Variant report

Variant	nsv520230
Chromosome Location	chrX:31611075-31919659
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:911)
CpG islands
(count:61)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:911 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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:31890048-31890539	K562	blood:	n/a	n/a
3	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
5	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
6	ARID3A	chrX:31676512-31676712	HepG2	liver:	n/a	n/a
7	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
8	ATF1	chrX:31720398-31720650	K562	blood:	n/a	n/a
9	ATF1	chrX:31625409-31625543	K562	blood:	n/a	n/a
10	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
11	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
12	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
13	ATF2	chrX:31622908-31623328	GM12878	blood:	n/a	n/a
14	ATF2	chrX:31622845-31623312	GM12878	blood:	n/a	n/a
15	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
16	BACH1	chrX:31628530-31628567	K562	blood:	n/a	n/a
17	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
18	BATF	chrX:31622870-31623366	GM12878	blood:	n/a	chrX:31623346-31623355
19	BATF	chrX:31622862-31623383	GM12878	blood:	n/a	chrX:31623346-31623355
20	BCL11A	chrX:31622897-31623396	GM12878	blood:	n/a	n/a
21	BCL11A	chrX:31622993-31623321	GM12878	blood:	n/a	n/a
22	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
23	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
24	BCL3	chrX:31737849-31738258	GM12878	blood:	n/a	n/a
25	BCL3	chrX:31737905-31738230	GM12878	blood:	n/a	n/a
26	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
27	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
28	BHLHE40	chrX:31622917-31623247	GM12878	blood:	n/a	n/a
29	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
30	BRCA1	chrX:31716811-31716827	Hela-S3	cervix:	n/a	n/a
31	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
32	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
33	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
34	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
35	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
36	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
37	CEBPB	chrX:31745355-31745547	A549	lung:	n/a	n/a
38	CEBPB	chrX:31854765-31854950	K562	blood:	n/a	chrX:31854795-31854812
39	CEBPB	chrX:31778692-31778796	HepG2	liver:	n/a	n/a
40	CEBPB	chrX:31902677-31902924	A549	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
41	CEBPB	chrX:31739555-31739659	Hela-S3	cervix:	n/a	chrX:31739596-31739607
42	CEBPB	chrX:31826634-31826676	K562	blood:	n/a	n/a
43	CEBPB	chrX:31912424-31912651	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chrX:31688381-31688643	HepG2	liver:	n/a	chrX:31688510-31688521
45	CEBPB	chrX:31880697-31881227	K562	blood:	n/a	n/a
46	CEBPB	chrX:31720394-31720668	IMR90	lung:	n/a	n/a
47	CEBPB	chrX:31644631-31644823	HepG2	liver:	n/a	n/a
48	CEBPB	chrX:31839455-31839711	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chrX:31902680-31902999	HepG2	liver:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
50	CEBPB	chrX:31688352-31688552	IMR90	lung:	n/a	chrX:31688510-31688521

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31889692-31889742	U87	brain:	n/a
2	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
3	chrX:31889692-31889742	HRE	kidney:	n/a
4	chrX:31889692-31889742	NHBE	bronchial:	n/a
5	chrX:31889692-31889742	A549	lung:	n/a
6	chrX:31889692-31889742	RPTEC	kidney:	n/a
7	chrX:31889692-31889742	HCT-116	colon:	n/a
8	chrX:31889692-31889742	PFSK-1	brain:	n/a
9	chrX:31889692-31889742	GM12891	blood:	n/a
10	chrX:31889692-31889742	ovcar-3	ovarian:	n/a
11	chrX:31889692-31889742	SKMC	muscle:	n/a
12	chrX:31889692-31889742	PANC-1	pancreas:	n/a
13	chrX:31889692-31889742	ProgFib	skin:	n/a
14	chrX:31889692-31889742	AG09309	skin:	n/a
15	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
16	chrX:31889692-31889742	SK-N-SH_RA	brain:	n/a
17	chrX:31889692-31889742	AoSMC	blood vessel:	n/a
18	chrX:31889692-31889742	T-47D	breast:	n/a
19	chrX:31889692-31889742	MCF-7	breast:	n/a
20	chrX:31889692-31889742	GM06990	blood:	n/a
21	chrX:31889692-31889742	LNCaP	prostate:	n/a
22	chrX:31889692-31889742	AG09319	gingival:	n/a
23	chrX:31889692-31889742	HMEC	breast:	n/a
24	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
25	chrX:31889692-31889742	Hepatocyte	liver:	n/a
26	chrX:31889692-31889742	ECC-1	luminal epithelium:	n/a
27	chrX:31889692-31889742	HIPEpiC	eye:	n/a
28	chrX:31889692-31889742	CMK	blood:	n/a
29	chrX:31889692-31889742	NB4	blood:	n/a
30	chrX:31889692-31889742	K562	blood:	n/a
31	chrX:31889692-31889742	Hela-S3	cervix:	n/a
32	chrX:31889692-31889742	SK-N-SH	brain:	n/a
33	chrX:31889692-31889742	GM19239	blood:	n/a
34	chrX:31889692-31889742	HEK293	kidney:	embryo
35	chrX:31889692-31889742	SK-N-MC	brain:	n/a
36	chrX:31889692-31889742	NHDF-neo	bronchial:	n/a
37	chrX:31889692-31889742	SAEC	small airway:	n/a
38	chrX:31889692-31889742	HRPEpiC	eye:	n/a
39	chrX:31889692-31889742	AG04449	skin:	fetal
40	chrX:31889692-31889742	NH-A	brain:	n/a
41	chrX:31889692-31889742	GM12892	blood:	n/a
42	chrX:31889692-31889742	AG10803	skin:	n/a
43	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
44	chrX:31889692-31889742	HCM	heart:	n/a
45	chrX:31889692-31889742	BJ	skin:	n/a
46	chrX:31889692-31889742	Jurkat	blood:	n/a
47	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
48	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
49	chrX:31889692-31889742	HCF	heart:	n/a
50	chrX:31889692-31889742	PrEC	prostate:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
2	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
3	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
4	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
5	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
6	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
7	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
8	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
9	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
10	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
11	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
12	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
13	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
14	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
15	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
16	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
17	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
18	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
19	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
20	chrX:31056385..31057531-chrX:31676225..31677578,5	MCF-7	breast:
21	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
22	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
23	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
24	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
25	chr21:9824692..9827129-chrX:31658009..31660080,2	MCF-7	breast:
26	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
27	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
28	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
29	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
30	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
31	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
32	chr22:21979310..21981506-chrX:31657956..31659478,2	K562	blood:
33	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:
34	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
35	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
36	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
37	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
38	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
39	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
40	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
41	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
42	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
43	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
44	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
45	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
46	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
47	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
48	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
49	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
50	chrX:30954183..30954687-chrX:31676252..31677226,2	MCF-7	breast:

No data

Variant related genes	Relation type
DMD	TF binding region
DMD	CpG island
ENSG00000047597	chromatin interactions
ENSG00000106638	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000198947	chromatin interactions

Extended variants
information (count: 2846 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2846 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192950760	chrX:31619093-31619094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146380051	chrX:31619160-31619161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562744223	chrX:31619218-31619219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371565660	chrX:31619252-31619253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs200594852	chrX:31619332-31619333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139755724	chrX:31619350-31619351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34933251	chrX:31621805-31621806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375229391	chrX:31621860-31621861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189459193	chrX:31621875-31621876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527298167	chrX:31621880-31621881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181453376	chrX:31621966-31621967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148880129	chrX:31621984-31621985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143475782	chrX:31622006-31622007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148008353	chrX:31622012-31622013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186695358	chrX:31622034-31622035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563844180	chrX:31622390-31622391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7056449	chrX:31624585-31624586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546707769	chrX:31624602-31624603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189147663	chrX:31624638-31624639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7057494	chrX:31624708-31624709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs77901073	chrX:31624832-31624833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147239037	chrX:31624866-31624867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192592460	chrX:31624898-31624899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559830767	chrX:31624915-31624916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184172505	chrX:31624977-31624978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140733282	chrX:31625024-31625025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571411125	chrX:31625125-31625126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7883274	chrX:31625182-31625183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs80268218	chrX:31625213-31625214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140249357	chrX:31625222-31625223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149930142	chrX:31625308-31625309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145028420	chrX:31625370-31625371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140887100	chrX:31625640-31625641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144702675	chrX:31625651-31625652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs5927025	chrX:31625691-31625692	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs375646816	chrX:31625725-31625726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113640463	chrX:31625869-31625870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs55690014	chrX:31625884-31625885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73455913	chrX:31625932-31625933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200245155	chrX:31626022-31626023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371486122	chrX:31626025-31626026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79096760	chrX:31626054-31626055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376441456	chrX:31626061-31626062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189596188	chrX:31626136-31626137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs36075028	chrX:31626288-31626289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374604633	chrX:31626402-31626403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181205966	chrX:31626416-31626417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186759729	chrX:31626433-31626434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189047189	chrX:31626450-31626451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373789078	chrX:31626468-31626469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Pancreatic cancer	17952125	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	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
Colorectal cancer	21645411	CNVD
Ornithine transcarbamylase deficiency	21467225	CNVD
Myxofibrosarcoma	16751306	CNVD
Duchenne and Becker muscular dystrophies	18663755	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31619000-31619400	Enhancers	K562	blood
2	chrX:31621800-31622000	Enhancers	Muscle Satellite Cultured Cells	--
3	chrX:31621800-31622400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chrX:31624400-31625400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chrX:31625200-31625400	Enhancers	Hela-S3	cervix
6	chrX:31625200-31625800	Enhancers	HMEC	breast
7	chrX:31625200-31626000	Enhancers	NHEK	skin
8	chrX:31625400-31625600	Enhancers	Muscle Satellite Cultured Cells	--
9	chrX:31625400-31625800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chrX:31625400-31626800	Weak transcription	Hela-S3	cervix
11	chrX:31625600-31626800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chrX:31625600-31628000	Weak transcription	Liver	Liver
13	chrX:31625800-31626200	Weak transcription	HMEC	breast
14	chrX:31626000-31626400	Weak transcription	NHEK	skin
15	chrX:31626200-31628200	Enhancers	HMEC	breast
16	chrX:31626400-31628200	Enhancers	NHEK	skin
17	chrX:31626800-31627000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chrX:31626800-31627000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chrX:31626800-31627800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chrX:31626800-31628000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chrX:31626800-31628000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chrX:31626800-31628200	Enhancers	Muscle Satellite Cultured Cells	--
23	chrX:31626800-31628200	Enhancers	Hela-S3	cervix
24	chrX:31627000-31627600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chrX:31627000-31627800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chrX:31627600-31628200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chrX:31627800-31628000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chrX:31628000-31628200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
29	chrX:31628000-31633600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chrX:31629000-31629200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chrX:31630000-31632400	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chrX:31630200-31631600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chrX:31632400-31632800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chrX:31633600-31634200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chrX:31644600-31645400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chrX:31645200-31646200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chrX:31645200-31646200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chrX:31645400-31645800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chrX:31645400-31646000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chrX:31645400-31646000	Enhancers	Muscle Satellite Cultured Cells	--
41	chrX:31645600-31646000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chrX:31645600-31646000	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chrX:31645800-31646000	Enhancers	Colon Smooth Muscle	Colon
44	chrX:31645800-31646200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chrX:31645800-31646200	Active TSS	Brain Anterior Caudate	brain
46	chrX:31646000-31650000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chrX:31646200-31647400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chrX:31646200-31647600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chrX:31646200-31648200	Weak transcription	Brain Anterior Caudate	brain
50	chrX:31646400-31647800	Weak transcription	Colon Smooth Muscle	Colon

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