Variant report

Variant	nsv916218
Chromosome Location	chrX:79377399-80230929
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3744)
CpG islands
(count:2075)
Chromatin interactive
region (count:54)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3744 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:80065169-80065730	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:79546396-79546693	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:80066148-80066449	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:79767964-79768285	K562	blood:	n/a	n/a
5	ARID3A	chrX:79572188-79572290	K562	blood:	n/a	n/a
6	ARID3A	chrX:80104674-80104806	K562	blood:	n/a	n/a
7	ARID3A	chrX:80063628-80063882	HepG2	liver:	n/a	n/a
8	ARID3A	chrX:79573288-79573341	K562	blood:	n/a	n/a
9	ARID3A	chrX:79679347-79679597	K562	blood:	n/a	n/a
10	ATF1	chrX:80063304-80063846	K562	blood:	n/a	n/a
11	ATF1	chrX:79767797-79768237	K562	blood:	n/a	n/a
12	ATF1	chrX:80065275-80065874	K562	blood:	n/a	n/a
13	ATF3	chrX:79767807-79768213	K562	blood:	n/a	n/a
14	BACH1	chrX:79767877-79768214	K562	blood:	n/a	n/a
15	BACH1	chrX:80010901-80011084	K562	blood:	n/a	n/a
16	BACH1	chrX:79767895-79768209	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chrX:79490385-79490553	K562	blood:	n/a	n/a
18	BACH1	chrX:79679231-79679293	K562	blood:	n/a	n/a
19	BACH1	chrX:79919125-79919158	K562	blood:	n/a	n/a
20	BATF	chrX:79923475-79923845	GM12878	blood:	n/a	chrX:79923643-79923654
21	BATF	chrX:79767912-79768182	GM12878	blood:	n/a	n/a
22	BATF	chrX:79784820-79785018	GM12878	blood:	n/a	n/a
23	BCLAF1	chrX:80065310-80065811	GM12878	blood:	n/a	n/a
24	BCLAF1	chrX:80065338-80065818	GM12878	blood:	n/a	n/a
25	BHLHE40	chrX:80063596-80063898	GM12878	blood:	n/a	n/a
26	BHLHE40	chrX:79767829-79768229	K562	blood:	n/a	n/a
27	BHLHE40	chrX:80063629-80063789	K562	blood:	n/a	n/a
28	BHLHE40	chrX:80064147-80064417	GM12878	blood:	n/a	n/a
29	BHLHE40	chrX:80065452-80066181	HepG2	liver:	n/a	n/a
30	BHLHE40	chrX:79468414-79468681	K562	blood:	n/a	n/a
31	BHLHE40	chrX:80064992-80066246	GM12878	blood:	n/a	n/a
32	BHLHE40	chrX:79679331-79679531	K562	blood:	n/a	n/a
33	BHLHE40	chrX:80065195-80066400	K562	blood:	n/a	n/a
34	BHLHE40	chrX:80064549-80064712	K562	blood:	n/a	n/a
35	BHLHE40	chrX:79857544-79857912	K562	blood:	n/a	n/a
36	BRCA1	chrX:80065162-80066315	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chrX:80020735-80021377	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chrX:80063303-80064053	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chrX:80064037-80064046	GM12878	blood:	n/a	n/a
40	CBX3	chrX:79568006-79568290	K562	blood:	n/a	n/a
41	CBX3	chrX:79567956-79568323	K562	blood:	n/a	n/a
42	CBX3	chrX:79686916-79687325	K562	blood:	n/a	n/a
43	CBX3	chrX:79767923-79768263	K562	blood:	n/a	n/a
44	CBX3	chrX:79590622-79590841	K562	blood:	n/a	n/a
45	CBX3	chrX:79727512-79727752	K562	blood:	n/a	n/a
46	CBX3	chrX:79573202-79573538	K562	blood:	n/a	n/a
47	CBX3	chrX:79560825-79561078	K562	blood:	n/a	n/a
48	CBX3	chrX:79679158-79679638	K562	blood:	n/a	n/a
49	CBX3	chrX:79686968-79687268	K562	blood:	n/a	n/a
50	CBX3	chrX:80065337-80065825	K562	blood:	n/a	n/a

(count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:79830095-79830145	HAEpiC	amniotic membrane:	n/a
2	chrX:79830095-79830145	HAEpiC	amniotic membrane:	n/a
3	chrX:80065754-80065804	AG10803	skin:	n/a
4	chrX:79828776-79828826	A549	lung:	n/a
5	chrX:79830506-79830556	GM12891	blood:	n/a
6	chrX:80068613-80068663	MCF10A-Er-Src	breast:	n/a
7	chrX:79828920-79828970	LNCaP	prostate:	n/a
8	chrX:80065135-80065185	CMK	blood:	n/a
9	chrX:80061160-80061210	LNCaP	prostate:	n/a
10	chrX:79590874-79590924	SKMC	muscle:	n/a
11	chrX:79830095-79830145	HEK293	kidney:	embryo
12	chrX:79828776-79828826	HCF	heart:	n/a
13	chrX:79590966-79591016	ovcar-3	ovarian:	n/a
14	chrX:80065135-80065185	BJ	skin:	n/a
15	chrX:79590789-79590839	AG09309	skin:	n/a
16	chrX:79829286-79829336	NT2-D1	testis:	n/a
17	chrX:79830506-79830556	AG04449	skin:	fetal
18	chrX:79590905-79590955	K562	blood:	n/a
19	chrX:80064924-80064974	HAEpiC	amniotic membrane:	n/a
20	chrX:79830095-79830145	LNCaP	prostate:	n/a
21	chrX:79590825-79590875	HNPCEpiC	eye:	n/a
22	chrX:80065135-80065185	HCPEpiC	choroid plexus:	n/a
23	chrX:80064924-80064974	SK-N-SH	brain:	n/a
24	chrX:80068613-80068663	HCPEpiC	choroid plexus:	n/a
25	chrX:79829018-79829068	AG04449	skin:	fetal
26	chrX:79590825-79590875	ovcar-3	ovarian:	n/a
27	chrX:79590882-79590932	HEK293	kidney:	embryo
28	chrX:80068613-80068663	NHDF-neo	bronchial:	n/a
29	chrX:80065003-80065053	HCT-116	colon:	n/a
30	chrX:79830095-79830145	AG10803	skin:	n/a
31	chrX:80065003-80065053	CMK	blood:	n/a
32	chrX:79830173-79830223	NHDF-neo	bronchial:	n/a
33	chrX:79830173-79830223	Hela-S3	cervix:	n/a
34	chrX:79590882-79590932	AG09319	gingival:	n/a
35	chrX:80065003-80065053	HPAEpiC	pulmonary alveolar:	n/a
36	chrX:80063471-80063521	A549	lung:	n/a
37	chrX:79591129-79591179	HIPEpiC	eye:	n/a
38	chrX:80065793-80065843	GM06990	blood:	n/a
39	chrX:79590905-79590955	PANC-1	pancreas:	n/a
40	chrX:79830173-79830223	HRPEpiC	eye:	n/a
41	chrX:79590789-79590839	SAEC	small airway:	n/a
42	chrX:79830343-79830393	PANC-1	pancreas:	n/a
43	chrX:79590789-79590839	MCF10A-Er-Src	breast:	n/a
44	chrX:79828920-79828970	HCM	heart:	n/a
45	chrX:79590789-79590839	ECC-1	luminal epithelium:	n/a
46	chrX:79591129-79591179	K562	blood:	n/a
47	chrX:79590882-79590932	K562	blood:	n/a
48	chrX:79828776-79828826	ovcar-3	ovarian:	n/a
49	chrX:79590874-79590924	AoSMC	blood vessel:	n/a
50	chrX:79589737-79589787	HCT-116	colon:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:79798375..79801316-chrX:79803356..79806190,2	K562	blood:
2	chrX:80046721..80048869-chrX:80050793..80053452,2	K562	blood:
3	chrX:79806226..79806865-chrX:79903226..79903832,2	MCF-7	breast:
4	chrX:79537779..79538289-chrX:79903212..79904194,2	K562	blood:
5	chrX:80098720..80100983-chrX:80101839..80103863,2	K562	blood:
6	chrX:80055012..80057050-chrX:80061763..80065831,3	K562	blood:
7	chrX:79939388..79942339-chrX:80064753..80066960,2	K562	blood:
8	chrX:79486703..79489248-chrX:79490340..79493173,2	K562	blood:
9	chrX:79806226..79806865-chrX:79903226..79903832,2	MCF-7	breast:
10	chrX:79519176..79521297-chrX:79525383..79527941,2	MCF-7	breast:
11	chrX:79983222..79984949-chrX:79986691..79988254,2	MCF-7	breast:
12	chrX:79798375..79801316-chrX:79803356..79806190,2	K562	blood:
13	chrX:80069067..80071673-chrX:80073607..80076127,2	K562	blood:
14	chrX:79449588..79452264-chrX:79453154..79454725,2	MCF-7	breast:
15	chrX:80098720..80100983-chrX:80101839..80103863,2	K562	blood:
16	chrX:79519176..79521297-chrX:79525383..79527941,2	MCF-7	breast:
17	chrX:79589237..79591292-chrX:79783770..79785297,2	K562	blood:
18	chrX:79983222..79984949-chrX:79986691..79988254,2	MCF-7	breast:
19	chrX:80069067..80071673-chrX:80073607..80076127,2	K562	blood:
20	chrX:79668622..79671035-chrX:79673648..79675152,2	K562	blood:
21	chrX:79583477..79586435-chrX:79600479..79603448,2	K562	blood:
22	chr7:2979121..2979742-chrX:79546256..79547017,2	MCF-7	breast:
23	chrX:79828395..79829983-chrX:79832557..79834595,3	K562	blood:
24	chrX:79582672..79585796-chrX:79589911..79592917,3	K562	blood:
25	chrX:79833900..79834805-chrX:79903150..79903788,2	MCF-7	breast:
26	chr2:85765978..85766680-chrX:80065260..80066141,2	NB4	blood:
27	chrX:79987929..79989580-chrX:79990479..79992508,2	K562	blood:
28	chrX:80056733..80059659-chrX:80063754..80065563,2	K562	blood:
29	chrX:79771895..79774887-chrX:79774948..79776959,2	K562	blood:
30	chrX:79551425..79553078-chrX:79565650..79568542,2	K562	blood:
31	chrX:79583477..79586435-chrX:79600479..79603448,2	K562	blood:
32	chrX:79987929..79989580-chrX:79990479..79992508,2	K562	blood:
33	chrX:79486703..79489248-chrX:79490340..79493173,2	K562	blood:
34	chrX:79945916..79948256-chrX:79950332..79951865,2	K562	blood:
35	chrX:79805915..79806859-chrX:79833965..79834700,3	MCF-7	breast:
36	chrX:79668622..79671035-chrX:79673648..79675152,2	K562	blood:
37	chrX:79589237..79591292-chrX:79783770..79785297,2	K562	blood:
38	chrX:79691145..79692665-chrX:79696900..79698706,2	K562	blood:
39	chrX:80067488..80068198-chrX:80376211..80376936,2	MCF-7	breast:
40	chrX:79833900..79834805-chrX:79903150..79903788,2	MCF-7	breast:
41	chrX:80046721..80048869-chrX:80050793..80053452,2	K562	blood:
42	chrX:79537779..79538289-chrX:79903212..79904194,2	K562	blood:
43	chrX:79449588..79452264-chrX:79453154..79454725,2	MCF-7	breast:
44	chrX:79805915..79806859-chrX:79833965..79834700,3	MCF-7	breast:
45	chrX:80063567..80065637-chrX:80375984..80378858,4	K562	blood:
46	chrX:79828395..79829983-chrX:79832557..79834595,3	K562	blood:
47	chrX:79771895..79774887-chrX:79774948..79776959,2	K562	blood:
48	chrX:79535698..79538408-chrX:79546607..79549205,2	K562	blood:
49	chrX:79691145..79692665-chrX:79696900..79698706,2	K562	blood:
50	chrX:79687212..79689938-chrX:79702867..79705422,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM46D-2	chrX:79784536-79784836	NONHSAT137722
2	lnc-BRWD3-2	chrX:79528830-79528904	NONHSAT137720
3	lnc-FAM46D-2	chrX:79785245-79785526	NONHSAT137722
4	lnc-BRWD3-2	chrX:79565585-79565669	NONHSAT137720
5	lnc-FAM46D-1	chrX:80067610-80068219	XLOC_008020
6	lnc-BRWD3-2	chrX:79538080-79538104	NONHSAT137720
7	lnc-FAM46D-3	chrX:79924144-79924376	NONHSAT137723
8	lnc-FAM46D-4	chrX:79965427-79966204	NONHSAT137725
9	lnc-BRWD3-2	chrX:79546371-79546531	NONHSAT137720
10	lnc-BRWD3-2	chrX:79545351-79545399	NONHSAT137720
11	lnc-BRWD3-2	chrX:79545164-79545268	NONHSAT137720
12	lnc-FAM46D-1	chrX:80065677-80065744	XLOC_008020
13	lnc-HMGN5-3	chrX:79927172-79929717	NONHSAT137724

No data

Variant related genes	Relation type
CHMP1B2P	TF binding region
ENSG00000239008	TF binding region
HK2P1	TF binding region
VDAC1P1	TF binding region
ENSG00000228051	TF binding region
HNRNPH3P1	TF binding region
FAM46D	TF binding region
RNU6-493P	TF binding region
ENSG00000225715	TF binding region
BRWD3	TF binding region
RNU6-995P	TF binding region
CHMP1B2P	CpG island
ENSG00000239008	CpG island
HK2P1	CpG island
VDAC1P1	CpG island
ENSG00000228051	CpG island
HNRNPH3P1	CpG island
FAM46D	CpG island
RNU6-493P	CpG island
ENSG00000225715	CpG island
BRWD3	CpG island
RNU6-995P	CpG island
ENSG00000230247	chromatin interactions
ENSG00000165288	chromatin interactions
ENSG00000198157	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000215104	chromatin interactions
ENSG00000174016	chromatin interactions

Extended variants
information (count: 3596 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:3596 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373570933	chrX:79378221-79378222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142785499	chrX:79378223-79378224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs61631808	chrX:79378304-79378305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182756002	chrX:79378506-79378507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73498520	chrX:79378540-79378541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188124952	chrX:79378591-79378592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12861780	chrX:79392226-79392227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193183215	chrX:79392341-79392342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184217574	chrX:79392385-79392386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369069757	chrX:79392387-79392388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs367805183	chrX:79392541-79392542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35113522	chrX:79392652-79392653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539144481	chrX:79392694-79392695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73630363	chrX:79392766-79392767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373552539	chrX:79392829-79392830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555869069	chrX:79392830-79392831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34238982	chrX:79392906-79392907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189409529	chrX:79392955-79392956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12688422	chrX:79393166-79393167	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147273458	chrX:79393186-79393187	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148733064	chrX:79393283-79393284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142188890	chrX:79393385-79393386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs5912401	chrX:79393815-79393816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112917383	chrX:79393827-79393828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7056200	chrX:79393866-79393867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181726297	chrX:79393889-79393890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374742624	chrX:79393989-79393990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372271514	chrX:79394064-79394065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34324349	chrX:79394081-79394082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72205540	chrX:79394163-79394164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541376601	chrX:79394181-79394182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185111146	chrX:79394189-79394190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2179111	chrX:79394195-79394196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189608237	chrX:79394234-79394235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541795	chrX:79394309-79394310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs180839230	chrX:79394321-79394322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186661826	chrX:79394324-79394325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4615729	chrX:79394440-79394441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191106103	chrX:79394616-79394617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1927057	chrX:79394646-79394647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183744893	chrX:79394702-79394703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1927056	chrX:79394726-79394727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185994023	chrX:79394745-79394746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191054183	chrX:79394851-79394852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183254282	chrX:79394862-79394863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187860844	chrX:79395002-79395003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192811279	chrX:79395008-79395009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182486957	chrX:79395097-79395098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188402855	chrX:79395131-79395132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192606993	chrX:79395217-79395218	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	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
Autism	22495311	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Premature ovarian failure	20952765	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1978 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:79378000-79378600	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chrX:79392200-79392800	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chrX:79392400-79393000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chrX:79392600-79393200	Enhancers	H1 Cell Line	embryonic stem cell
5	chrX:79393000-79393200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chrX:79393200-79393400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chrX:79393400-79395000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chrX:79395000-79395600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chrX:79395000-79395800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chrX:79427800-79430600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chrX:79429600-79430800	Enhancers	Stomach Mucosa	stomach
12	chrX:79429600-79431800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chrX:79429800-79430600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chrX:79430600-79431000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chrX:79430600-79431000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chrX:79430800-79432000	Weak transcription	Stomach Mucosa	stomach
17	chrX:79431000-79431400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chrX:79431000-79431600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chrX:79435400-79436400	Weak transcription	Stomach Mucosa	stomach
20	chrX:79436400-79438400	Enhancers	Stomach Mucosa	stomach
21	chrX:79436800-79437000	Bivalent Enhancer	Ovary	ovary
22	chrX:79456400-79456800	Active TSS	K562	blood
23	chrX:79456800-79457600	Weak transcription	K562	blood
24	chrX:79457600-79458000	Active TSS	K562	blood
25	chrX:79458000-79462400	Weak transcription	K562	blood
26	chrX:79460600-79460800	Enhancers	Stomach Mucosa	stomach
27	chrX:79460800-79461800	Weak transcription	Stomach Mucosa	stomach
28	chrX:79461800-79462400	Enhancers	Stomach Mucosa	stomach
29	chrX:79462400-79462800	Enhancers	K562	blood
30	chrX:79468800-79469400	Enhancers	HMEC	breast
31	chrX:79469400-79469600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chrX:79471400-79472000	Enhancers	A549	lung
33	chrX:79471800-79472400	Enhancers	Hela-S3	cervix
34	chrX:79472000-79472200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chrX:79472000-79473400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chrX:79478600-79479600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chrX:79478600-79481000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chrX:79478800-79479000	Active TSS	Monocytes-CD14+_RO01746	blood
39	chrX:79479000-79479400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chrX:79479400-79480000	Active TSS	Monocytes-CD14+_RO01746	blood
41	chrX:79479600-79480000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chrX:79480000-79480200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
43	chrX:79480000-79480200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chrX:79480200-79480800	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chrX:79480800-79481000	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chrX:79485000-79485800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chrX:79486000-79487600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chrX:79487200-79489600	Weak transcription	Fetal Intestine Small	intestine
49	chrX:79487600-79489200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chrX:79489200-79499400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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