Variant report

Variant	nsv481764
Chromosome Location	chrX:31587315-31944285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1045)
CpG islands
(count:61)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1045 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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:31907685-31907977	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31676512-31676712	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
5	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
6	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
7	ATF1	chrX:31625409-31625543	K562	blood:	n/a	n/a
8	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
9	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
10	ATF1	chrX:31608896-31609186	K562	blood:	n/a	n/a
11	ATF1	chrX:31720398-31720650	K562	blood:	n/a	n/a
12	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
13	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
14	ATF2	chrX:31622845-31623312	GM12878	blood:	n/a	n/a
15	ATF2	chrX:31622908-31623328	GM12878	blood:	n/a	n/a
16	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
17	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
18	BACH1	chrX:31628530-31628567	K562	blood:	n/a	n/a
19	BATF	chrX:31622870-31623366	GM12878	blood:	n/a	chrX:31623346-31623355
20	BATF	chrX:31622862-31623383	GM12878	blood:	n/a	chrX:31623346-31623355
21	BCL11A	chrX:31622993-31623321	GM12878	blood:	n/a	n/a
22	BCL11A	chrX:31622897-31623396	GM12878	blood:	n/a	n/a
23	BCL3	chrX:31737849-31738258	GM12878	blood:	n/a	n/a
24	BCL3	chrX:31737905-31738230	GM12878	blood:	n/a	n/a
25	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
26	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
27	BHLHE40	chrX:31622917-31623247	GM12878	blood:	n/a	n/a
28	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
29	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
30	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
31	BRCA1	chrX:31716811-31716827	Hela-S3	cervix:	n/a	n/a
32	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
33	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
34	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
35	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
36	CCNT2	chrX:31608833-31609110	K562	blood:	n/a	n/a
37	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
38	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
39	CEBPB	chrX:31839455-31839711	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chrX:31739458-31739663	IMR90	lung:	n/a	chrX:31739596-31739607
41	CEBPB	chrX:31739446-31739711	H1-hESC	embryonic stem cell:	n/a	chrX:31739596-31739607
42	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
43	CEBPB	chrX:31609526-31609843	K562	blood:	n/a	chrX:31609679-31609690
44	CEBPB	chrX:31688352-31688552	IMR90	lung:	n/a	chrX:31688510-31688521
45	CEBPB	chrX:31763086-31763279	A549	lung:	n/a	n/a
46	CEBPB	chrX:31739551-31739655	A549	lung:	n/a	chrX:31739596-31739607
47	CEBPB	chrX:31627053-31627605	IMR90	lung:	n/a	chrX:31627336-31627353 chrX:31627337-31627350
48	CEBPB	chrX:31626911-31627652	Hela-S3	cervix:	n/a	chrX:31627336-31627353 chrX:31627337-31627350
49	CEBPB	chrX:31739488-31739744	HepG2	liver:	n/a	chrX:31739596-31739607
50	CEBPB	chrX:31676300-31676599	IMR90	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31889692-31889742	HMEC	breast:	n/a
2	chrX:31889692-31889742	HRE	kidney:	n/a
3	chrX:31889692-31889742	U87	brain:	n/a
4	chrX:31889692-31889742	BJ	skin:	n/a
5	chrX:31889692-31889742	GM12891	blood:	n/a
6	chrX:31889692-31889742	GM12892	blood:	n/a
7	chrX:31889692-31889742	NH-A	brain:	n/a
8	chrX:31889692-31889742	AG10803	skin:	n/a
9	chrX:31889692-31889742	NT2-D1	testis:	n/a
10	chrX:31889692-31889742	HPAEpiC	pulmonary alveolar:	n/a
11	chrX:31889692-31889742	RPTEC	kidney:	n/a
12	chrX:31889692-31889742	SAEC	small airway:	n/a
13	chrX:31889692-31889742	GM19239	blood:	n/a
14	chrX:31889692-31889742	HIPEpiC	eye:	n/a
15	chrX:31889692-31889742	SK-N-SH_RA	brain:	n/a
16	chrX:31889692-31889742	HCF	heart:	n/a
17	chrX:31889692-31889742	HEEpiC	esophagus:	n/a
18	chrX:31889692-31889742	HL-60	blood:	n/a
19	chrX:31889692-31889742	ECC-1	luminal epithelium:	n/a
20	chrX:31889692-31889742	NB4	blood:	n/a
21	chrX:31889692-31889742	GM06990	blood:	n/a
22	chrX:31889692-31889742	HCT-116	colon:	n/a
23	chrX:31889692-31889742	NHBE	bronchial:	n/a
24	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
25	chrX:31889692-31889742	HepG2	liver:	n/a
26	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
27	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
28	chrX:31889692-31889742	HEK293	kidney:	embryo
29	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
30	chrX:31889692-31889742	AG09319	gingival:	n/a
31	chrX:31889692-31889742	HRPEpiC	eye:	n/a
32	chrX:31889692-31889742	BE2_C	brain:	n/a
33	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
34	chrX:31889692-31889742	AG04449	skin:	fetal
35	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
36	chrX:31889692-31889742	HAEpiC	amniotic membrane:	n/a
37	chrX:31889692-31889742	SK-N-SH	brain:	n/a
38	chrX:31889692-31889742	A549	lung:	n/a
39	chrX:31889692-31889742	LNCaP	prostate:	n/a
40	chrX:31889692-31889742	T-47D	breast:	n/a
41	chrX:31889692-31889742	GM12878	blood:	n/a
42	chrX:31889692-31889742	MCF-7	breast:	n/a
43	chrX:31889692-31889742	AG09309	skin:	n/a
44	chrX:31889692-31889742	PANC-1	pancreas:	n/a
45	chrX:31889692-31889742	SKMC	muscle:	n/a
46	chrX:31889692-31889742	K562	blood:	n/a
47	chrX:31889692-31889742	CMK	blood:	n/a
48	chrX:31889692-31889742	Hela-S3	cervix:	n/a
49	chrX:31889692-31889742	SK-N-MC	brain:	n/a
50	chrX:31889692-31889742	ovcar-3	ovarian:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
2	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
3	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
4	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
5	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
6	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
7	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
8	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
9	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
10	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
11	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:
12	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
13	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
14	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
15	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
16	chr21:9824692..9827129-chrX:31658009..31660080,2	MCF-7	breast:
17	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
18	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
19	chrX:30954183..30954687-chrX:31676252..31677226,2	MCF-7	breast:
20	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
21	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
22	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
23	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
24	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
25	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
26	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
27	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
28	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
29	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
30	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
31	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
32	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
33	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
34	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
35	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
36	chrX:31056385..31057531-chrX:31676225..31677578,5	MCF-7	breast:
37	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
38	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
39	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
40	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
41	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
42	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
43	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
44	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
45	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
46	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
47	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
48	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
49	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
50	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:

No data

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

Extended variants
information (count: 3190 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3190 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190378974	chrX:31589824-31589825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182014311	chrX:31590030-31590031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113697408	chrX:31590031-31590032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554822857	chrX:31590080-31590081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187666057	chrX:31590086-31590087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143524948	chrX:31590204-31590205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190747727	chrX:31590240-31590241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146721894	chrX:31590275-31590276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542852541	chrX:31590353-31590354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs180711042	chrX:31590386-31590387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140357433	chrX:31590506-31590507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185102678	chrX:31590576-31590577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190003932	chrX:31590728-31590729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182589871	chrX:31590787-31590788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28538715	chrX:31590912-31590913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188281871	chrX:31590945-31590946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150962161	chrX:31590951-31590952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35257994	chrX:31591145-31591146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375875724	chrX:31591177-31591178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560927496	chrX:31591179-31591180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192068632	chrX:31591236-31591237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6527104	chrX:31591334-31591335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183816933	chrX:31591483-31591484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77914149	chrX:31598349-31598350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139406417	chrX:31598382-31598383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548717417	chrX:31598410-31598411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150557530	chrX:31598481-31598482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs180702433	chrX:31598591-31598592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79114651	chrX:31598785-31598786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185958091	chrX:31598853-31598854	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs189731766	chrX:31598862-31598863	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181331104	chrX:31598908-31598909	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs12687010	chrX:31598924-31598925	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs34068707	chrX:31599084-31599085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149685218	chrX:31599127-31599128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377192195	chrX:31599258-31599259	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs566961639	chrX:31599267-31599268	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs370377412	chrX:31599321-31599322	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs370697166	chrX:31599379-31599380	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs186028430	chrX:31599422-31599423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190744118	chrX:31599497-31599498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183361968	chrX:31599500-31599501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186567964	chrX:31599620-31599621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191072795	chrX:31599782-31599783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139409763	chrX:31599992-31599993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182619123	chrX:31600024-31600025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187678531	chrX:31600079-31600080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192850860	chrX:31600176-31600177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112953926	chrX:31600237-31600238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183147674	chrX:31600403-31600404	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:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31589800-31591600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chrX:31590400-31591200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chrX:31590400-31591400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chrX:31590600-31591200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chrX:31598200-31599400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chrX:31598200-31599400	Enhancers	NHDF-Ad	bronchial
7	chrX:31598200-31599600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chrX:31598200-31599600	Enhancers	HMEC	breast
9	chrX:31598200-31599600	Enhancers	NHEK	skin
10	chrX:31598200-31599800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chrX:31598400-31598800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chrX:31598400-31599000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chrX:31598400-31599400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chrX:31598400-31599600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chrX:31598400-31599600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chrX:31598400-31599600	Enhancers	HSMM	muscle
17	chrX:31598400-31599600	Enhancers	NH-A	brain
18	chrX:31598400-31600000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chrX:31598600-31598800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chrX:31598600-31599600	Enhancers	HUVEC	blood vessel
21	chrX:31598600-31599600	Enhancers	Osteobl	bone
22	chrX:31598600-31599800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chrX:31598800-31599000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chrX:31598800-31599200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chrX:31598800-31599400	Enhancers	Hela-S3	cervix
26	chrX:31598800-31599600	Enhancers	Muscle Satellite Cultured Cells	--
27	chrX:31599000-31599200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chrX:31599200-31599400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chrX:31599200-31599800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chrX:31599400-31599600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chrX:31599400-31601000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chrX:31599600-31601000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chrX:31599600-31601200	Weak transcription	HMEC	breast
34	chrX:31599600-31606200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chrX:31599600-31606400	Weak transcription	NHEK	skin
36	chrX:31599800-31603600	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chrX:31600000-31603800	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chrX:31600600-31601400	Enhancers	HSMMtube	muscle
39	chrX:31601000-31601600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chrX:31601200-31601400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chrX:31601200-31601600	Enhancers	HMEC	breast
42	chrX:31601600-31606000	Weak transcription	HMEC	breast
43	chrX:31603600-31604000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chrX:31603800-31604000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chrX:31604000-31607000	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chrX:31606000-31607800	Enhancers	HMEC	breast
47	chrX:31606200-31607200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chrX:31606400-31607200	Enhancers	NHEK	skin
49	chrX:31606400-31607400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chrX:31607000-31607400	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links