Variant report

Variant	nsv818043
Chromosome Location	chrX:154737376-154777564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:110)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:110 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chrX:154755950-154756274	K562	blood:	n/a	n/a
2	CTCF	chrX:154764540-154764690	MCF-7	breast:	n/a	n/a
3	CTCF	chrX:154764600-154764750	HPAF	blood vessel:	n/a	n/a
4	CTCF	chrX:154764547-154764822	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chrX:154764606-154764741	GM12878	blood:	n/a	n/a
6	CTCF	chrX:154764605-154764704	LNCaP	prostate:	n/a	n/a
7	CTCF	chrX:154764580-154764730	HEK293	kidney:	n/a	n/a
8	CTCF	chrX:154764623-154764741	MCF-7	breast:	n/a	n/a
9	CTCF	chrX:154764638-154764730	GM12892	blood:	n/a	n/a
10	CTCF	chrX:154764560-154764710	HMEC	breast:	n/a	n/a
11	CTCF	chrX:154764562-154764719	Hela-S3	cervix:	n/a	n/a
12	CTCF	chrX:154764540-154764690	K562	blood:	n/a	n/a
13	CTCF	chrX:154764619-154764743	GM19240	blood:	n/a	n/a
14	CTCF	chrX:154764607-154764664	Spleen_OC	spleen:	n/a	n/a
15	CTCF	chrX:154764566-154764738	MCF-7	breast:	n/a	n/a
16	CTCF	chrX:154764632-154764703	GM19238	blood:	n/a	n/a
17	CTCF	chrX:154764551-154764749	K562	blood:	n/a	n/a
18	CTCF	chrX:154764601-154764703	HepG2	liver:	n/a	n/a
19	CTCF	chrX:154764545-154764756	MCF-7	breast:	n/a	n/a
20	CTCF	chrX:154764600-154764750	GM12869	blood:	n/a	n/a
21	CTCF	chrX:154764642-154764718	A549	lung:	n/a	n/a
22	CTCF	chrX:154764646-154764662	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chrX:154764551-154764738	HepG2	liver:	n/a	n/a
24	CTCF	chrX:154764500-154764830	K562	blood:	n/a	n/a
25	CTCF	chrX:154764477-154764791	GM12878	blood:	n/a	n/a
26	CTCF	chrX:154764607-154764684	GM10248	blood:	n/a	n/a
27	CTCF	chrX:154764448-154764846	K562	blood:	n/a	n/a
28	CTCF	chrX:154764520-154764670	Caco-2	colon:	n/a	n/a
29	CTCF	chrX:154764600-154764750	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chrX:154764560-154764710	GM12873	blood:	n/a	n/a
31	CTCF	chrX:154764487-154764771	A549	lung:	n/a	n/a
32	CTCF	chrX:154764600-154764750	A549	lung:	n/a	n/a
33	CTCF	chrX:154764444-154764779	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chrX:154764457-154764892	HCT-116	colon:	n/a	n/a
35	CTCF	chrX:154741049-154741115	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chrX:154764507-154764789	K562	blood:	n/a	n/a
37	CTCF	chrX:154764619-154764675	GM13977	blood:	n/a	n/a
38	CTCF	chrX:154764324-154764994	A549	lung:	n/a	n/a
39	CTCF	chrX:154764545-154764749	A549	lung:	n/a	n/a
40	CTCF	chrX:154764477-154764846	MCF-7	breast:	n/a	n/a
41	CTCF	chrX:154764580-154764730	GM06990	blood:	n/a	n/a
42	CTCF	chrX:154764499-154764842	MCF-7	breast:	n/a	n/a
43	CTCF	chrX:154764480-154764630	HMEC	breast:	n/a	n/a
44	CTCF	chrX:154764560-154764710	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chrX:154764620-154764770	MCF-7	breast:	n/a	n/a
46	CTCF	chrX:154764469-154764869	K562	blood:	n/a	n/a
47	CUX1	chrX:154739027-154739376	K562	blood:	n/a	n/a
48	E2F4	chrX:154759846-154760025	MCF10A-Er-Src	breast:	n/a	n/a
49	EP300	chrX:154769380-154769398	GM12878	blood:	n/a	n/a
50	FOS	chrX:154765578-154765903	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:154769629-154769679	NHDF-neo	bronchial:	n/a
2	chrX:154769629-154769679	ECC-1	luminal epithelium:	n/a
3	chrX:154769629-154769679	HEK293	kidney:	embryo
4	chrX:154769629-154769679	MCF10A-Er-Src	breast:	n/a
5	chrX:154769629-154769679	GM19239	blood:	n/a
6	chrX:154769629-154769679	HCT-116	colon:	n/a
7	chrX:154769629-154769679	SK-N-SH	brain:	n/a
8	chrX:154769629-154769679	LNCaP	prostate:	n/a
9	chrX:154769629-154769679	HCPEpiC	choroid plexus:	n/a
10	chrX:154769629-154769679	HRPEpiC	eye:	n/a
11	chrX:154769629-154769679	RPTEC	kidney:	n/a
12	chrX:154769629-154769679	GM12892	blood:	n/a
13	chrX:154769629-154769679	AG09309	skin:	n/a
14	chrX:154769629-154769679	AG04450	lung:	fetal
15	chrX:154769629-154769679	HRE	kidney:	n/a
16	chrX:154769629-154769679	HUVEC	blood vessel:	n/a
17	chrX:154769629-154769679	SAEC	small airway:	n/a
18	chrX:154769629-154769679	ovcar-3	ovarian:	n/a
19	chrX:154769629-154769679	SKMC	muscle:	n/a
20	chrX:154769629-154769679	CMK	blood:	n/a
21	chrX:154769629-154769679	Hepatocyte	liver:	n/a
22	chrX:154769629-154769679	HepG2	liver:	n/a
23	chrX:154769629-154769679	AG04449	skin:	fetal
24	chrX:154769629-154769679	HL-60	blood:	n/a
25	chrX:154769629-154769679	Hela-S3	cervix:	n/a
26	chrX:154769629-154769679	HRCEpiC	kidney:	n/a
27	chrX:154769629-154769679	AG10803	skin:	n/a
28	chrX:154769629-154769679	GM12891	blood:	n/a
29	chrX:154769629-154769679	Jurkat	blood:	n/a
30	chrX:154769629-154769679	MCF-7	breast:	n/a
31	chrX:154769629-154769679	A549	lung:	n/a
32	chrX:154769629-154769679	BJ	skin:	n/a
33	chrX:154769629-154769679	NB4	blood:	n/a
34	chrX:154769629-154769679	PrEC	prostate:	n/a
35	chrX:154769629-154769679	GM06990	blood:	n/a
36	chrX:154769629-154769679	HMEC	breast:	n/a
37	chrX:154769629-154769679	NT2-D1	testis:	n/a
38	chrX:154769629-154769679	Caco-2	colon:	n/a
39	chrX:154769629-154769679	U87	brain:	n/a
40	chrX:154769629-154769679	NHBE	bronchial:	n/a
41	chrX:154769629-154769679	HNPCEpiC	eye:	n/a
42	chrX:154769629-154769679	NH-A	brain:	n/a
43	chrX:154769629-154769679	ProgFib	skin:	n/a
44	chrX:154769629-154769679	AG09319	gingival:	n/a
45	chrX:154769629-154769679	SK-N-SH_RA	brain:	n/a
46	chrX:154769629-154769679	HCF	heart:	n/a
47	chrX:154769629-154769679	HEEpiC	esophagus:	n/a
48	chrX:154769629-154769679	HPAEpiC	pulmonary alveolar:	n/a
49	chrX:154769629-154769679	SK-N-MC	brain:	n/a
50	chrX:154769629-154769679	IMR90	lung:	fetal

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:154736584..154738265-chrX:154744068..154745835,2	K562	blood:
2	chrX:154764181..154765520-chrX:154880551..154881570,5	MCF-7	breast:
3	chrX:154736584..154738265-chrX:154744068..154745835,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F8A2-3	chrX:154739490-154739868	NONHSAT139242
2	lnc-TMLHE-2	chrX:154774828-154774938	NONHSAT139243

No data

Variant related genes	Relation type
TMLHE	TF binding region
TMLHE	CpG island

Extended variants
information (count: 534 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5940372	chrX:154737376-154737377	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185683009	chrX:154737426-154737427	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146839237	chrX:154737440-154737441	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370020879	chrX:154737519-154737520	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190642126	chrX:154737799-154737800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139776043	chrX:154737833-154737834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182881574	chrX:154738054-154738055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144493076	chrX:154738176-154738177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187951530	chrX:154738254-154738255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144914944	chrX:154738301-154738302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193044865	chrX:154738376-154738377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149032698	chrX:154738378-154738379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142036772	chrX:154738401-154738402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35317427	chrX:154738410-154738411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151171578	chrX:154738453-154738454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377320148	chrX:154738721-154738722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183971306	chrX:154738819-154738820	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141192145	chrX:154738898-154738899	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187715182	chrX:154739002-154739003	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs192692173	chrX:154739028-154739029	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs989711	chrX:154739500-154739501	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs184155727	chrX:154739719-154739720	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
23	rs376124147	chrX:154739757-154739758	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs188369069	chrX:154739791-154739792	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
25	rs372008648	chrX:154739880-154739881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370981833	chrX:154739893-154739894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376914267	chrX:154739894-154739895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs5940459	chrX:154739926-154739927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200117820	chrX:154739929-154739930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79920288	chrX:154740179-154740180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs76536573	chrX:154740180-154740181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373222538	chrX:154740245-154740246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12928758	chrX:154740309-154740310	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12378859	chrX:154740363-154740364	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs10007922	chrX:154740372-154740373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7055784	chrX:154740386-154740387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs5940460	chrX:154740429-154740430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112972622	chrX:154740480-154740481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs5940461	chrX:154740552-154740553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373813291	chrX:154740596-154740597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367623112	chrX:154740612-154740613	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs113785662	chrX:154740663-154740664	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs112229096	chrX:154740678-154740679	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs150163698	chrX:154740682-154740683	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs190732390	chrX:154740804-154740805	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs182239784	chrX:154740868-154740869	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs187337890	chrX:154740942-154740943	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs138177678	chrX:154740953-154740954	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs189349813	chrX:154740980-154740981	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs367747960	chrX:154740984-154740985	Weak transcription Strong transcription ZNF genes & repeats	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	21293372	CNVD

Chromatin state (count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154732600-154751800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chrX:154732600-154751800	Weak transcription	Brain Hippocampus Middle	brain
3	chrX:154732800-154739200	Weak transcription	Fetal Lung	lung
4	chrX:154732800-154739400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chrX:154732800-154740800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chrX:154732800-154740800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chrX:154732800-154751600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chrX:154732800-154752000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chrX:154732800-154752000	Weak transcription	Duodenum Mucosa	Duodenum
10	chrX:154733000-154742400	Weak transcription	A549	lung
11	chrX:154733200-154739600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chrX:154733400-154752000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chrX:154733600-154739200	Weak transcription	Primary B cells from cord blood	blood
14	chrX:154733600-154740800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chrX:154733600-154740800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chrX:154733800-154740800	Weak transcription	Primary T cells from cord blood	blood
17	chrX:154733800-154740800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chrX:154733800-154752000	Weak transcription	Brain Germinal Matrix	brain
19	chrX:154734000-154737400	Weak transcription	Primary B cells from peripheral blood	blood
20	chrX:154734000-154738600	Weak transcription	Fetal Muscle Leg	muscle
21	chrX:154734000-154738800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chrX:154734000-154752000	Weak transcription	Placenta	Placenta
23	chrX:154734000-154754800	Weak transcription	Stomach Smooth Muscle	stomach
24	chrX:154734200-154737400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chrX:154734200-154740800	Weak transcription	Ovary	ovary
26	chrX:154734200-154740800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chrX:154734400-154739400	Weak transcription	Primary T cells fromperipheralblood	blood
28	chrX:154734400-154742400	Weak transcription	K562	blood
29	chrX:154734400-154755800	Weak transcription	Thymus	Thymus
30	chrX:154734600-154742200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chrX:154734600-154757200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chrX:154734600-154777000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chrX:154735000-154743000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chrX:154735000-154752000	Weak transcription	Brain Anterior Caudate	brain
35	chrX:154735200-154740800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chrX:154735200-154740800	Weak transcription	Liver	Liver
37	chrX:154735200-154742400	Weak transcription	Brain Cingulate Gyrus	brain
38	chrX:154735200-154752000	Weak transcription	Fetal Thymus	thymus
39	chrX:154735200-154754000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chrX:154735200-154755200	Weak transcription	Rectal Smooth Muscle	rectum
41	chrX:154735400-154740800	Weak transcription	Left Ventricle	heart
42	chrX:154735400-154740800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chrX:154735400-154754800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chrX:154735400-154773800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chrX:154735600-154737800	Strong transcription	Fetal Intestine Large	intestine
46	chrX:154735600-154742400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chrX:154735800-154752000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chrX:154736000-154740800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chrX:154736000-154742200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chrX:154736200-154738800	Weak transcription	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links