Variant report

Variant	nsv520699
Chromosome Location	chrX:154774663-154929412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:818)
CpG islands
(count:796)
Chromatin interactive
region (count:21)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:154841982-154842276	HepG2	liver:	n/a	n/a
2	ATF1	chrX:154839621-154839764	K562	blood:	n/a	n/a
3	BACH1	chrX:154842120-154842509	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chrX:154843368-154843558	K562	blood:	n/a	n/a
5	BHLHE40	chrX:154842475-154842802	GM12878	blood:	n/a	n/a
6	BHLHE40	chrX:154842005-154842825	K562	blood:	n/a	n/a
7	BRCA1	chrX:154842147-154842758	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chrX:154917275-154917410	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chrX:154907451-154907479	GM12878	blood:	n/a	n/a
10	CBX3	chrX:154842466-154842807	K562	blood:	n/a	n/a
11	CCNT2	chrX:154842068-154842819	K562	blood:	n/a	chrX:154842577-154842586
12	CEBPB	chrX:154846907-154847242	K562	blood:	n/a	n/a
13	CEBPB	chrX:154851388-154851607	IMR90	lung:	n/a	chrX:154851511-154851522
14	CEBPB	chrX:154812365-154812569	HepG2	liver:	n/a	chrX:154812540-154812551
15	CEBPB	chrX:154812526-154812724	A549	lung:	n/a	chrX:154812540-154812551
16	CEBPB	chrX:154854469-154854759	IMR90	lung:	n/a	chrX:154854622-154854633
17	CEBPB	chrX:154854525-154854748	HepG2	liver:	n/a	chrX:154854622-154854633
18	CEBPB	chrX:154787278-154787539	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chrX:154882407-154882618	HepG2	liver:	n/a	chrX:154882478-154882489
20	CEBPB	chrX:154882319-154882589	IMR90	lung:	n/a	chrX:154882478-154882489
21	CEBPB	chrX:154812536-154812558	Hela-S3	cervix:	n/a	chrX:154812540-154812551
22	CEBPB	chrX:154846937-154847221	A549	lung:	n/a	n/a
23	CEBPB	chrX:154787272-154787576	A549	lung:	n/a	n/a
24	CEBPB	chrX:154787278-154787542	K562	blood:	n/a	n/a
25	CEBPB	chrX:154814020-154814246	A549	lung:	n/a	n/a
26	CEBPB	chrX:154841932-154842743	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chrX:154851348-154851692	HepG2	liver:	n/a	chrX:154851511-154851522
28	CEBPB	chrX:154846928-154847229	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:154882342-154882630	A549	lung:	n/a	chrX:154882478-154882489
30	CEBPB	chrX:154812373-154812720	IMR90	lung:	n/a	chrX:154812540-154812551
31	CEBPB	chrX:154882311-154882639	K562	blood:	n/a	chrX:154882478-154882489
32	CEBPB	chrX:154787301-154787579	HepG2	liver:	n/a	n/a
33	CEBPB	chrX:154787303-154787608	IMR90	lung:	n/a	n/a
34	CEBPD	chrX:154896403-154896871	K562	blood:	n/a	n/a
35	CEBPD	chrX:154896428-154896716	K562	blood:	n/a	n/a
36	CHD1	chrX:154841880-154842389	GM12878	blood:	n/a	n/a
37	CHD2	chrX:154842388-154842767	HepG2	liver:	n/a	n/a
38	CHD2	chrX:154841902-154842825	Hela-S3	cervix:	n/a	n/a
39	CHD2	chrX:154842164-154842756	GM12878	blood:	n/a	n/a
40	CHD2	chrX:154842021-154842812	K562	blood:	n/a	n/a
41	CREB1	chrX:154841956-154842791	HepG2	liver:	n/a	n/a
42	CREB1	chrX:154842395-154842747	A549	lung:	n/a	n/a
43	CREB1	chrX:154842067-154842364	A549	lung:	n/a	n/a
44	CREB1	chrX:154842069-154842372	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chrX:154874860-154875010	GM12875	blood:	n/a	n/a
46	CTCF	chrX:154892100-154892250	HEK293	kidney:	n/a	n/a
47	CTCF	chrX:154880960-154881110	GM12874	blood:	n/a	n/a
48	CTCF	chrX:154892120-154892270	GM12867	blood:	n/a	n/a
49	CTCF	chrX:154916062-154916268	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chrX:154892158-154892202	GM13977	blood:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:154842856-154842906	SK-N-SH_RA	brain:	n/a
2	chrX:154839539-154839589	IMR90	lung:	fetal
3	chrX:154842689-154842739	AG10803	skin:	n/a
4	chrX:154842856-154842906	SK-N-SH_RA	brain:	n/a
5	chrX:154839539-154839589	IMR90	lung:	fetal
6	chrX:154842689-154842739	AG10803	skin:	n/a
7	chrX:154842689-154842739	NT2-D1	testis:	n/a
8	chrX:154842736-154842786	BJ	skin:	n/a
9	chrX:154842856-154842906	GM19239	blood:	n/a
10	chrX:154843228-154843278	GM19239	blood:	n/a
11	chrX:154843228-154843278	NHDF-neo	bronchial:	n/a
12	chrX:154842296-154842346	NB4	blood:	n/a
13	chrX:154842736-154842786	SKMC	muscle:	n/a
14	chrX:154842064-154842114	NT2-D1	testis:	n/a
15	chrX:154842064-154842114	NB4	blood:	n/a
16	chrX:154845915-154845965	HCM	heart:	n/a
17	chrX:154842296-154842346	H1-hESC	embryonic stem cell:	embryo
18	chrX:154842841-154842891	GM06990	blood:	n/a
19	chrX:154842856-154842906	SAEC	small airway:	n/a
20	chrX:154842689-154842739	HCPEpiC	choroid plexus:	n/a
21	chrX:154842064-154842114	MCF10A-Er-Src	breast:	n/a
22	chrX:154845915-154845965	ProgFib	skin:	n/a
23	chrX:154842320-154842370	BJ	skin:	n/a
24	chrX:154843228-154843278	HEEpiC	esophagus:	n/a
25	chrX:154842718-154842768	HCPEpiC	choroid plexus:	n/a
26	chrX:154842718-154842768	AG09309	skin:	n/a
27	chrX:154842535-154842585	GM12891	blood:	n/a
28	chrX:154842736-154842786	HRCEpiC	kidney:	n/a
29	chrX:154845915-154845965	NB4	blood:	n/a
30	chrX:154842718-154842768	NHBE	bronchial:	n/a
31	chrX:154842516-154842566	HCM	heart:	n/a
32	chrX:154842296-154842346	HEEpiC	esophagus:	n/a
33	chrX:154842841-154842891	ProgFib	skin:	n/a
34	chrX:154842320-154842370	GM06990	blood:	n/a
35	chrX:154839539-154839589	NT2-D1	testis:	n/a
36	chrX:154842856-154842906	HL-60	blood:	n/a
37	chrX:154842856-154842906	NHDF-neo	bronchial:	n/a
38	chrX:154842856-154842906	K562	blood:	n/a
39	chrX:154842296-154842346	AG09319	gingival:	n/a
40	chrX:154843228-154843278	GM12892	blood:	n/a
41	chrX:154842736-154842786	PANC-1	pancreas:	n/a
42	chrX:154842841-154842891	GM12892	blood:	n/a
43	chrX:154842535-154842585	Hela-S3	cervix:	n/a
44	chrX:154842841-154842891	HEK293	kidney:	embryo
45	chrX:154842736-154842786	HIPEpiC	eye:	n/a
46	chrX:154842535-154842585	HUVEC	blood vessel:	n/a
47	chrX:154839539-154839589	LNCaP	prostate:	n/a
48	chrX:154842718-154842768	HCM	heart:	n/a
49	chrX:154842718-154842768	HRCEpiC	kidney:	n/a
50	chrX:154842064-154842114	PFSK-1	brain:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:56965360..56966110-chrX:154842055..154842646,2	Hela-S3	cervix:
2	chrX:154821010..154823368-chrX:154829376..154831463,2	MCF-7	breast:
3	chrX:154835185..154837494-chrX:154841586..154844153,3	MCF-7	breast:
4	chrX:154830345..154832030-chrX:154841051..154843638,2	MCF-7	breast:
5	chrX:154852759..154855145-chrX:154855456..154857443,2	MCF-7	breast:
6	chrX:154820529..154823135-chrX:154841113..154843873,2	K562	blood:
7	chrX:154839050..154840725-chrX:154844182..154846436,2	K562	blood:
8	chrX:154821966..154823918-chrX:154841465..154843620,2	MCF-7	breast:
9	chrX:154828823..154830576-chrX:154834582..154837184,2	K562	blood:
10	chrX:154852759..154855145-chrX:154855456..154857443,2	MCF-7	breast:
11	chrX:154841306..154843483-chrX:154852668..154855499,2	K562	blood:
12	chrX:154899237..154900918-chrX:154908592..154911481,2	K562	blood:
13	chrX:154764181..154765520-chrX:154880551..154881570,5	MCF-7	breast:
14	chrX:154828823..154830576-chrX:154834582..154837184,2	K562	blood:
15	chrX:154841131..154843128-chrX:154843754..154848336,4	MCF-7	breast:
16	chrX:154821010..154823368-chrX:154829376..154831463,2	MCF-7	breast:
17	chrX:154839050..154840725-chrX:154844182..154846436,2	K562	blood:
18	chrX:154841993..154844299-chrX:154869880..154871886,2	MCF-7	breast:
19	chr12:49627964..49628871-chrX:154842972..154843491,2	Hela-S3	cervix:
20	chrX:154842449..154844319-chrX:154844687..154848376,3	K562	blood:
21	chr17:41150074..41150665-chrX:154841732..154842592,2	Hela-S3	cervix:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-H2AFB3-2	chrX:154841789-154842265	NONHSAT139244
2	lnc-F8A2-2	chrX:154841135-154841277	ENSG00000224533.3
3	lnc-H2AFB3-2	chrX:154842453-154842556	NONHSAT139244
4	lnc-TMLHE-2	chrX:154774828-154774938	NONHSAT139243
5	lnc-TMLHE-2	chrX:154899419-154899605	NONHSAT139243

No data

Variant related genes	Relation type
TMLHE	TF binding region
TMLHE	CpG island
ENSG00000051108	chromatin interactions
ENSG00000185973	chromatin interactions
ENSG00000131469	chromatin interactions

Extended variants
information (count: 1515 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1515 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2305517	chrX:154774663-154774664	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112281020	chrX:154774689-154774690	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs201707101	chrX:154774706-154774707	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs2305518	chrX:154774707-154774708	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs200155488	chrX:154774750-154774751	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs141971703	chrX:154774761-154774762	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs368225710	chrX:154774838-154774839	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
8	rs145732983	chrX:154774864-154774865	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
9	rs34214712	chrX:154774866-154774867	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
10	rs191703052	chrX:154774979-154774980	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs372832403	chrX:154774982-154774983	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs375838964	chrX:154774987-154774988	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs78958682	chrX:154775077-154775078	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs181906527	chrX:154775123-154775124	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs12011310	chrX:154775251-154775252	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs5940476	chrX:154775278-154775279	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs186077403	chrX:154775305-154775306	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs148470394	chrX:154775343-154775344	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs189902449	chrX:154775435-154775436	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs5940477	chrX:154775452-154775453	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs370481709	chrX:154775540-154775541	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs182175124	chrX:154775604-154775605	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7051919	chrX:154775711-154775712	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs191089814	chrX:154775892-154775893	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs183156323	chrX:154775936-154775937	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs151240263	chrX:154776186-154776187	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs188431996	chrX:154776188-154776189	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs5940478	chrX:154776197-154776198	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs5983720	chrX:154776253-154776254	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs5940376	chrX:154776510-154776511	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs5940479	chrX:154776644-154776645	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs5940480	chrX:154776650-154776651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374526986	chrX:154776700-154776701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78653902	chrX:154776722-154776723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191988264	chrX:154776836-154776837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs5940481	chrX:154776845-154776846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34526207	chrX:154776856-154776857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs5940482	chrX:154776866-154776867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs5940377	chrX:154776869-154776870	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
40	rs371060480	chrX:154776899-154776900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs5983721	chrX:154776906-154776907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112744578	chrX:154776930-154776931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5940378	chrX:154776951-154776952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs5940379	chrX:154776954-154776955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs5940483	chrX:154776957-154776958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368403544	chrX:154777041-154777042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184243092	chrX:154777047-154777048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111592891	chrX:154777055-154777056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7878725	chrX:154777063-154777064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192741092	chrX:154777089-154777090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
lymphocytic leukemia	21291569	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
Cancer	16751803	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
abnormal development	18461090	CNVD
Premature ovarian failure	20952765	CNVD
Abnormal corpus callosum	21572526	CNVD
Breast cancer	21364760	CNVD
Astrocytoma	22246337	CNVD
Cerebellar atrophy	21569638	CNVD
periventricular nodular heterotopia	21572526	CNVD
Cerebellar hypoplasia	21569638	CNVD
Hoyeraal-Hreidarsson syndrome	21569638	CNVD
Oto-palato-digital type II	21569638	CNVD
incontinentia pigmenti anhidrotic ectodermal dysplasia with immunodeficiency	18350553	CNVD
Aqueductal stenosis	21572526	CNVD
Hirschsprung''s Disease	21712996	CNVD
Vermis hypoplasia	21569638	CNVD
X-linked hydrocephalus	21569638	CNVD
Rett syndrome	21569638	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	20970697	CNVD
Epilepsy	20970697	CNVD
Hemophilia A	17823971	CNVD
Rett syndrome	18923514	CNVD
Rett syndrome	22241247	CNVD
Intellectual disability	21984752	CNVD
Mental retardation	19951919	CNVD
Hypotonia	17088400	CNVD
Intellectual disability	22511893	CNVD
Mental retardation	17088400	CNVD
Mental retardation	21119712	CNVD
Neurodevelopmental disorder	19324899	CNVD
Recurrent Infections	17088400	CNVD
Rett syndrome	22283845	CNVD
Rett syndrome	21383316	CNVD
Cryptorchidism	21048976	CNVD
Disorders of sex development	21048976	CNVD
Cervical cancer	21062161	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Hemophilia A	18787571	CNVD
Hunters syndrom	18787571	CNVD
Prader-willi syndrome	20588305	CNVD
Mental retardation	19057379	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
abortions and stillbirths	19751515	CNVD
Hereditary coagulopathy	21993689	CNVD
Intellectual disability	23615299	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154734600-154777000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chrX:154739800-154775200	Weak transcription	HSMM	muscle
3	chrX:154752400-154776400	Weak transcription	Psoas Muscle	Psoas
4	chrX:154752400-154776600	Weak transcription	Fetal Heart	heart
5	chrX:154756200-154777000	Weak transcription	Left Ventricle	heart
6	chrX:154757000-154785800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chrX:154764800-154776800	Weak transcription	K562	blood
8	chrX:154766200-154776000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chrX:154767400-154775600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chrX:154771000-154775200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chrX:154771800-154776400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chrX:154771800-154776400	Weak transcription	Brain Anterior Caudate	brain
13	chrX:154772000-154775000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chrX:154772000-154775000	ZNF genes & repeats	Fetal Muscle Leg	muscle
15	chrX:154772200-154774800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chrX:154772200-154775800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chrX:154772200-154777200	Weak transcription	Stomach Smooth Muscle	stomach
18	chrX:154772400-154774800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chrX:154772400-154775000	Strong transcription	Primary T cells fromperipheralblood	blood
20	chrX:154772400-154775600	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chrX:154772400-154778000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chrX:154772800-154775400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chrX:154772800-154776000	Weak transcription	Placenta	Placenta
24	chrX:154773000-154775000	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chrX:154773000-154775000	Strong transcription	Fetal Intestine Large	intestine
26	chrX:154773000-154775200	ZNF genes & repeats	Primary T cells from cord blood	blood
27	chrX:154773000-154775600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chrX:154773000-154775600	Weak transcription	Thymus	Thymus
29	chrX:154773200-154774800	Strong transcription	Duodenum Mucosa	Duodenum
30	chrX:154773200-154774800	Strong transcription	Skeletal Muscle Female	skeletal muscle
31	chrX:154773200-154775000	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chrX:154773200-154775600	Weak transcription	Fetal Thymus	thymus
33	chrX:154773400-154775000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chrX:154773400-154775000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chrX:154773400-154775000	Strong transcription	Ovary	ovary
36	chrX:154773400-154776400	Strong transcription	Primary hematopoietic stem cells	blood
37	chrX:154773600-154774800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
38	chrX:154773600-154774800	Strong transcription	Brain Germinal Matrix	brain
39	chrX:154773600-154775000	Strong transcription	Fetal Lung	lung
40	chrX:154773600-154775400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chrX:154773600-154775800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chrX:154773800-154774800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
43	chrX:154773800-154774800	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chrX:154773800-154775000	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chrX:154773800-154775000	Weak transcription	GM12878-XiMat	blood
46	chrX:154773800-154775400	Strong transcription	Dnd41	blood
47	chrX:154773800-154776400	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chrX:154773800-154787000	Weak transcription	Brain Angular Gyrus	brain
49	chrX:154774000-154774800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chrX:154774000-154776000	Weak transcription	Rectal Mucosa Donor 31	rectum

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