..55862189-chr4:91116829..91117329,2	Hela-S3	cervix:
37	chr4:91047084..91051419-chr4:91092902..91098296,11	MCF-7	breast:
38	chr4:91046411..91048761-chr4:91112912..91114685,2	MCF-7	breast:
39	chr4:91048863..91050461-chr4:91183370..91185880,2	MCF-7	breast:
40	chr4:91048643..91051024-chr4:91179121..91181486,2	MCF-7	breast:
41	chr4:91078608..91080610-chr4:91086840..91091060,3	MCF-7	breast:
42	chr4:91048424..91050386-chr4:91115679..91118506,2	MCF-7	breast:
43	chr4:91068584..91070766-chr4:91072212..91073910,2	MCF-7	breast:
44	chr4:91052874..91054411-chr4:91106390..91108786,2	MCF-7	breast:
45	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
46	chr4:91086785..91089901-chr4:91092101..91094154,3	MCF-7	breast:
47	chr4:91048337..91050046-chr4:91171503..91174117,2	MCF-7	breast:
48	chr4:91051312..91053951-chr4:91079435..91081178,2	MCF-7	breast:
49	chr4:91047346..91051064-chr4:91103358..91108092,8	MCF-7	breast:
50	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:

No data

Variant related genes	Relation type
CCSER1	TF binding region
CCSER1	CpG island
ENSG00000167962	chromatin interactions
ENSG00000233246	chromatin interactions
ENSG00000164292	chromatin interactions
ENSG00000106803	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000206917	chromatin interactions
ENSG00000184305	chromatin interactions
ENSG00000119523	chromatin interactions
ENSG00000134686	chromatin interactions
ENSG00000183971	chromatin interactions

Extended variants
information (count: 6384 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6384 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs722937	chr4:90971745-90971746	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574600237	chr4:90971762-90971763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543576696	chr4:90971766-90971767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563448556	chr4:90971768-90971769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369621666	chr4:90971769-90971770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72874319	chr4:90971782-90971783	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs546067463	chr4:90971789-90971790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559394855	chr4:90971798-90971799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528442758	chr4:90971799-90971800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs722936	chr4:90971800-90971801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs151334964	chr4:90971811-90971812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12500465	chr4:90971832-90971833	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs534682149	chr4:90971854-90971855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140592442	chr4:90971860-90971861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570707436	chr4:90971880-90971881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577663770	chr4:90971891-90971892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113233236	chr4:90971966-90971967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553590933	chr4:90971969-90971970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76046705	chr4:90972013-90972014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72874321	chr4:90972021-90972022	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs554252830	chr4:90972085-90972086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541657287	chr4:90972133-90972134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187763243	chr4:90972142-90972143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192328049	chr4:90972204-90972205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377058858	chr4:90972291-90972292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545680236	chr4:90972300-90972301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559572515	chr4:90972306-90972307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73831907	chr4:90972347-90972348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs563617560	chr4:90972348-90972349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72874323	chr4:90972385-90972386	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs561728727	chr4:90972400-90972401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575596063	chr4:90972457-90972458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13124133	chr4:90972536-90972537	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs145907424	chr4:90972546-90972547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570808467	chr4:90972548-90972549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564250389	chr4:90972558-90972559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533540685	chr4:90972601-90972602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546892214	chr4:90972643-90972644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564436826	chr4:90972644-90972645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528584939	chr4:90972646-90972647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184664574	chr4:90972670-90972671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535751723	chr4:90972686-90972687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549741539	chr4:90972687-90972688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568050152	chr4:90972768-90972769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79829084	chr4:90972798-90972799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557046654	chr4:90972799-90972800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138717557	chr4:90972842-90972843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13151441	chr4:90972844-90972845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs142716883	chr4:90972892-90972893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573024176	chr4:90972925-90972926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
lymphocytic leukemia	21291569	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
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Parkinson disease	17953491	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495309	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90964000-90973400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr4:90966200-90973400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:90973200-90973600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr4:90973200-90974200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr4:90973200-90974200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:90973400-90973800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr4:90973400-90974000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:90973400-90974200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:90973400-90974200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:90973400-90974200	Enhancers	Brain Germinal Matrix	brain
11	chr4:90973400-90974400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr4:90973400-90974600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr4:90973400-90974800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr4:90973600-90974400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:90978600-90978800	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr4:90981200-90981600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:90981200-90981600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:90981200-90981600	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:90981200-90981800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:90981400-90981600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:90981600-90983000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr4:90981600-90985000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr4:90981600-90985400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr4:90981800-90983000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr4:90983000-90983400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr4:90983000-90983400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:90983000-90983400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:90983000-90983400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr4:90983000-90983800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:90983200-90984000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr4:90983400-90985200	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr4:90983400-90985400	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr4:90983400-90985400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:90983800-90985400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr4:90985000-90985600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr4:90985000-90985600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:90985400-90985600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:90985400-90985600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:90985400-90985600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr4:90985400-90985800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr4:90985600-90985800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr4:90986200-90986600	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr4:90986400-90986800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:90989800-90990800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:90990000-90990600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:90990000-90990800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:90990000-90990800	Enhancers	HMEC	breast
48	chr4:90990000-90990800	Enhancers	NHEK	skin
49	chr4:90990800-90999800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:90992000-90993200	Enhancers	Primary monocytes fromperipheralblood	blood

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