Variant report

Variant	nsv481964
Chromosome Location	chrX:31270220-31672751
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2275)
CpG islands
(count:1100)
Chromatin interactive
region (count:22)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2275 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31655046-31655134	K562	blood:	n/a	n/a
2	ARID3A	chrX:31442158-31442355	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31558422-31558741	K562	blood:	n/a	n/a
4	ARID3A	chrX:31368398-31368911	HepG2	liver:	n/a	n/a
5	ARID3A	chrX:31292505-31292520	K562	blood:	n/a	n/a
6	ARID3A	chrX:31284124-31284273	HepG2	liver:	n/a	n/a
7	ARID3A	chrX:31374459-31375489	HepG2	liver:	n/a	chrX:31374966-31374982
8	ARID3A	chrX:31441684-31441786	K562	blood:	n/a	n/a
9	ARID3A	chrX:31283251-31283891	HepG2	liver:	n/a	n/a
10	ARID3A	chrX:31562099-31562120	K562	blood:	n/a	n/a
11	ATF1	chrX:31625409-31625543	K562	blood:	n/a	n/a
12	ATF1	chrX:31299839-31299907	K562	blood:	n/a	n/a
13	ATF1	chrX:31390110-31390428	K562	blood:	n/a	n/a
14	ATF1	chrX:31608896-31609186	K562	blood:	n/a	n/a
15	ATF1	chrX:31561944-31562144	K562	blood:	n/a	n/a
16	ATF1	chrX:31341826-31342081	K562	blood:	n/a	n/a
17	ATF1	chrX:31312610-31312891	K562	blood:	n/a	n/a
18	ATF1	chrX:31581912-31582258	K562	blood:	n/a	n/a
19	ATF1	chrX:31573635-31574055	K562	blood:	n/a	n/a
20	ATF2	chrX:31622845-31623312	GM12878	blood:	n/a	n/a
21	ATF2	chrX:31622908-31623328	GM12878	blood:	n/a	n/a
22	ATF3	chrX:31581903-31582162	K562	blood:	n/a	n/a
23	BACH1	chrX:31461975-31462162	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chrX:31284456-31284765	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chrX:31517260-31517602	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chrX:31628530-31628567	K562	blood:	n/a	n/a
27	BATF	chrX:31622870-31623366	GM12878	blood:	n/a	chrX:31623346-31623355
28	BATF	chrX:31290611-31290947	GM12878	blood:	n/a	n/a
29	BATF	chrX:31622862-31623383	GM12878	blood:	n/a	chrX:31623346-31623355
30	BCL11A	chrX:31622993-31623321	GM12878	blood:	n/a	n/a
31	BCL11A	chrX:31622897-31623396	GM12878	blood:	n/a	n/a
32	BHLHE40	chrX:31582083-31582277	K562	blood:	n/a	n/a
33	BHLHE40	chrX:31622917-31623247	GM12878	blood:	n/a	n/a
34	BHLHE40	chrX:31341800-31341935	GM12878	blood:	n/a	n/a
35	BHLHE40	chrX:31290652-31290893	GM12878	blood:	n/a	n/a
36	BHLHE40	chrX:31361626-31361856	HepG2	liver:	n/a	n/a
37	BHLHE40	chrX:31361587-31361844	K562	blood:	n/a	n/a
38	BRCA1	chrX:31564152-31564544	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chrX:31312893-31312899	GM12878	blood:	n/a	n/a
40	BRCA1	chrX:31441491-31442399	Hela-S3	cervix:	n/a	chrX:31442354-31442361
41	BRCA1	chrX:31439052-31439392	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chrX:31370954-31371737	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chrX:31350996-31351160	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chrX:31284844-31284909	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chrX:31374799-31375406	Hela-S3	cervix:	n/a	n/a
46	CCNT2	chrX:31608833-31609110	K562	blood:	n/a	n/a
47	CCNT2	chrX:31341783-31342043	K562	blood:	n/a	n/a
48	CCNT2	chrX:31350144-31350353	K562	blood:	n/a	n/a
49	CCNT2	chrX:31390189-31390389	K562	blood:	n/a	chrX:31390263-31390283
50	CCNT2	chrX:31312607-31312933	K562	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31285009-31285059	Jurkat	blood:	n/a
2	chrX:31285029-31285079	BE2_C	brain:	n/a
3	chrX:31285009-31285059	Jurkat	blood:	n/a
4	chrX:31285029-31285079	BE2_C	brain:	n/a
5	chrX:31284505-31284555	SK-N-MC	brain:	n/a
6	chrX:31285204-31285254	NT2-D1	testis:	n/a
7	chrX:31285489-31285539	ProgFib	skin:	n/a
8	chrX:31526745-31526795	HIPEpiC	eye:	n/a
9	chrX:31285032-31285082	HNPCEpiC	eye:	n/a
10	chrX:31284448-31284498	PFSK-1	brain:	n/a
11	chrX:31284813-31284863	PANC-1	pancreas:	n/a
12	chrX:31526531-31526581	LNCaP	prostate:	n/a
13	chrX:31285501-31285551	PFSK-1	brain:	n/a
14	chrX:31287275-31287325	IMR90	lung:	fetal
15	chrX:31285029-31285079	HEEpiC	esophagus:	n/a
16	chrX:31283706-31283756	GM06990	blood:	n/a
17	chrX:31284505-31284555	HCF	heart:	n/a
18	chrX:31285489-31285539	AG10803	skin:	n/a
19	chrX:31285018-31285068	HMEC	breast:	n/a
20	chrX:31283706-31283756	SK-N-SH_RA	brain:	n/a
21	chrX:31526531-31526581	PrEC	prostate:	n/a
22	chrX:31285029-31285079	HNPCEpiC	eye:	n/a
23	chrX:31285501-31285551	HNPCEpiC	eye:	n/a
24	chrX:31285032-31285082	SK-N-SH_RA	brain:	n/a
25	chrX:31285105-31285155	HRE	kidney:	n/a
26	chrX:31284813-31284863	GM19239	blood:	n/a
27	chrX:31285492-31285542	H1-hESC	embryonic stem cell:	embryo
28	chrX:31285204-31285254	AG09319	gingival:	n/a
29	chrX:31287275-31287325	HPAEpiC	pulmonary alveolar:	n/a
30	chrX:31285204-31285254	HNPCEpiC	eye:	n/a
31	chrX:31284505-31284555	MCF10A-Er-Src	breast:	n/a
32	chrX:31526745-31526795	NB4	blood:	n/a
33	chrX:31285501-31285551	T-47D	breast:	n/a
34	chrX:31526531-31526581	HCF	heart:	n/a
35	chrX:31285492-31285542	AG09309	skin:	n/a
36	chrX:31526531-31526581	HepG2	liver:	n/a
37	chrX:31284448-31284498	Caco-2	colon:	n/a
38	chrX:31285492-31285542	SKMC	muscle:	n/a
39	chrX:31526531-31526581	HUVEC	blood vessel:	n/a
40	chrX:31285018-31285068	RPTEC	kidney:	n/a
41	chrX:31282451-31282501	T-47D	breast:	n/a
42	chrX:31285489-31285539	NHBE	bronchial:	n/a
43	chrX:31282451-31282501	AG04449	skin:	fetal
44	chrX:31285489-31285539	HRCEpiC	kidney:	n/a
45	chrX:31285489-31285539	LNCaP	prostate:	n/a
46	chrX:31283706-31283756	Jurkat	blood:	n/a
47	chrX:31285105-31285155	GM12878	blood:	n/a
48	chrX:31282451-31282501	H1-hESC	embryonic stem cell:	embryo
49	chrX:31284505-31284555	ProgFib	skin:	n/a
50	chrX:31285029-31285079	AoSMC	blood vessel:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31256880..31259581-chrX:31282243..31284046,2	K562	blood:
2	chrX:31316037..31318700-chrX:31321039..31322657,2	K562	blood:
3	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:
4	chrX:31055216..31055947-chrX:31311393..31312206,2	MCF-7	breast:
5	chrX:31436407..31439307-chrX:31440950..31442473,2	K562	blood:
6	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
7	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
8	chrX:31231843..31232710-chrX:31311329..31312068,2	MCF-7	breast:
9	chrX:31311122..31313355-chrX:31314263..31316652,2	K562	blood:
10	chr22:21979310..21981506-chrX:31657956..31659478,2	K562	blood:
11	chrX:31311122..31313355-chrX:31314263..31316652,2	K562	blood:
12	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
13	chr5:43121100..43121993-chrX:31284323..31285114,2	Hela-S3	cervix:
14	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
15	chrX:31316037..31318700-chrX:31321039..31322657,2	K562	blood:
16	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:
17	chr21:9824692..9827129-chrX:31658009..31660080,2	MCF-7	breast:
18	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
19	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
20	chrX:31436407..31439307-chrX:31440950..31442473,2	K562	blood:
21	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
22	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTHL17-1	chrX:31279073-31279133	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

No data

Variant related genes	Relation type
DMD	TF binding region
RNU6-894P	TF binding region
DMD	CpG island
RNU6-894P	CpG island
ENSG00000264063	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000264462	chromatin interactions

Extended variants
information (count: 4645 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4645 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190085293	chrX:31270228-31270229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140286500	chrX:31270253-31270254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529613937	chrX:31270318-31270319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548354321	chrX:31270363-31270364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181278450	chrX:31270423-31270424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373705934	chrX:31270429-31270430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1573952	chrX:31270444-31270445	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs1573953	chrX:31270474-31270475	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185811226	chrX:31270505-31270506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs16998162	chrX:31270689-31270690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201499722	chrX:31270745-31270746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113601031	chrX:31270796-31270797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35747302	chrX:31270816-31270817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200120493	chrX:31270819-31270820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183534936	chrX:31270853-31270854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113369079	chrX:31270955-31270956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs55895542	chrX:31271006-31271007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6527076	chrX:31271031-31271032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188880607	chrX:31271033-31271034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112798359	chrX:31271050-31271051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11368058	chrX:31271107-31271108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200413271	chrX:31271541-31271542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7473029	chrX:31271558-31271559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191994629	chrX:31271627-31271628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78825788	chrX:31271709-31271710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1316798	chrX:31271731-31271732	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs182808708	chrX:31271909-31271910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186974862	chrX:31272093-31272094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17340630	chrX:31272225-31272226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144713324	chrX:31272235-31272236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148461124	chrX:31272246-31272247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377295006	chrX:31272388-31272389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201996687	chrX:31272455-31272456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542955599	chrX:31272559-31272560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6631284	chrX:31272566-31272567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150597346	chrX:31272649-31272650	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191707783	chrX:31272829-31272830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184023811	chrX:31272841-31272842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112428088	chrX:31272974-31272975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs66591448	chrX:31273001-31273002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs58840411	chrX:31273010-31273011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146666017	chrX:31273076-31273077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200072850	chrX:31273160-31273161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187245853	chrX:31273215-31273216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73617062	chrX:31273219-31273220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7890835	chrX:31273238-31273239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185196755	chrX:31273301-31273302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545864908	chrX:31273321-31273322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190599351	chrX:31273323-31273324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182324465	chrX:31273412-31273413	Weak transcription Strong transcription	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:1305 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31235000-31282000	Weak transcription	Left Ventricle	heart
2	chrX:31243200-31281800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chrX:31245200-31282000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chrX:31245400-31284000	Weak transcription	HSMMtube	muscle
5	chrX:31245600-31279800	Weak transcription	HepG2	liver
6	chrX:31247000-31280200	Weak transcription	Pancreas	Pancrea
7	chrX:31254000-31283200	Weak transcription	Fetal Intestine Small	intestine
8	chrX:31254200-31275200	Weak transcription	Liver	Liver
9	chrX:31257000-31282800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chrX:31264000-31282200	Weak transcription	Fetal Muscle Leg	muscle
11	chrX:31264600-31279800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chrX:31264800-31282400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chrX:31268800-31278400	Weak transcription	HMEC	breast
14	chrX:31270000-31273200	Weak transcription	Hela-S3	cervix
15	chrX:31270000-31280800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chrX:31271600-31271800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chrX:31271800-31272200	Enhancers	Brain Angular Gyrus	brain
18	chrX:31271800-31279600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chrX:31271800-31280000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chrX:31272200-31272600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chrX:31272200-31280800	Weak transcription	Brain Angular Gyrus	brain
22	chrX:31272600-31272800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chrX:31272800-31284400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chrX:31273200-31275600	Strong transcription	Hela-S3	cervix
25	chrX:31273600-31280200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chrX:31273600-31281000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chrX:31273800-31279800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chrX:31274400-31282400	Weak transcription	Ovary	ovary
29	chrX:31274400-31283600	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chrX:31275200-31276400	Strong transcription	Liver	Liver
31	chrX:31275600-31276200	Weak transcription	Hela-S3	cervix
32	chrX:31275800-31280800	Weak transcription	GM12878-XiMat	blood
33	chrX:31276200-31276600	Enhancers	Hela-S3	cervix
34	chrX:31276200-31276600	Enhancers	HUVEC	blood vessel
35	chrX:31276200-31276600	Enhancers	NHEK	skin
36	chrX:31276200-31276800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chrX:31276400-31276600	Enhancers	Brain Inferior Temporal Lobe	brain
38	chrX:31276400-31280800	Weak transcription	Liver	Liver
39	chrX:31276600-31277400	Weak transcription	Hela-S3	cervix
40	chrX:31276600-31280800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chrX:31276600-31283600	Weak transcription	HUVEC	blood vessel
42	chrX:31276800-31281800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chrX:31277400-31277600	Genic enhancers	Hela-S3	cervix
44	chrX:31277600-31278600	Strong transcription	Hela-S3	cervix
45	chrX:31278200-31282400	Weak transcription	Brain Germinal Matrix	brain
46	chrX:31278400-31279200	Enhancers	HMEC	breast
47	chrX:31278600-31280000	Genic enhancers	Hela-S3	cervix
48	chrX:31279200-31280800	Weak transcription	HMEC	breast
49	chrX:31279600-31283000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chrX:31279800-31280200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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