Variant report

Variant	nsv532913
Chromosome Location	chrX:122603383-122723979
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:608)
CpG islands
(count:549)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chrX:122611580-122611952	K562	blood:	n/a	n/a
2	BACH1	chrX:122608969-122609569	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chrX:122609166-122609570	K562	blood:	n/a	n/a
4	BACH1	chrX:122611934-122611957	K562	blood:	n/a	n/a
5	BATF	chrX:122658976-122659469	GM12878	blood:	n/a	n/a
6	BATF	chrX:122648332-122648512	GM12878	blood:	n/a	n/a
7	BCL11A	chrX:122648476-122648767	GM12878	blood:	n/a	n/a
8	BHLHE40	chrX:122659222-122659442	GM12878	blood:	n/a	n/a
9	BHLHE40	chrX:122647660-122647795	K562	blood:	n/a	n/a
10	BHLHE40	chrX:122648338-122648504	K562	blood:	n/a	n/a
11	CBX3	chrX:122648232-122648475	K562	blood:	n/a	n/a
12	CBX3	chrX:122672011-122672327	K562	blood:	n/a	n/a
13	CBX3	chrX:122648090-122648524	HCT-116	colon:	n/a	n/a
14	CBX3	chrX:122648030-122648590	K562	blood:	n/a	n/a
15	CCNT2	chrX:122648085-122648404	K562	blood:	n/a	n/a
16	CEBPB	chrX:122616356-122616674	K562	blood:	n/a	chrX:122616488-122616501 chrX:122616490-122616501
17	CEBPB	chrX:122703799-122704297	MCF-7	breast:	n/a	n/a
18	CEBPB	chrX:122723917-122724286	IMR90	lung:	n/a	chrX:122724092-122724103
19	CEBPB	chrX:122623071-122623231	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chrX:122723944-122724259	A549	lung:	n/a	chrX:122724092-122724103
21	CEBPB	chrX:122616311-122616681	IMR90	lung:	n/a	chrX:122616488-122616501 chrX:122616490-122616501
22	CEBPB	chrX:122611595-122611747	K562	blood:	n/a	n/a
23	CEBPB	chrX:122674674-122674989	HepG2	liver:	n/a	chrX:122674821-122674832 chrX:122674822-122674833
24	CEBPB	chrX:122723924-122724277	Hela-S3	cervix:	n/a	chrX:122724092-122724103
25	CEBPB	chrX:122690674-122690911	IMR90	lung:	n/a	n/a
26	CEBPB	chrX:122674696-122674931	K562	blood:	n/a	chrX:122674821-122674832 chrX:122674822-122674833
27	CEBPB	chrX:122703733-122704291	MCF-7	breast:	n/a	n/a
28	CEBPB	chrX:122680389-122680705	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:122616331-122616633	Hela-S3	cervix:	n/a	chrX:122616488-122616501 chrX:122616490-122616501
30	CEBPB	chrX:122681819-122682019	K562	blood:	n/a	n/a
31	CEBPB	chrX:122723924-122724271	K562	blood:	n/a	chrX:122724092-122724103
32	CEBPB	chrX:122674704-122674926	IMR90	lung:	n/a	chrX:122674821-122674832 chrX:122674822-122674833
33	CEBPB	chrX:122723933-122724250	HepG2	liver:	n/a	chrX:122724092-122724103
34	CEBPB	chrX:122674702-122674975	Hela-S3	cervix:	n/a	chrX:122674821-122674832 chrX:122674822-122674833
35	CTCF	chrX:122615880-122616030	AG04450	lung:	n/a	n/a
36	CTCF	chrX:122633827-122633888	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chrX:122648243-122648677	A549	lung:	n/a	n/a
38	CTCF	chrX:122610780-122610930	MCF-7	breast:	n/a	chrX:122610869-122610877
39	CTCF	chrX:122610840-122610920	HepG2	liver:	n/a	chrX:122610869-122610877
40	CTCF	chrX:122681017-122681107	LNCaP	prostate:	n/a	n/a
41	CTCF	chrX:122648220-122648370	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chrX:122633739-122633819	GM12891	blood:	n/a	n/a
43	CTCF	chrX:122648410-122648470	GM20000	blood:	n/a	n/a
44	CTCF	chrX:122621014-122621080	ProgFib	skin:	n/a	n/a
45	CTCF	chrX:122615980-122616130	HRPEpiC	eye:	n/a	chrX:122616047-122616056 chrX:122616044-122616062 chrX:122616046-122616067
46	CTCF	chrX:122616000-122616150	NHDF-neo	bronchial:	n/a	chrX:122616047-122616056 chrX:122616044-122616062 chrX:122616046-122616067
47	CTCF	chrX:122678902-122679152	MCF-7	breast:	n/a	n/a
48	CTCF	chrX:122615940-122616090	HPAF	blood vessel:	n/a	chrX:122616047-122616056 chrX:122616044-122616062 chrX:122616046-122616067
49	CTCF	chrX:122637740-122637890	HEK293	kidney:	n/a	n/a
50	CTCF	chrX:122610765-122610899	ProgFib	skin:	n/a	chrX:122610869-122610877

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:122696318-122696368	NHDF-neo	bronchial:	n/a
2	chrX:122696026-122696076	HIPEpiC	eye:	n/a
3	chrX:122696417-122696467	HEEpiC	esophagus:	n/a
4	chrX:122696129-122696179	NT2-D1	testis:	n/a
5	chrX:122696026-122696076	HL-60	blood:	n/a
6	chrX:122696079-122696129	AG04450	lung:	fetal
7	chrX:122696318-122696368	NT2-D1	testis:	n/a
8	chrX:122696079-122696129	NB4	blood:	n/a
9	chrX:122696158-122696208	Caco-2	colon:	n/a
10	chrX:122696129-122696179	HepG2	liver:	n/a
11	chrX:122696026-122696076	AG04449	skin:	fetal
12	chrX:122624079-122624129	NHDF-neo	bronchial:	n/a
13	chrX:122696318-122696368	LNCaP	prostate:	n/a
14	chrX:122696254-122696304	ECC-1	luminal epithelium:	n/a
15	chrX:122696417-122696467	HCT-116	colon:	n/a
16	chrX:122696158-122696208	GM06990	blood:	n/a
17	chrX:122696254-122696304	PrEC	prostate:	n/a
18	chrX:122696026-122696076	K562	blood:	n/a
19	chrX:122696318-122696368	PrEC	prostate:	n/a
20	chrX:122696318-122696368	HL-60	blood:	n/a
21	chrX:122696417-122696467	HAEpiC	amniotic membrane:	n/a
22	chrX:122624079-122624129	HCM	heart:	n/a
23	chrX:122696158-122696208	HRCEpiC	kidney:	n/a
24	chrX:122696158-122696208	HIPEpiC	eye:	n/a
25	chrX:122696079-122696129	ovcar-3	ovarian:	n/a
26	chrX:122696406-122696456	HIPEpiC	eye:	n/a
27	chrX:122696254-122696304	RPTEC	kidney:	n/a
28	chrX:122696254-122696304	Caco-2	colon:	n/a
29	chrX:122624079-122624129	MCF10A-Er-Src	breast:	n/a
30	chrX:122696079-122696129	SK-N-MC	brain:	n/a
31	chrX:122696079-122696129	HCF	heart:	n/a
32	chrX:122696158-122696208	BE2_C	brain:	n/a
33	chrX:122624079-122624129	GM06990	blood:	n/a
34	chrX:122696406-122696456	RPTEC	kidney:	n/a
35	chrX:122696158-122696208	GM12892	blood:	n/a
36	chrX:122696417-122696467	HUVEC	blood vessel:	n/a
37	chrX:122696158-122696208	Hela-S3	cervix:	n/a
38	chrX:122696079-122696129	AG10803	skin:	n/a
39	chrX:122696129-122696179	SK-N-SH_RA	brain:	n/a
40	chrX:122696026-122696076	HAEpiC	amniotic membrane:	n/a
41	chrX:122696158-122696208	CMK	blood:	n/a
42	chrX:122696318-122696368	AG04449	skin:	fetal
43	chrX:122696318-122696368	HepG2	liver:	n/a
44	chrX:122696406-122696456	HRPEpiC	eye:	n/a
45	chrX:122696129-122696179	U87	brain:	n/a
46	chrX:122696079-122696129	HRE	kidney:	n/a
47	chrX:122696318-122696368	HCT-116	colon:	n/a
48	chrX:122696406-122696456	SK-N-SH_RA	brain:	n/a
49	chrX:122696158-122696208	MCF10A-Er-Src	breast:	n/a
50	chrX:122696079-122696129	HRPEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:122716034..122718337-chrX:122721169..122722949,2	MCF-7	breast:
2	chrX:122617368..122619467-chrX:122625173..122627505,2	K562	blood:
3	chrX:122597972..122599790-chrX:122611547..122613257,2	K562	blood:
4	chrX:122599051..122600959-chrX:122602705..122604634,2	MCF-7	breast:
5	chrX:122617368..122619835-chrX:122626005..122627948,2	K562	blood:
6	chrX:122618850..122621464-chrX:122644151..122646615,2	K562	blood:
7	chrX:122723340..122727763-chrX:122729541..122732093,5	K562	blood:
8	chrX:122610583..122612790-chrX:122647178..122648775,2	K562	blood:
9	chrX:122617368..122619467-chrX:122625173..122627505,2	K562	blood:
10	chrX:120964996..120967456-chrX:122628658..122631239,2	K562	blood:
11	chrX:122617368..122619835-chrX:122626005..122627948,2	K562	blood:
12	chrX:122716034..122718337-chrX:122721169..122722949,2	MCF-7	breast:
13	chrX:122617700..122619872-chrX:122633342..122635235,2	K562	blood:
14	chrX:122596493..122599360-chrX:122602327..122604363,3	K562	blood:
15	chrX:122618850..122621464-chrX:122644151..122646615,2	K562	blood:
16	chrX:122617700..122619872-chrX:122633342..122635235,2	K562	blood:
17	chrX:122644250..122646972-chrX:122648075..122649683,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRIA3-2	chrX:122692201-122692435	NONHSAT138421

No data

Variant related genes	Relation type
ENSG00000229733	TF binding region
GRIA3	TF binding region
ENSG00000179101	TF binding region
TUBB4AP1	TF binding region
ENSG00000229733	CpG island
GRIA3	CpG island
ENSG00000179101	CpG island
TUBB4AP1	CpG island
ENSG00000179101	chromatin interactions
ENSG00000265082	chromatin interactions

Extended variants
information (count: 1008 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187610339	chrX:122603431-122603432	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs57034498	chrX:122603463-122603464	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs151300076	chrX:122603524-122603525	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549930587	chrX:122603718-122603719	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs112710463	chrX:122603762-122603763	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112291381	chrX:122603812-122603813	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546332660	chrX:122604100-122604101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543706470	chrX:122604144-122604145	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190003758	chrX:122604226-122604227	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145684386	chrX:122604229-122604230	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547090439	chrX:122604296-122604297	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs58009413	chrX:122604426-122604427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182591381	chrX:122604431-122604432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551560598	chrX:122604446-122604447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555677864	chrX:122604561-122604562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369022408	chrX:122604705-122604706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141179752	chrX:122605147-122605148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187154616	chrX:122605225-122605226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144993923	chrX:122605338-122605339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376439620	chrX:122605436-122605437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149322654	chrX:122605523-122605524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191987639	chrX:122605543-122605544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374388538	chrX:122605648-122605649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184489893	chrX:122605752-122605753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs66626184	chrX:122605842-122605843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs5911626	chrX:122605986-122605987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574501104	chrX:122606421-122606422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148029697	chrX:122606551-122606552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73231103	chrX:122606718-122606719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374829211	chrX:122606741-122606742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147158871	chrX:122606963-122606964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs67159504	chrX:122606968-122606969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189009496	chrX:122607283-122607284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193105068	chrX:122607314-122607315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34471019	chrX:122607340-122607341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373495897	chrX:122607401-122607402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142675077	chrX:122607424-122607425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59687542	chrX:122607441-122607442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184256479	chrX:122607506-122607507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189255014	chrX:122607517-122607518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563120227	chrX:122607586-122607587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181139933	chrX:122607685-122607686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184103908	chrX:122607885-122607886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188862866	chrX:122607909-122607910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181572713	chrX:122607914-122607915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186799108	chrX:122607958-122607959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192102974	chrX:122607959-122607960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368265573	chrX:122607994-122607995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182217898	chrX:122608014-122608015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139065198	chrX:122608015-122608016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

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
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
lymphocytic leukemia	21291569	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
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21785460	CNVD
Astrocytoma	22246337	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Bladder cancer	24270882	CNVD
Breast cancer	17603634	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:122583800-122614200	Weak transcription	Brain Germinal Matrix	brain
2	chrX:122599000-122610400	Weak transcription	Brain Angular Gyrus	brain
3	chrX:122599400-122610000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chrX:122601000-122614800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chrX:122602000-122603600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chrX:122602000-122603800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chrX:122602600-122610000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chrX:122604400-122615200	Weak transcription	Fetal Brain Female	brain
9	chrX:122605000-122615400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chrX:122607000-122607400	Enhancers	HMEC	breast
11	chrX:122608600-122609400	Enhancers	GM12878-XiMat	blood
12	chrX:122609000-122609600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chrX:122609000-122609600	Enhancers	K562	blood
14	chrX:122609000-122609800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chrX:122609000-122610800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chrX:122609200-122610400	Enhancers	Fetal Lung	lung
17	chrX:122609400-122609600	Enhancers	Brain Cingulate Gyrus	brain
18	chrX:122609400-122611200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chrX:122609600-122614400	Weak transcription	Brain Cingulate Gyrus	brain
20	chrX:122610000-122610200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chrX:122610000-122610400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chrX:122610000-122610800	Enhancers	Colon Smooth Muscle	Colon
23	chrX:122610400-122611000	Enhancers	Brain Angular Gyrus	brain
24	chrX:122610400-122614000	Weak transcription	Fetal Lung	lung
25	chrX:122610600-122611000	Enhancers	Fetal Stomach	stomach
26	chrX:122610600-122611200	Enhancers	Pancreas	Pancrea
27	chrX:122610600-122611600	Enhancers	Rectal Smooth Muscle	rectum
28	chrX:122610800-122611200	Enhancers	Brain Substantia Nigra	brain
29	chrX:122610800-122613400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chrX:122611000-122613600	Weak transcription	Brain Angular Gyrus	brain
31	chrX:122611000-122616000	Weak transcription	Fetal Stomach	stomach
32	chrX:122611200-122611600	Weak transcription	Pancreas	Pancrea
33	chrX:122611400-122611800	Enhancers	Brain Substantia Nigra	brain
34	chrX:122611600-122612000	Enhancers	Pancreas	Pancrea
35	chrX:122611600-122615400	Weak transcription	Rectal Smooth Muscle	rectum
36	chrX:122613400-122613600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chrX:122613400-122614200	Enhancers	Fetal Brain Male	brain
38	chrX:122613400-122616800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chrX:122613600-122613800	Enhancers	Brain Angular Gyrus	brain
40	chrX:122613600-122614200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chrX:122613800-122614200	Weak transcription	Brain Angular Gyrus	brain
42	chrX:122614000-122614600	Enhancers	Fetal Lung	lung
43	chrX:122614000-122614800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chrX:122614000-122615800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chrX:122614200-122614400	Enhancers	Brain Angular Gyrus	brain
46	chrX:122614200-122615000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chrX:122614200-122615200	Enhancers	Brain Germinal Matrix	brain
48	chrX:122614200-122615200	Enhancers	Brain Hippocampus Middle	brain
49	chrX:122614400-122615000	Enhancers	Brain Cingulate Gyrus	brain
50	chrX:122614400-122616200	Weak transcription	Brain Angular Gyrus	brain

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