Variant report

Variant	nsv1000173
Chromosome Location	chr4:100928002-100964404
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:156)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:156 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:100938971-100939519	GM12878	blood:	n/a	n/a
2	BATF	chr4:100939136-100939419	GM12878	blood:	n/a	chr4:100939291-100939302
3	BCL11A	chr4:100939119-100939389	GM12878	blood:	n/a	n/a
4	BCL3	chr4:100939066-100939443	GM12878	blood:	n/a	n/a
5	CBX3	chr4:100939031-100939518	HCT-116	colon:	n/a	n/a
6	CEBPB	chr4:100928161-100928305	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:100939109-100939483	HCT-116	colon:	n/a	n/a
8	CEBPB	chr4:100963505-100963729	K562	blood:	n/a	chr4:100963581-100963592
9	CEBPB	chr4:100963414-100963758	Hela-S3	cervix:	n/a	chr4:100963581-100963592
10	CEBPB	chr4:100940739-100940779	HepG2	liver:	n/a	chr4:100940756-100940767 chr4:100940756-100940769
11	CEBPB	chr4:100929292-100929565	A549	lung:	n/a	chr4:100929418-100929429
12	CEBPB	chr4:100963431-100963759	HepG2	liver:	n/a	chr4:100963581-100963592
13	CEBPB	chr4:100963410-100963778	IMR90	lung:	n/a	chr4:100963581-100963592
14	CEBPB	chr4:100929230-100929608	IMR90	lung:	n/a	chr4:100929418-100929429
15	CEBPB	chr4:100937295-100937685	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:100963434-100963755	A549	lung:	n/a	chr4:100963581-100963592
17	CTCF	chr4:100937295-100937621	IMR90	lung:	n/a	n/a
18	CTCF	chr4:100937340-100937490	AG09319	gingival:	n/a	n/a
19	CTCF	chr4:100937460-100937610	BJ	skin:	n/a	n/a
20	CTCF	chr4:100937440-100937590	HPF	lung:	n/a	n/a
21	CTCF	chr4:100937360-100937510	HPF	lung:	n/a	n/a
22	CTCF	chr4:100937360-100937510	AG09319	gingival:	n/a	n/a
23	CTCF	chr4:100937340-100937490	AG04450	lung:	n/a	n/a
24	CTCF	chr4:100937300-100937450	BJ	skin:	n/a	n/a
25	CTCF	chr4:100937320-100937470	NHDF-neo	bronchial:	n/a	n/a
26	EP300	chr4:100939014-100939047	K562	blood:	n/a	n/a
27	EP300	chr4:100942843-100945025	SK-N-SH	brain:	n/a	chr4:100944809-100944819 chr4:100943284-100943294
28	EP300	chr4:100943836-100944410	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr4:100943806-100944376	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr4:100939198-100939398	GM12878	blood:	n/a	n/a
31	FOS	chr4:100962797-100963156	MCF10A-Er-Src	breast:	n/a	chr4:100962955-100962967 chr4:100962840-100962852 chr4:100962961-100962970 chr4:100962960-100962972 chr4:100962962-100962971
32	FOS	chr4:100929412-100929436	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr4:100962803-100963147	MCF10A-Er-Src	breast:	n/a	chr4:100962955-100962967 chr4:100962840-100962852 chr4:100962961-100962970 chr4:100962960-100962972 chr4:100962962-100962971
34	FOS	chr4:100929283-100929553	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:100939033-100939548	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:100963437-100963626	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr4:100963449-100963737	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:100929353-100929618	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:100962791-100963142	MCF10A-Er-Src	breast:	n/a	chr4:100962955-100962967 chr4:100962840-100962852 chr4:100962961-100962970 chr4:100962960-100962972 chr4:100962962-100962971
40	FOS	chr4:100935876-100936031	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:100939022-100939548	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:100939076-100939477	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:100962799-100963139	MCF10A-Er-Src	breast:	n/a	chr4:100962955-100962967 chr4:100962840-100962852 chr4:100962961-100962970 chr4:100962960-100962972 chr4:100962962-100962971
44	FOS	chr4:100929327-100929570	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr4:100938853-100939570	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL1	chr4:100939004-100939447	HCT-116	colon:	n/a	n/a
47	FOSL1	chr4:100938948-100939593	HCT-116	colon:	n/a	n/a
48	FOSL2	chr4:100939166-100939448	MCF-7	breast:	n/a	n/a
49	FOXA1	chr4:100939078-100939442	A549	lung:	n/a	n/a
50	FOXA1	chr4:100939002-100939351	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100963223-100963273	AG04450	lung:	fetal
2	chr4:100937264-100937314	SK-N-SH	brain:	n/a
3	chr4:100937264-100937314	HIPEpiC	eye:	n/a
4	chr4:100963223-100963273	CMK	blood:	n/a
5	chr4:100937264-100937314	Hepatocyte	liver:	n/a
6	chr4:100963223-100963273	AoSMC	blood vessel:	n/a
7	chr4:100937264-100937314	BJ	skin:	n/a
8	chr4:100963223-100963273	PANC-1	pancreas:	n/a
9	chr4:100963223-100963273	ovcar-3	ovarian:	n/a
10	chr4:100937264-100937314	A549	lung:	n/a
11	chr4:100937264-100937314	Caco-2	colon:	n/a
12	chr4:100963223-100963273	HMEC	breast:	n/a
13	chr4:100937264-100937314	HRPEpiC	eye:	n/a
14	chr4:100937264-100937314	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:100963223-100963273	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:100937264-100937314	HCT-116	colon:	n/a
17	chr4:100963223-100963273	SK-N-SH_RA	brain:	n/a
18	chr4:100963223-100963273	IMR90	lung:	fetal
19	chr4:100937264-100937314	K562	blood:	n/a
20	chr4:100937264-100937314	HRCEpiC	kidney:	n/a
21	chr4:100963223-100963273	GM06990	blood:	n/a
22	chr4:100937264-100937314	NT2-D1	testis:	n/a
23	chr4:100963223-100963273	MCF-7	breast:	n/a
24	chr4:100963223-100963273	HRE	kidney:	n/a
25	chr4:100937264-100937314	SK-N-SH_RA	brain:	n/a
26	chr4:100963223-100963273	HNPCEpiC	eye:	n/a
27	chr4:100963223-100963273	NHDF-neo	bronchial:	n/a
28	chr4:100963223-100963273	BE2_C	brain:	n/a
29	chr4:100937264-100937314	HCF	heart:	n/a
30	chr4:100937264-100937314	AG10803	skin:	n/a
31	chr4:100937264-100937314	MCF10A-Er-Src	breast:	n/a
32	chr4:100937264-100937314	AG09309	skin:	n/a
33	chr4:100963223-100963273	ECC-1	luminal epithelium:	n/a
34	chr4:100963223-100963273	Hepatocyte	liver:	n/a
35	chr4:100963223-100963273	U87	brain:	n/a
36	chr4:100937264-100937314	AoSMC	blood vessel:	n/a
37	chr4:100963223-100963273	T-47D	breast:	n/a
38	chr4:100937264-100937314	H1-hESC	embryonic stem cell:	embryo
39	chr4:100963223-100963273	NHBE	bronchial:	n/a
40	chr4:100963223-100963273	Hela-S3	cervix:	n/a
41	chr4:100937264-100937314	ProgFib	skin:	n/a
42	chr4:100963223-100963273	GM12878	blood:	n/a
43	chr4:100937264-100937314	SAEC	small airway:	n/a
44	chr4:100963223-100963273	HEK293	kidney:	embryo
45	chr4:100937264-100937314	U87	brain:	n/a
46	chr4:100963223-100963273	PFSK-1	brain:	n/a
47	chr4:100963223-100963273	H1-hESC	embryonic stem cell:	embryo
48	chr4:100963223-100963273	SKMC	muscle:	n/a
49	chr4:100937264-100937314	HCPEpiC	choroid plexus:	n/a
50	chr4:100937264-100937314	AG04449	skin:	fetal

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:100932443..100934795-chr4:100942614..100944305,2	K562	blood:
2	chr4:100933295..100935388-chr4:100941563..100944305,2	K562	blood:
3	chr4:100939833..100941556-chr4:100947231..100948820,2	MCF-7	breast:
4	chr4:100933295..100935388-chr4:100941563..100944305,2	K562	blood:
5	chr4:100939853..100942918-chr4:100944283..100946083,3	K562	blood:
6	chr4:100932443..100934795-chr4:100942614..100944305,2	K562	blood:
7	chr4:100910888..100913568-chr4:100928620..100930251,2	MCF-7	breast:
8	chr4:100939833..100941556-chr4:100947231..100948820,2	MCF-7	breast:
9	chr4:100871193..100872810-chr4:100932962..100935747,2	K562	blood:
10	chr4:100869883..100872810-chr4:100932962..100936343,3	K562	blood:
11	chr4:100869793..100871420-chr4:100936616..100939026,2	K562	blood:
12	chr4:100939853..100942918-chr4:100944283..100946083,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAPP1-2	chr4:100955091-100955177	ENSG00000245322.2
2	lnc-DAPP1-2	chr4:100946096-100946237	ENSG00000245322.2
3	lnc-H2AFZ-3	chr4:100962998-100963261	NONHSAT097554
4	lnc-DAPP1-2	chr4:100929228-100929388	ENSG00000245322.2
5	lnc-DAPP1-2	chr4:100955091-100955177	ENSG00000245322.2
6	lnc-DAPP1-2	chr4:100958685-100958862	ENSG00000245322.2
7	lnc-DAPP1-2	chr4:100946439-100946484	ENSG00000245322.2
8	lnc-DAPP1-2	chr4:100958685-100958799	ENSG00000245322.2
9	lnc-DAPP1-2	chr4:100946439-100946484	ENSG00000245322.2
10	lnc-DAPP1-2	chr4:100929059-100929388	ENSG00000245322.2
11	lnc-DAPP1-2	chr4:100958685-100958977	ENSG00000245322.2
12	lnc-DAPP1-2	chr4:100955091-100955177	ENSG00000245322.2
13	lnc-DAPP1-2	chr4:100946439-100946484	ENSG00000245322.2

No data

Variant related genes	Relation type
ENSG00000245322	TF binding region
ENSG00000248820	TF binding region
ENSG00000245322	CpG island
ENSG00000248820	CpG island
ENSG00000245322	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000250403	chromatin interactions

Extended variants
information (count: 695 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543088883	chr4:100928009-100928010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563403571	chr4:100928045-100928046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142286306	chr4:100928070-100928071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191739104	chr4:100928073-100928074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184564181	chr4:100928082-100928083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188880133	chr4:100928153-100928154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370493961	chr4:100928170-100928171	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs374610901	chr4:100928239-100928240	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs543915230	chr4:100928264-100928265	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs547893264	chr4:100928279-100928280	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs115537151	chr4:100928324-100928325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79911559	chr4:100928345-100928346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76333994	chr4:100928355-100928356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182476490	chr4:100928361-100928362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4320141	chr4:100928399-100928400	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs548609937	chr4:100928623-100928624	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs62306097	chr4:100928624-100928625	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567160296	chr4:100928708-100928709	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs56007968	chr4:100928764-100928765	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs556594339	chr4:100928767-100928768	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541457179	chr4:100928822-100928823	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559849992	chr4:100928885-100928886	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs533474544	chr4:100928931-100928932	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs80085747	chr4:100928976-100928977	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570227991	chr4:100929018-100929019	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201256061	chr4:100929028-100929029	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531046923	chr4:100929176-100929177	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs373959641	chr4:100929193-100929194	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs190575981	chr4:100929197-100929198	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs549630237	chr4:100929208-100929209	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs35044019	chr4:100929237-100929238	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs532849134	chr4:100929267-100929268	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs567641299	chr4:100929271-100929272	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs150645792	chr4:100929282-100929283	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs139679337	chr4:100929301-100929302	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs570965697	chr4:100929310-100929311	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs149766625	chr4:100929317-100929318	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs538726701	chr4:100929344-100929345	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs368788652	chr4:100929346-100929347	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs556822763	chr4:100929498-100929499	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575377311	chr4:100929510-100929511	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542482653	chr4:100929511-100929512	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs180986048	chr4:100929519-100929520	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28483464	chr4:100929521-100929522	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs541395617	chr4:100929592-100929593	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs117212760	chr4:100929617-100929618	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147886562	chr4:100929625-100929626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs2015331	chr4:100929666-100929667	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141430121	chr4:100929713-100929714	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539262859	chr4:100929793-100929794	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	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
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100927600-100928400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr4:100928800-100929200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:100929000-100929600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr4:100929000-100930000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr4:100929000-100930000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:100929000-100930000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:100929000-100930000	Enhancers	NHEK	skin
8	chr4:100929200-100930000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:100929200-100930000	Enhancers	HSMM	muscle
10	chr4:100929200-100930600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:100929200-100930800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:100929400-100929800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:100930000-100930800	Weak transcription	HSMM	muscle
14	chr4:100930000-100939400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:100930600-100930800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:100930800-100931000	Enhancers	HSMM	muscle
17	chr4:100935600-100939000	Weak transcription	A549	lung
18	chr4:100936400-100938000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:100937200-100937800	Enhancers	NHLF	lung
20	chr4:100938000-100939000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:100938600-100939800	Enhancers	NHEK	skin
22	chr4:100938800-100939800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:100938800-100939800	Enhancers	HMEC	breast
24	chr4:100939000-100939200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr4:100939000-100939800	Enhancers	A549	lung
26	chr4:100939200-100939800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr4:100939400-100939800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:100942600-100943600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:100943000-100946000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr4:100943200-100945400	Enhancers	Fetal Heart	heart
31	chr4:100943400-100944200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:100943400-100944600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:100943400-100944600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:100943600-100944000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:100943600-100944200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:100943600-100944600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr4:100943800-100944200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:100943800-100944200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr4:100943800-100944200	Active TSS	Stomach Smooth Muscle	stomach
40	chr4:100943800-100944400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:100943800-100944400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr4:100943800-100944600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr4:100943800-100944600	Enhancers	Colon Smooth Muscle	Colon
44	chr4:100943800-100944800	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr4:100944000-100944400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr4:100944000-100944600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr4:100944000-100944600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr4:100944000-100944600	Enhancers	Brain Germinal Matrix	brain
49	chr4:100944000-100944600	Enhancers	Fetal Stomach	stomach
50	chr4:100944000-100945800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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