Variant report

Variant	esv3407256
Chromosome Location	chrX:31214281-31548379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2545)
CpG islands
(count:1098)
Chromatin interactive
region (count:17)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2545 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31239155-31239996	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:31374459-31375489	HepG2	liver:	n/a	chrX:31374966-31374982
3	ARID3A	chrX:31441684-31441786	K562	blood:	n/a	n/a
4	ARID3A	chrX:31283251-31283891	HepG2	liver:	n/a	n/a
5	ARID3A	chrX:31284124-31284273	HepG2	liver:	n/a	n/a
6	ARID3A	chrX:31442158-31442355	HepG2	liver:	n/a	n/a
7	ARID3A	chrX:31368398-31368911	HepG2	liver:	n/a	n/a
8	ARID3A	chrX:31292505-31292520	K562	blood:	n/a	n/a
9	ATF1	chrX:31341826-31342081	K562	blood:	n/a	n/a
10	ATF1	chrX:31242002-31242188	K562	blood:	n/a	n/a
11	ATF1	chrX:31390110-31390428	K562	blood:	n/a	n/a
12	ATF1	chrX:31299839-31299907	K562	blood:	n/a	n/a
13	ATF1	chrX:31312610-31312891	K562	blood:	n/a	n/a
14	ATF2	chrX:31246941-31247439	GM12878	blood:	n/a	n/a
15	ATF2	chrX:31254359-31254700	GM12878	blood:	n/a	n/a
16	ATF2	chrX:31254270-31254784	GM12878	blood:	n/a	n/a
17	ATF2	chrX:31246878-31247438	GM12878	blood:	n/a	n/a
18	BACH1	chrX:31517260-31517602	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chrX:31284456-31284765	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chrX:31461975-31462162	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chrX:31246482-31246833	GM12878	blood:	n/a	n/a
22	BATF	chrX:31246991-31247341	GM12878	blood:	n/a	n/a
23	BATF	chrX:31290611-31290947	GM12878	blood:	n/a	n/a
24	BATF	chrX:31233511-31233888	GM12878	blood:	n/a	n/a
25	BATF	chrX:31227213-31227448	GM12878	blood:	n/a	n/a
26	BATF	chrX:31233582-31233839	GM12878	blood:	n/a	n/a
27	BATF	chrX:31246962-31247349	GM12878	blood:	n/a	n/a
28	BATF	chrX:31254437-31254684	GM12878	blood:	n/a	n/a
29	BATF	chrX:31242003-31242303	GM12878	blood:	n/a	n/a
30	BCL11A	chrX:31233501-31233837	GM12878	blood:	n/a	n/a
31	BCL11A	chrX:31254396-31254648	GM12878	blood:	n/a	n/a
32	BCL11A	chrX:31247122-31247337	GM12878	blood:	n/a	n/a
33	BCL11A	chrX:31247019-31247398	GM12878	blood:	n/a	n/a
34	BCL11A	chrX:31252024-31252275	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCLAF1	chrX:31241954-31242244	GM12878	blood:	n/a	n/a
36	BCLAF1	chrX:31246965-31247462	GM12878	blood:	n/a	n/a
37	BHLHE40	chrX:31239181-31239900	HepG2	liver:	n/a	n/a
38	BHLHE40	chrX:31341800-31341935	GM12878	blood:	n/a	n/a
39	BHLHE40	chrX:31361626-31361856	HepG2	liver:	n/a	n/a
40	BHLHE40	chrX:31217885-31218273	HepG2	liver:	n/a	n/a
41	BHLHE40	chrX:31254478-31254682	GM12878	blood:	n/a	n/a
42	BHLHE40	chrX:31290652-31290893	GM12878	blood:	n/a	n/a
43	BHLHE40	chrX:31247030-31247436	GM12878	blood:	n/a	n/a
44	BHLHE40	chrX:31361587-31361844	K562	blood:	n/a	n/a
45	BHLHE40	chrX:31258998-31259008	GM12878	blood:	n/a	n/a
46	BHLHE40	chrX:31233514-31233890	GM12878	blood:	n/a	n/a
47	BHLHE40	chrX:31232179-31232413	GM12878	blood:	n/a	n/a
48	BHLHE40	chrX:31255324-31255645	GM12878	blood:	n/a	n/a
49	BRCA1	chrX:31439052-31439392	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chrX:31374799-31375406	Hela-S3	cervix:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31285204-31285254	GM12892	blood:	n/a
2	chrX:31285018-31285068	NH-A	brain:	n/a
3	chrX:31284505-31284555	PANC-1	pancreas:	n/a
4	chrX:31284448-31284498	MCF10A-Er-Src	breast:	n/a
5	chrX:31282451-31282501	AG09309	skin:	n/a
6	chrX:31285029-31285079	NHDF-neo	bronchial:	n/a
7	chrX:31285489-31285539	HUVEC	blood vessel:	n/a
8	chrX:31285204-31285254	HAEpiC	amniotic membrane:	n/a
9	chrX:31285492-31285542	HepG2	liver:	n/a
10	chrX:31283706-31283756	NHDF-neo	bronchial:	n/a
11	chrX:31285105-31285155	NB4	blood:	n/a
12	chrX:31282451-31282501	HCF	heart:	n/a
13	chrX:31284448-31284498	GM06990	blood:	n/a
14	chrX:31285032-31285082	HCM	heart:	n/a
15	chrX:31282451-31282501	GM12892	blood:	n/a
16	chrX:31285032-31285082	HCT-116	colon:	n/a
17	chrX:31285492-31285542	SK-N-SH	brain:	n/a
18	chrX:31285204-31285254	SKMC	muscle:	n/a
19	chrX:31285009-31285059	GM12891	blood:	n/a
20	chrX:31285018-31285068	CMK	blood:	n/a
21	chrX:31284448-31284498	IMR90	lung:	fetal
22	chrX:31285105-31285155	HCM	heart:	n/a
23	chrX:31285105-31285155	SK-N-MC	brain:	n/a
24	chrX:31285009-31285059	T-47D	breast:	n/a
25	chrX:31526531-31526581	HepG2	liver:	n/a
26	chrX:31283706-31283756	IMR90	lung:	fetal
27	chrX:31285492-31285542	HAEpiC	amniotic membrane:	n/a
28	chrX:31285105-31285155	PANC-1	pancreas:	n/a
29	chrX:31285018-31285068	T-47D	breast:	n/a
30	chrX:31285489-31285539	IMR90	lung:	fetal
31	chrX:31285032-31285082	GM12878	blood:	n/a
32	chrX:31526745-31526795	K562	blood:	n/a
33	chrX:31285009-31285059	AoSMC	blood vessel:	n/a
34	chrX:31285029-31285079	MCF-7	breast:	n/a
35	chrX:31283706-31283756	SAEC	small airway:	n/a
36	chrX:31287275-31287325	U87	brain:	n/a
37	chrX:31285032-31285082	AG10803	skin:	n/a
38	chrX:31287275-31287325	NB4	blood:	n/a
39	chrX:31284813-31284863	LNCaP	prostate:	n/a
40	chrX:31285129-31285179	AoSMC	blood vessel:	n/a
41	chrX:31285492-31285542	PANC-1	pancreas:	n/a
42	chrX:31287275-31287325	HMEC	breast:	n/a
43	chrX:31285018-31285068	ovcar-3	ovarian:	n/a
44	chrX:31285501-31285551	HUVEC	blood vessel:	n/a
45	chrX:31284505-31284555	AG10803	skin:	n/a
46	chrX:31526531-31526581	MCF-7	breast:	n/a
47	chrX:31285501-31285551	SK-N-MC	brain:	n/a
48	chrX:31285204-31285254	T-47D	breast:	n/a
49	chrX:31285492-31285542	SK-N-MC	brain:	n/a
50	chrX:31284813-31284863	HEEpiC	esophagus:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31256880..31259581-chrX:31282243..31284046,2	K562	blood:
2	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:
3	chrX:31436407..31439307-chrX:31440950..31442473,2	K562	blood:
4	chrX:31316037..31318700-chrX:31321039..31322657,2	K562	blood:
5	chrX:31436407..31439307-chrX:31440950..31442473,2	K562	blood:
6	chr1:19276032..19276532-chrX:31231954..31232601,2	MCF-7	breast:
7	chrX:31237187..31239126-chrX:31240873..31243255,2	K562	blood:
8	chrX:31055216..31055947-chrX:31311393..31312206,2	MCF-7	breast:
9	chr5:43121100..43121993-chrX:31284323..31285114,2	Hela-S3	cervix:
10	chrX:31231843..31232710-chrX:31311329..31312068,2	MCF-7	breast:
11	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:
12	chrX:31316037..31318700-chrX:31321039..31322657,2	K562	blood:
13	chrX:31237187..31239126-chrX:31240873..31243255,2	K562	blood:
14	chrX:31311122..31313355-chrX:31314263..31316652,2	K562	blood:
15	chrX:31311122..31313355-chrX:31314263..31316652,2	K562	blood:
16	chrX:31256880..31259581-chrX:31282243..31284046,2	K562	blood:
17	chrX:31231843..31232710-chrX:31311329..31312068,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTHL17-1	chrX:31241147-31241238	NONHSAT136581
2	lnc-GK-4	chrX:31341715-31341747	ENSG00000242286.1
3	lnc-GK-4	chrX:31279225-31279846	ENSG00000242286.1
4	lnc-FTHL17-1	chrX:31284928-31285069	NONHSAT136581
5	lnc-FTHL17-1	chrX:31279073-31279133	NONHSAT136581

No data

Variant related genes	Relation type
DMD	TF binding region
RNU6-894P	TF binding region
DMD	CpG island
RNU6-894P	CpG island
ENSG00000172262	chromatin interactions

Extended variants
information (count: 4839 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4839 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183491796	chrX:31214395-31214396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145286517	chrX:31214410-31214411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187776729	chrX:31214412-31214413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376316367	chrX:31214421-31214422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146421468	chrX:31214568-31214569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192521802	chrX:31214626-31214627	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4829212	chrX:31214669-31214670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144680844	chrX:31214673-31214674	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113812862	chrX:31214684-31214685	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182113391	chrX:31214734-31214735	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7057083	chrX:31214798-31214799	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369984907	chrX:31214833-31214834	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7057481	chrX:31214846-31214847	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186938244	chrX:31214879-31214880	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs59602681	chrX:31214967-31214968	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs60540732	chrX:31215185-31215186	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373462360	chrX:31215188-31215189	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6527072	chrX:31215428-31215429	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs191780603	chrX:31215442-31215443	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185007588	chrX:31215540-31215541	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs72129138	chrX:31215559-31215560	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs398122011	chrX:31215560-31215561	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs199682244	chrX:31215562-31215563	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188322450	chrX:31215563-31215564	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs193044447	chrX:31215586-31215587	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147524413	chrX:31215594-31215595	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs80151508	chrX:31215621-31215622	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139885238	chrX:31215644-31215645	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370805237	chrX:31215667-31215668	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6631263	chrX:31215747-31215748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553196059	chrX:31215824-31215825	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185260486	chrX:31216024-31216025	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147279101	chrX:31216055-31216056	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148738670	chrX:31216062-31216063	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs386416846	chrX:31216141-31216142	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375806347	chrX:31216158-31216159	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61065027	chrX:31216163-31216164	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs61342941	chrX:31216167-31216168	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79934213	chrX:31216179-31216180	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142183071	chrX:31216236-31216237	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181904396	chrX:31216313-31216314	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113225759	chrX:31216457-31216458	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183611805	chrX:31216481-31216482	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188261324	chrX:31216575-31216576	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112304052	chrX:31216577-31216578	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181220951	chrX:31216716-31216717	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144150751	chrX:31216836-31216837	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535016230	chrX:31216902-31216903	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs5926991	chrX:31217022-31217023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140816299	chrX:31217069-31217070	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Cancer	16751803	CNVD
Intellectual disability	23615299	CNVD
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Cancer	20164919	CNVD
Premature ovarian failure	20952765	CNVD
Ovarian cancer	19835627	CNVD
Cerebellar hypoplasia	21569638	CNVD
X-linked lissencephaly	21569638	CNVD
Thyroid cancer	19087340	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17406619	CNVD
Disorders of sex development	22290220	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Gastric adenocarcinoma	19115996	CNVD
Duchenne-like muscular dystrophy	22470819	CNVD
Muscular dystrophy	22470819	CNVD
Pancreatic cancer	17952125	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Duchenne and Becker muscular dystrophies	18663755	CNVD
Gastric cancer	17229543	CNVD
Type 2 diabetes	21760887	CNVD
Cardiomyopathy	22138850	CNVD
Muscular dystrophy	21149563	CNVD
Skeletal myopathy	22138850	CNVD
Autism	21484199	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Duchenne-like muscular dystrophy	22138850	CNVD
Muscular dystrophy	22138850	CNVD
Disease	22090376	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD
Ornithine transcarbamylase deficiency	21467225	CNVD
Myxofibrosarcoma	16751306	CNVD

Chromatin state (count:1636 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31140200-31227600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chrX:31142000-31236600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chrX:31156800-31224800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chrX:31182000-31227000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chrX:31186800-31217600	Weak transcription	Fetal Intestine Small	intestine
6	chrX:31196600-31227600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chrX:31197200-31217400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chrX:31197800-31219400	Weak transcription	Adipose Nuclei	Adipose
9	chrX:31198400-31217200	Weak transcription	HepG2	liver
10	chrX:31201000-31214600	Weak transcription	Pancreas	Pancrea
11	chrX:31201000-31218600	Weak transcription	Left Ventricle	heart
12	chrX:31204400-31216200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chrX:31204400-31231600	Weak transcription	Colon Smooth Muscle	Colon
14	chrX:31205600-31231200	Weak transcription	HSMMtube	muscle
15	chrX:31206800-31219600	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chrX:31206800-31227000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chrX:31208800-31226800	Weak transcription	NH-A	brain
18	chrX:31209000-31217200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chrX:31209800-31217400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chrX:31209800-31219200	Weak transcription	Ovary	ovary
21	chrX:31211400-31217800	Weak transcription	Fetal Heart	heart
22	chrX:31212000-31217800	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chrX:31212600-31231600	Weak transcription	Stomach Smooth Muscle	stomach
24	chrX:31213200-31215200	Weak transcription	Liver	Liver
25	chrX:31213800-31221000	Weak transcription	Gastric	stomach
26	chrX:31214000-31214800	Strong transcription	Hela-S3	cervix
27	chrX:31214200-31240600	Weak transcription	Brain Angular Gyrus	brain
28	chrX:31214600-31214800	Enhancers	Pancreas	Pancrea
29	chrX:31214800-31215200	Weak transcription	Pancreas	Pancrea
30	chrX:31214800-31216600	Genic enhancers	Hela-S3	cervix
31	chrX:31214800-31217400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chrX:31215200-31215400	Enhancers	Pancreas	Pancrea
33	chrX:31215200-31217200	Strong transcription	Liver	Liver
34	chrX:31215200-31250400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chrX:31215400-31219200	Weak transcription	Pancreas	Pancrea
36	chrX:31215600-31231400	Weak transcription	Fetal Muscle Leg	muscle
37	chrX:31215800-31222200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chrX:31215800-31222800	Weak transcription	Brain Anterior Caudate	brain
39	chrX:31216000-31217800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chrX:31216000-31227200	Weak transcription	HMEC	breast
41	chrX:31216000-31248200	Weak transcription	Psoas Muscle	Psoas
42	chrX:31216200-31216600	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chrX:31216400-31216600	Enhancers	Fetal Intestine Large	intestine
44	chrX:31216600-31217600	Weak transcription	Fetal Intestine Large	intestine
45	chrX:31216600-31218600	Enhancers	Hela-S3	cervix
46	chrX:31216600-31235400	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chrX:31216800-31218200	Enhancers	HUVEC	blood vessel
48	chrX:31217200-31217400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chrX:31217200-31218600	Enhancers	HepG2	liver
50	chrX:31217200-31219400	Weak transcription	Liver	Liver

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