Variant report

Variant	nsv481774
Chromosome Location	chrX:31749309-31964931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:61)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
4	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
5	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
6	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
7	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
8	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
9	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
10	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
11	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
12	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
13	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
14	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
15	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
16	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
17	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
18	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
19	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
20	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
21	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
22	CEBPB	chrX:31854765-31854950	K562	blood:	n/a	chrX:31854795-31854812
23	CEBPB	chrX:31880697-31881227	K562	blood:	n/a	n/a
24	CEBPB	chrX:31949303-31949614	HepG2	liver:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
25	CEBPB	chrX:31902669-31903009	K562	blood:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
26	CEBPB	chrX:31890217-31890462	K562	blood:	n/a	n/a
27	CEBPB	chrX:31912424-31912651	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chrX:31890153-31890439	K562	blood:	n/a	n/a
29	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
30	CEBPB	chrX:31902702-31902922	Hela-S3	cervix:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
31	CEBPB	chrX:31880877-31881207	K562	blood:	n/a	n/a
32	CEBPB	chrX:31763086-31763279	A549	lung:	n/a	n/a
33	CEBPB	chrX:31839449-31839744	K562	blood:	n/a	n/a
34	CEBPB	chrX:31778692-31778796	HepG2	liver:	n/a	n/a
35	CEBPB	chrX:31949323-31949654	IMR90	lung:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
36	CEBPB	chrX:31902680-31902999	HepG2	liver:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
37	CEBPB	chrX:31869466-31869539	K562	blood:	n/a	n/a
38	CEBPB	chrX:31839455-31839711	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chrX:31773913-31774042	HepG2	liver:	n/a	chrX:31773955-31773966 chrX:31773957-31773968
40	CEBPB	chrX:31826634-31826676	K562	blood:	n/a	n/a
41	CEBPB	chrX:31949328-31949638	K562	blood:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
42	CEBPB	chrX:31826556-31826776	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chrX:31949361-31949579	H1-hESC	embryonic stem cell:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
44	CEBPB	chrX:31902677-31902924	A549	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
45	CEBPD	chrX:31890132-31890577	K562	blood:	n/a	n/a
46	CEBPD	chrX:31888350-31888723	K562	blood:	n/a	n/a
47	CEBPD	chrX:31890131-31890556	K562	blood:	n/a	n/a
48	CEBPD	chrX:31865879-31866246	K562	blood:	n/a	n/a
49	CEBPD	chrX:31865787-31866260	K562	blood:	n/a	n/a
50	CHD2	chrX:31890070-31890404	K562	blood:	n/a	chrX:31890201-31890211

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31889692-31889742	CMK	blood:	n/a
2	chrX:31889692-31889742	RPTEC	kidney:	n/a
3	chrX:31889692-31889742	SK-N-SH_RA	brain:	n/a
4	chrX:31889692-31889742	PANC-1	pancreas:	n/a
5	chrX:31889692-31889742	HL-60	blood:	n/a
6	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
7	chrX:31889692-31889742	U87	brain:	n/a
8	chrX:31889692-31889742	PFSK-1	brain:	n/a
9	chrX:31889692-31889742	HMEC	breast:	n/a
10	chrX:31889692-31889742	Caco-2	colon:	n/a
11	chrX:31889692-31889742	AoSMC	blood vessel:	n/a
12	chrX:31889692-31889742	AG09309	skin:	n/a
13	chrX:31889692-31889742	HIPEpiC	eye:	n/a
14	chrX:31889692-31889742	HAEpiC	amniotic membrane:	n/a
15	chrX:31889692-31889742	NT2-D1	testis:	n/a
16	chrX:31889692-31889742	LNCaP	prostate:	n/a
17	chrX:31889692-31889742	GM12892	blood:	n/a
18	chrX:31889692-31889742	Hela-S3	cervix:	n/a
19	chrX:31889692-31889742	NHBE	bronchial:	n/a
20	chrX:31889692-31889742	ProgFib	skin:	n/a
21	chrX:31889692-31889742	K562	blood:	n/a
22	chrX:31889692-31889742	BE2_C	brain:	n/a
23	chrX:31889692-31889742	HRE	kidney:	n/a
24	chrX:31889692-31889742	A549	lung:	n/a
25	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
26	chrX:31889692-31889742	HPAEpiC	pulmonary alveolar:	n/a
27	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
28	chrX:31889692-31889742	BJ	skin:	n/a
29	chrX:31889692-31889742	GM06990	blood:	n/a
30	chrX:31889692-31889742	HRPEpiC	eye:	n/a
31	chrX:31889692-31889742	NHDF-neo	bronchial:	n/a
32	chrX:31889692-31889742	AG09319	gingival:	n/a
33	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
34	chrX:31889692-31889742	AG04449	skin:	fetal
35	chrX:31889692-31889742	SKMC	muscle:	n/a
36	chrX:31889692-31889742	SAEC	small airway:	n/a
37	chrX:31889692-31889742	PrEC	prostate:	n/a
38	chrX:31889692-31889742	Hepatocyte	liver:	n/a
39	chrX:31889692-31889742	HEEpiC	esophagus:	n/a
40	chrX:31889692-31889742	GM12878	blood:	n/a
41	chrX:31889692-31889742	HepG2	liver:	n/a
42	chrX:31889692-31889742	IMR90	lung:	fetal
43	chrX:31889692-31889742	GM19239	blood:	n/a
44	chrX:31889692-31889742	MCF-7	breast:	n/a
45	chrX:31889692-31889742	Jurkat	blood:	n/a
46	chrX:31889692-31889742	GM12891	blood:	n/a
47	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
48	chrX:31889692-31889742	T-47D	breast:	n/a
49	chrX:31889692-31889742	AG10803	skin:	n/a
50	chrX:31889692-31889742	ECC-1	luminal epithelium:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
2	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
3	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
4	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
5	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
6	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
7	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
8	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
9	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
10	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
11	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
12	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
13	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:
14	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
15	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
16	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
17	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
18	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
19	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
20	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
21	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
22	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
23	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
24	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
25	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
26	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
27	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
28	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
29	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
30	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
31	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
32	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
33	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
34	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
35	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
36	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
37	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
38	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
39	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
40	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
41	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
42	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:

No data

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

Extended variants
information (count: 2351 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2351 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138373356	chrX:31749367-31749368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143932153	chrX:31749423-31749424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10521977	chrX:31749463-31749464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs370928755	chrX:31749598-31749599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs16989800	chrX:31749599-31749600	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs186301294	chrX:31749912-31749913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189526370	chrX:31750022-31750023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149311449	chrX:31750053-31750054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375112104	chrX:31750178-31750179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199541506	chrX:31750289-31750290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144339552	chrX:31750290-31750291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10611415	chrX:31750291-31750292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180755911	chrX:31750338-31750339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186193944	chrX:31750450-31750451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191150255	chrX:31750525-31750526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12852598	chrX:31750557-31750558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183458545	chrX:31750579-31750580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144618804	chrX:31750646-31750647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186361036	chrX:31750666-31750667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368381047	chrX:31750693-31750694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148491655	chrX:31750771-31750772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529134124	chrX:31750814-31750815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190342165	chrX:31750997-31750998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182948256	chrX:31751002-31751003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187648416	chrX:31751182-31751183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192624797	chrX:31751261-31751262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182523275	chrX:31751376-31751377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188019915	chrX:31751587-31751588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113771047	chrX:31751752-31751753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376117245	chrX:31751805-31751806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184681933	chrX:31751809-31751810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188704646	chrX:31751973-31751974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12687049	chrX:31751996-31751997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112316301	chrX:31752008-31752009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192016477	chrX:31752058-31752059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373959279	chrX:31752098-31752099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184617921	chrX:31752147-31752148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139856305	chrX:31752195-31752196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189376773	chrX:31752265-31752266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201586876	chrX:31752332-31752333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547905261	chrX:31752341-31752342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2646301	chrX:31752343-31752344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185947452	chrX:31752345-31752346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189270998	chrX:31752360-31752361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180895785	chrX:31752388-31752389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs56042758	chrX:31752745-31752746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566228134	chrX:31752857-31752858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2738306	chrX:31752869-31752870	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs56326966	chrX:31753023-31753024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374616850	chrX:31753209-31753210	Weak transcription	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:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31734400-31754400	Weak transcription	Liver	Liver
2	chrX:31736600-31749800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chrX:31747800-31749400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chrX:31749800-31750200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chrX:31754200-31754600	Enhancers	Hela-S3	cervix
6	chrX:31754400-31754600	Enhancers	Liver	Liver
7	chrX:31763200-31763400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chrX:31765000-31765400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chrX:31765200-31765800	Enhancers	Brain Inferior Temporal Lobe	brain
10	chrX:31765400-31766400	Enhancers	Fetal Brain Male	brain
11	chrX:31765400-31767000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chrX:31765600-31766400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chrX:31765800-31766800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chrX:31766400-31770800	Weak transcription	Fetal Brain Male	brain
15	chrX:31766800-31770800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chrX:31769400-31770400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chrX:31770200-31770800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chrX:31770200-31771000	Enhancers	Fetal Brain Female	brain
19	chrX:31770200-31771200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chrX:31770400-31771800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chrX:31770600-31771000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chrX:31770600-31771000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chrX:31770600-31771200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chrX:31770600-31771400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chrX:31770600-31772000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chrX:31770800-31771000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
27	chrX:31770800-31771200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chrX:31770800-31771400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chrX:31770800-31771400	Enhancers	Fetal Brain Male	brain
30	chrX:31771400-31774200	Weak transcription	Fetal Brain Male	brain
31	chrX:31771800-31772200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chrX:31772200-31773000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chrX:31774200-31774400	Enhancers	Fetal Brain Male	brain
34	chrX:31774400-31774800	Bivalent Enhancer	Fetal Brain Male	brain
35	chrX:31774400-31774800	Enhancers	Fetal Heart	heart
36	chrX:31777800-31778400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chrX:31787400-31787800	Enhancers	HSMMtube	muscle
38	chrX:31789000-31797400	Weak transcription	Liver	Liver
39	chrX:31797400-31797600	Enhancers	Liver	Liver
40	chrX:31809400-31838800	Weak transcription	Aorta	Aorta
41	chrX:31810800-31811400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chrX:31815400-31817000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chrX:31816000-31816800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chrX:31816400-31816800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chrX:31816600-31816800	Enhancers	HSMMtube	muscle
46	chrX:31816800-31825200	Weak transcription	HSMMtube	muscle
47	chrX:31823400-31826200	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chrX:31824000-31827000	Enhancers	Liver	Liver
49	chrX:31825800-31827000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chrX:31825800-31827200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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