Variant report

Variant	nsv461631
Chromosome Location	chr4:119261939-119308603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:854)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:119273220-119273579	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:119274135-119274146	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr4:119273963-119274383	GM12878	blood:	n/a	chr4:119274073-119274086 chr4:119274079-119274092
4	BHLHE40	chr4:119274055-119274318	K562	blood:	n/a	chr4:119274073-119274089 chr4:119274300-119274316 chr4:119274075-119274091
5	BHLHE40	chr4:119274053-119274379	HepG2	liver:	n/a	chr4:119274308-119274324 chr4:119274073-119274089 chr4:119274300-119274316 chr4:119274075-119274091
6	BHLHE40	chr4:119274124-119274292	A549	lung:	n/a	n/a
7	BHLHE40	chr4:119274032-119274393	GM12878	blood:	n/a	chr4:119274308-119274324 chr4:119274073-119274089 chr4:119274300-119274316 chr4:119274075-119274091
8	BHLHE40	chr4:119274138-119274294	HepG2	liver:	n/a	n/a
9	BRCA1	chr4:119273423-119273462	HepG2	liver:	n/a	n/a
10	BRCA1	chr4:119262898-119262947	GM12878	blood:	n/a	n/a
11	BRCA1	chr4:119274099-119274232	H1-hESC	embryonic stem cell:	n/a	n/a
12	CCNT2	chr4:119274018-119274408	K562	blood:	n/a	n/a
13	CEBPB	chr4:119274097-119274344	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr4:119265948-119266441	HCT-116	colon:	n/a	n/a
15	CEBPB	chr4:119281401-119281624	A549	lung:	n/a	chr4:119281590-119281598 chr4:119281492-119281503
16	CEBPB	chr4:119277947-119278246	IMR90	lung:	n/a	chr4:119277970-119277981
17	CEBPB	chr4:119288580-119288812	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:119281330-119281636	IMR90	lung:	n/a	chr4:119281590-119281598 chr4:119281492-119281503
19	CEBPB	chr4:119294969-119295325	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:119293193-119293304	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:119272368-119272493	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:119274041-119274247	Hela-S3	cervix:	n/a	chr4:119274085-119274098
23	CHD1	chr4:119274185-119274208	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr4:119274142-119274306	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr4:119274090-119274333	Hela-S3	cervix:	n/a	n/a
26	CREB1	chr4:119274043-119274406	A549	lung:	n/a	n/a
27	CTBP2	chr4:119274019-119274543	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr4:119274120-119274270	AG04450	lung:	n/a	n/a
29	CTCF	chr4:119273300-119273450	HMEC	breast:	n/a	n/a
30	CTCF	chr4:119274140-119274290	HL-60	blood:	n/a	n/a
31	CTCF	chr4:119274120-119274270	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr4:119274540-119274690	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr4:119274140-119274290	GM12871	blood:	n/a	n/a
34	CTCF	chr4:119273300-119273450	HRE	kidney:	n/a	n/a
35	CTCF	chr4:119279600-119279750	HEEpiC	esophagus:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
36	CTCF	chr4:119274140-119274290	GM06990	blood:	n/a	n/a
37	CTCF	chr4:119279460-119279610	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr4:119279532-119279811	H1-hESC	embryonic stem cell:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
39	CTCF	chr4:119279660-119279810	HCPEpiC	choroid plexus:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
40	CTCF	chr4:119288458-119288510	GM10266	blood:	n/a	n/a
41	CTCF	chr4:119274140-119274290	RPTEC	kidney:	n/a	n/a
42	CTCF	chr4:119273426-119273504	NHEK	skin:	n/a	n/a
43	CTCF	chr4:119273864-119274384	K562	blood:	n/a	chr4:119274068-119274077 chr4:119274304-119274317 chr4:119274062-119274080 chr4:119274029-119274042 chr4:119273979-119273992 chr4:119274112-119274125
44	CTCF	chr4:119274441-119274523	GM13977	blood:	n/a	n/a
45	CTCF	chr4:119274140-119274290	GM12878	blood:	n/a	n/a
46	CTCF	chr4:119279580-119279730	K562	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
47	CTCF	chr4:119274608-119274612	GM10248	blood:	n/a	n/a
48	CTCF	chr4:119274634-119274647	GM10266	blood:	n/a	n/a
49	CTCF	chr4:119274110-119274322	HUVEC	blood vessel:	n/a	chr4:119274304-119274317 chr4:119274112-119274125
50	CTCF	chr4:119274160-119274310	GM12870	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119295633-119295683	LNCaP	prostate:	n/a
2	chr4:119273827-119273877	GM12878	blood:	n/a
3	chr4:119273889-119273939	AG09309	skin:	n/a
4	chr4:119273073-119273123	HCPEpiC	choroid plexus:	n/a
5	chr4:119274341-119274391	SKMC	muscle:	n/a
6	chr4:119274837-119274887	HUVEC	blood vessel:	n/a
7	chr4:119274192-119274242	GM12892	blood:	n/a
8	chr4:119274341-119274391	AG04449	skin:	fetal
9	chr4:119273361-119273411	SAEC	small airway:	n/a
10	chr4:119274837-119274887	LNCaP	prostate:	n/a
11	chr4:119273073-119273123	SK-N-SH_RA	brain:	n/a
12	chr4:119282020-119282070	BJ	skin:	n/a
13	chr4:119282020-119282070	HEEpiC	esophagus:	n/a
14	chr4:119274837-119274887	NH-A	brain:	n/a
15	chr4:119273827-119273877	PFSK-1	brain:	n/a
16	chr4:119274013-119274063	PFSK-1	brain:	n/a
17	chr4:119273073-119273123	HUVEC	blood vessel:	n/a
18	chr4:119274013-119274063	A549	lung:	n/a
19	chr4:119273827-119273877	CMK	blood:	n/a
20	chr4:119270205-119270255	HUVEC	blood vessel:	n/a
21	chr4:119273889-119273939	AG04450	lung:	fetal
22	chr4:119274133-119274183	NT2-D1	testis:	n/a
23	chr4:119282020-119282070	ProgFib	skin:	n/a
24	chr4:119274837-119274887	HCF	heart:	n/a
25	chr4:119284446-119284496	HIPEpiC	eye:	n/a
26	chr4:119284446-119284496	NHBE	bronchial:	n/a
27	chr4:119273889-119273939	HEEpiC	esophagus:	n/a
28	chr4:119270205-119270255	ECC-1	luminal epithelium:	n/a
29	chr4:119274192-119274242	Hepatocyte	liver:	n/a
30	chr4:119274133-119274183	Hela-S3	cervix:	n/a
31	chr4:119274837-119274887	U87	brain:	n/a
32	chr4:119274133-119274183	AG04450	lung:	fetal
33	chr4:119295633-119295683	A549	lung:	n/a
34	chr4:119295633-119295683	SK-N-SH	brain:	n/a
35	chr4:119273827-119273877	Hela-S3	cervix:	n/a
36	chr4:119273827-119273877	BJ	skin:	n/a
37	chr4:119273889-119273939	Hela-S3	cervix:	n/a
38	chr4:119284446-119284496	IMR90	lung:	fetal
39	chr4:119274192-119274242	PFSK-1	brain:	n/a
40	chr4:119274133-119274183	PFSK-1	brain:	n/a
41	chr4:119273073-119273123	HRPEpiC	eye:	n/a
42	chr4:119274837-119274887	SK-N-SH_RA	brain:	n/a
43	chr4:119273361-119273411	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:119273361-119273411	HepG2	liver:	n/a
45	chr4:119276652-119276702	U87	brain:	n/a
46	chr4:119274013-119274063	NT2-D1	testis:	n/a
47	chr4:119270205-119270255	Caco-2	colon:	n/a
48	chr4:119274013-119274063	ProgFib	skin:	n/a
49	chr4:119274837-119274887	Hepatocyte	liver:	n/a
50	chr4:119273827-119273877	BE2_C	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:119200018..119201698-chr4:119270119..119271961,2	MCF-7	breast:
2	chr4:119200552..119202977-chr4:119264974..119267166,2	MCF-7	breast:
3	chr4:119297227..119299368-chr4:119300296..119302370,2	K562	blood:
4	chr4:119199692..119204423-chr4:119272219..119275323,9	MCF-7	breast:
5	chr4:119202174..119205868-chr4:119258505..119262976,4	MCF-7	breast:
6	chr4:119292842..119294538-chr4:119297260..119300160,2	MCF-7	breast:
7	chr4:119292842..119294538-chr4:119297260..119300160,2	MCF-7	breast:
8	chr4:119265038..119266612-chr4:119268208..119270240,2	K562	blood:
9	chr4:119202015..119204587-chr4:119283908..119285983,2	K562	blood:
10	chr4:119202395..119204664-chr4:119270444..119272210,2	MCF-7	breast:
11	chr4:119199765..119204001-chr4:119271592..119273818,4	K562	blood:
12	chr4:119297227..119299368-chr4:119300296..119302370,2	K562	blood:
13	chr4:119204030..119205775-chr4:119295374..119296879,2	K562	blood:
14	chr4:119199853..119201646-chr4:119293860..119297820,3	MCF-7	breast:
15	chr4:119265038..119266612-chr4:119268208..119270240,2	K562	blood:
16	chr4:119198677..119205956-chr4:119272273..119279963,18	MCF-7	breast:
17	chr4:119208423..119210382-chr4:119267375..119269771,2	MCF-7	breast:
18	chr4:119201789..119203327-chr4:119280623..119282185,2	K562	blood:
19	chr4:119199772..119201389-chr4:119276128..119279305,3	MCF-7	breast:

No data

Variant related genes	Relation type
PRSS12	TF binding region
PRSS12	CpG island
ENSG00000269893	chromatin interactions

Extended variants
information (count: 1124 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs788656	chr4:119261939-119261940	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146873074	chr4:119261944-119261945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182534101	chr4:119261950-119261951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562791971	chr4:119261983-119261984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531852664	chr4:119261986-119261987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139773122	chr4:119261987-119261988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78959044	chr4:119261988-119261989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527990581	chr4:119261989-119261990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548151289	chr4:119262103-119262104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567971482	chr4:119262130-119262131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530272108	chr4:119262215-119262216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187269573	chr4:119262221-119262222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564378686	chr4:119262247-119262248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192152010	chr4:119262272-119262273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371048190	chr4:119262314-119262315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79067277	chr4:119262366-119262367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557445814	chr4:119262412-119262413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369880252	chr4:119262520-119262521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183982272	chr4:119262579-119262580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1916687	chr4:119262604-119262605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188877712	chr4:119262607-119262608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553609521	chr4:119262631-119262632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573599287	chr4:119262683-119262684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542427302	chr4:119262690-119262691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192713545	chr4:119262745-119262746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530095691	chr4:119262762-119262763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184525120	chr4:119262777-119262778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187910704	chr4:119262779-119262780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572432471	chr4:119262785-119262786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541442760	chr4:119262787-119262788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561537782	chr4:119262800-119262801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530433265	chr4:119262834-119262835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551670505	chr4:119262853-119262854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115455238	chr4:119262956-119262957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563936776	chr4:119262962-119262963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531303351	chr4:119263045-119263046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559365639	chr4:119263065-119263066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76318312	chr4:119263079-119263080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371979222	chr4:119263091-119263092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533498189	chr4:119263117-119263118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146558558	chr4:119263208-119263209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567185629	chr4:119263257-119263258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113312974	chr4:119263300-119263301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78190723	chr4:119263304-119263305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556061810	chr4:119263319-119263320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576230450	chr4:119263339-119263340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538466701	chr4:119263349-119263350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559049820	chr4:119263356-119263357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141240147	chr4:119263362-119263363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572594315	chr4:119263395-119263396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119202800-119267200	Weak transcription	Stomach Mucosa	stomach
2	chr4:119229000-119267200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:119253000-119262200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:119256800-119262000	Enhancers	NHDF-Ad	bronchial
5	chr4:119258600-119262000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:119258600-119262000	Enhancers	HMEC	breast
7	chr4:119258600-119262200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr4:119259000-119262000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:119259200-119262000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:119259200-119262200	Enhancers	NHEK	skin
11	chr4:119259400-119267000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:119259600-119267800	Weak transcription	Fetal Brain Male	brain
13	chr4:119260400-119264400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr4:119260600-119262000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:119260600-119262000	Enhancers	Muscle Satellite Cultured Cells	--
16	chr4:119260800-119262000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:119261000-119262000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:119261200-119262000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:119261200-119262200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:119261200-119262200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:119261200-119262400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:119261200-119263400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr4:119261200-119266000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr4:119261400-119262400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:119261600-119265600	Weak transcription	Brain Germinal Matrix	brain
26	chr4:119261600-119266000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:119261600-119272200	Weak transcription	Fetal Brain Female	brain
28	chr4:119261800-119262200	Weak transcription	NHLF	lung
29	chr4:119261800-119265400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:119261800-119266000	Weak transcription	Osteobl	bone
31	chr4:119261800-119267000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr4:119262000-119264600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr4:119262000-119265800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:119262000-119266000	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr4:119262000-119266000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:119262000-119266000	Weak transcription	NHDF-Ad	bronchial
37	chr4:119262000-119266200	Weak transcription	HMEC	breast
38	chr4:119262000-119267000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr4:119262000-119267000	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr4:119262000-119267000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:119262200-119262400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:119262200-119262400	Enhancers	NHLF	lung
43	chr4:119262200-119266000	Weak transcription	NHEK	skin
44	chr4:119262200-119266600	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr4:119262200-119267000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr4:119262200-119267200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:119262400-119264200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr4:119262400-119266000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr4:119262400-119267000	Weak transcription	NHLF	lung
50	chr4:119262400-119268800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links