Variant report

Variant	nsv878736
Chromosome Location	chr4:20233035-20279858
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:20249744-20250041	HepG2	liver:	n/a	n/a
2	ATF1	chr4:20266308-20266378	K562	blood:	n/a	n/a
3	BACH1	chr4:20258084-20258289	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:20254954-20255182	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:20256465-20257405	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:20254170-20254488	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:20253093-20253368	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr4:20253739-20253744	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:20256675-20257000	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:20249676-20250155	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:20233802-20234105	IMR90	lung:	n/a	chr4:20233976-20233987
12	CEBPB	chr4:20249658-20250111	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:20233929-20233997	HepG2	liver:	n/a	chr4:20233976-20233987
14	CEBPB	chr4:20253475-20253672	Hela-S3	cervix:	n/a	n/a
15	CHD1	chr4:20253777-20253954	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr4:20254101-20254405	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr4:20253545-20253717	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr4:20252935-20253747	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr4:20253125-20253331	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:20256508-20256847	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr4:20252818-20254039	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr4:20254251-20256981	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr4:20249797-20250057	Spleen_OC	spleen:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
24	CTCF	chr4:20254000-20254150	SAEC	small airway:	n/a	chr4:20254078-20254091
25	CTCF	chr4:20250280-20250430	HEK293	kidney:	n/a	n/a
26	CTCF	chr4:20249860-20250010	HUVEC	blood vessel:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
27	CTCF	chr4:20249840-20249990	MCF-7	breast:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
28	CTCF	chr4:20251100-20251250	NHLF	lung:	n/a	n/a
29	CTCF	chr4:20249780-20249930	HAc	cerebellar:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
30	CTCF	chr4:20250120-20250270	GM12878	blood:	n/a	n/a
31	CTCF	chr4:20256680-20256830	HUVEC	blood vessel:	n/a	chr4:20256759-20256772
32	CTCF	chr4:20254048-20254097	MCF-7	breast:	n/a	chr4:20254078-20254091
33	CTCF	chr4:20249800-20249950	Hela-S3	cervix:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
34	CTCF	chr4:20250180-20250330	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr4:20251100-20251250	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr4:20249840-20249990	HL-60	blood:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
37	CTCF	chr4:20249790-20250018	Lung_OC	lung:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
38	CTCF	chr4:20251196-20251367	K562	blood:	n/a	n/a
39	CTCF	chr4:20249764-20250032	HepG2	liver:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
40	CTCF	chr4:20249780-20249930	A549	lung:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
41	CTCF	chr4:20249840-20249990	HCPEpiC	choroid plexus:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
42	CTCF	chr4:20251140-20251290	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr4:20249840-20249990	GM12867	blood:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
44	CTCF	chr4:20249790-20250034	Hela-S3	cervix:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
45	CTCF	chr4:20253340-20253490	AG04449	skin:	n/a	chr4:20253440-20253450
46	CTCF	chr4:20250130-20250154	GM20000	blood:	n/a	n/a
47	CTCF	chr4:20251140-20251290	AG09309	skin:	n/a	n/a
48	CTCF	chr4:20249860-20250010	BE2_C	brain:	n/a	chr4:20249901-20249919 chr4:20249896-20249917 chr4:20249903-20249916 chr4:20249902-20249918
49	CTCF	chr4:20250220-20250370	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr4:20254060-20254210	HUVEC	blood vessel:	n/a	chr4:20254078-20254091

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20255805-20255855	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:20255805-20255855	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:20254736-20254786	PFSK-1	brain:	n/a
4	chr4:20259899-20259949	SK-N-SH	brain:	n/a
5	chr4:20259899-20259949	HRPEpiC	eye:	n/a
6	chr4:20255061-20255111	HMEC	breast:	n/a
7	chr4:20256841-20256891	SK-N-SH	brain:	n/a
8	chr4:20256841-20256891	GM06990	blood:	n/a
9	chr4:20257590-20257640	AG10803	skin:	n/a
10	chr4:20255264-20255314	AG09319	gingival:	n/a
11	chr4:20255187-20255237	RPTEC	kidney:	n/a
12	chr4:20253514-20253564	BE2_C	brain:	n/a
13	chr4:20253277-20253327	Caco-2	colon:	n/a
14	chr4:20253556-20253606	GM12891	blood:	n/a
15	chr4:20253277-20253327	SK-N-SH_RA	brain:	n/a
16	chr4:20253922-20253972	MCF10A-Er-Src	breast:	n/a
17	chr4:20255343-20255393	GM06990	blood:	n/a
18	chr4:20255082-20255132	HEEpiC	esophagus:	n/a
19	chr4:20254519-20254569	SK-N-SH	brain:	n/a
20	chr4:20253130-20253180	K562	blood:	n/a
21	chr4:20254519-20254569	HCT-116	colon:	n/a
22	chr4:20256841-20256891	HCT-116	colon:	n/a
23	chr4:20253130-20253180	HUVEC	blood vessel:	n/a
24	chr4:20259899-20259949	AG09309	skin:	n/a
25	chr4:20254519-20254569	AG09319	gingival:	n/a
26	chr4:20253922-20253972	MCF-7	breast:	n/a
27	chr4:20254736-20254786	SK-N-SH	brain:	n/a
28	chr4:20253595-20253645	MCF10A-Er-Src	breast:	n/a
29	chr4:20255082-20255132	AG09319	gingival:	n/a
30	chr4:20253514-20253564	PANC-1	pancreas:	n/a
31	chr4:20257590-20257640	AG09319	gingival:	n/a
32	chr4:20255061-20255111	HIPEpiC	eye:	n/a
33	chr4:20256841-20256891	AG09309	skin:	n/a
34	chr4:20253922-20253972	HCPEpiC	choroid plexus:	n/a
35	chr4:20254140-20254190	SK-N-SH_RA	brain:	n/a
36	chr4:20256326-20256376	A549	lung:	n/a
37	chr4:20255082-20255132	MCF-7	breast:	n/a
38	chr4:20255082-20255132	AG10803	skin:	n/a
39	chr4:20253130-20253180	AG09309	skin:	n/a
40	chr4:20254140-20254190	PANC-1	pancreas:	n/a
41	chr4:20253595-20253645	GM06990	blood:	n/a
42	chr4:20255805-20255855	HRPEpiC	eye:	n/a
43	chr4:20253130-20253180	HCT-116	colon:	n/a
44	chr4:20254140-20254190	SK-N-MC	brain:	n/a
45	chr4:20255187-20255237	HRCEpiC	kidney:	n/a
46	chr4:20255082-20255132	HCM	heart:	n/a
47	chr4:20255985-20256035	NH-A	brain:	n/a
48	chr4:20255805-20255855	NH-A	brain:	n/a
49	chr4:20256326-20256376	BJ	skin:	n/a
50	chr4:20255805-20255855	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20252458..20255013-chr4:20255238..20258452,3	MCF-7	breast:
2	chr4:20264521..20266805-chr4:20268448..20270041,2	K562	blood:
3	chr4:20274898..20276936-chr4:20279121..20281549,2	MCF-7	breast:
4	chr4:20252097..20254985-chr4:20256141..20260392,5	MCF-7	breast:
5	chr4:20254313..20256018-chr4:20262688..20264505,2	MCF-7	breast:
6	chr4:20271116..20273425-chr4:20275227..20278137,2	K562	blood:
7	chr4:20025908..20028659-chr4:20253195..20254796,2	MCF-7	breast:
8	chr4:20240508..20242513-chr4:20257215..20258774,2	K562	blood:
9	chr4:20274898..20276936-chr4:20279121..20281549,2	MCF-7	breast:
10	chr4:19310675..19311570-chr4:20249856..20250798,3	MCF-7	breast:
11	chr4:20252458..20255013-chr4:20255238..20258452,3	MCF-7	breast:
12	chr4:20252097..20254985-chr4:20256141..20260392,5	MCF-7	breast:
13	chr4:20264521..20266805-chr4:20268448..20270041,2	K562	blood:
14	chr4:20271116..20273425-chr4:20275227..20278137,2	K562	blood:
15	chr4:20235739..20237301-chr4:20237746..20240532,2	MCF-7	breast:
16	chr4:20240508..20242513-chr4:20257215..20258774,2	K562	blood:
17	chr4:20235739..20237301-chr4:20237746..20240532,2	MCF-7	breast:
18	chr4:20247665..20250072-chr4:20255002..20257990,2	MCF-7	breast:

Variant related genes	Relation type
SLIT2	TF binding region
SLIT2	CpG island
ENSG00000145147	chromatin interactions

Extended variants
information (count: 1266 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565933632	chr4:20239200-20239201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187807220	chr4:20239209-20239210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542105980	chr4:20239242-20239243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576757638	chr4:20239293-20239294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142313874	chr4:20239308-20239309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569516738	chr4:20239324-20239325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150505121	chr4:20239347-20239348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555034092	chr4:20239355-20239356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192286522	chr4:20239370-20239371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552830367	chr4:20239522-20239523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539706477	chr4:20239535-20239536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552710611	chr4:20239596-20239597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578167545	chr4:20239605-20239606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552960149	chr4:20239658-20239659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28608644	chr4:20239663-20239664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs35175721	chr4:20239715-20239716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs56356936	chr4:20239724-20239725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543280048	chr4:20239736-20239737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77493469	chr4:20239746-20239747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374154412	chr4:20239792-20239793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528597122	chr4:20239795-20239796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184487489	chr4:20239822-20239823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565143275	chr4:20239823-20239824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533011213	chr4:20239863-20239864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551258418	chr4:20239875-20239876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369137411	chr4:20239975-20239976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569656396	chr4:20240022-20240023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539836618	chr4:20240044-20240045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370975674	chr4:20240047-20240048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs80147640	chr4:20240093-20240094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111879218	chr4:20240118-20240119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111373502	chr4:20240152-20240153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541611810	chr4:20240157-20240158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571154438	chr4:20240163-20240164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188854958	chr4:20240171-20240172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192708418	chr4:20240182-20240183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35757422	chr4:20240220-20240221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142487450	chr4:20240221-20240222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576038014	chr4:20240222-20240223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575797165	chr4:20240237-20240238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs71653871	chr4:20240241-20240242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs34624560	chr4:20240243-20240244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200315166	chr4:20240244-20240245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35273775	chr4:20240257-20240258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144516431	chr4:20240265-20240266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554877880	chr4:20240321-20240322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546281424	chr4:20240328-20240329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573246466	chr4:20240329-20240330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139624157	chr4:20240347-20240348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79688719	chr4:20240358-20240359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Cancer	20164919	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20239200-20240000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:20239200-20240400	Enhancers	NHEK	skin
3	chr4:20240000-20240600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:20240600-20240800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:20247600-20248000	Enhancers	Fetal Lung	lung
6	chr4:20248000-20252200	Weak transcription	Fetal Lung	lung
7	chr4:20248400-20248600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:20248600-20249600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:20248800-20250400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:20248800-20251200	Enhancers	NHDF-Ad	bronchial
11	chr4:20249000-20252600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:20249200-20250600	Enhancers	NHLF	lung
13	chr4:20249200-20250600	Enhancers	Osteobl	bone
14	chr4:20249600-20250000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:20249800-20250200	Enhancers	NHEK	skin
16	chr4:20249800-20250400	Enhancers	Rectal Smooth Muscle	rectum
17	chr4:20250000-20250200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:20250000-20250200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:20250000-20250200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:20250000-20250200	Enhancers	Brain Hippocampus Middle	brain
21	chr4:20250000-20250200	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr4:20250000-20250200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr4:20250000-20250200	Enhancers	HUVEC	blood vessel
24	chr4:20250000-20250400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr4:20250000-20250400	Enhancers	Hela-S3	cervix
26	chr4:20250000-20250600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr4:20250000-20250800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:20250000-20252200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:20250200-20250400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
30	chr4:20250200-20250400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr4:20250200-20250400	Enhancers	Fetal Muscle Leg	muscle
32	chr4:20250200-20250400	Enhancers	Fetal Stomach	stomach
33	chr4:20250200-20250400	Enhancers	Spleen	Spleen
34	chr4:20250200-20250600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:20250200-20250600	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr4:20250200-20252600	Weak transcription	Brain Hippocampus Middle	brain
37	chr4:20250200-20252800	Weak transcription	HUVEC	blood vessel
38	chr4:20250200-20252800	Weak transcription	NHEK	skin
39	chr4:20250400-20252600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr4:20250400-20252600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr4:20250400-20252800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:20250400-20252800	Weak transcription	Rectal Smooth Muscle	rectum
43	chr4:20250400-20252800	Weak transcription	Hela-S3	cervix
44	chr4:20250600-20251000	Weak transcription	Osteobl	bone
45	chr4:20250600-20252000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:20250600-20252600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:20250600-20252800	Weak transcription	NHLF	lung
48	chr4:20250800-20251200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr4:20251000-20252600	Enhancers	Osteobl	bone
50	chr4:20251200-20251400	Enhancers	Muscle Satellite Cultured Cells	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links