Variant report

Variant	esv3391838
Chromosome Location	chrX:57144560-57160412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:495)
CpG islands
(count:611)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:57148014-57148186	K562	blood:	n/a	n/a
2	ARID3A	chrX:57147912-57148112	HepG2	liver:	n/a	n/a
3	BCLAF1	chrX:57147792-57148176	GM12878	blood:	n/a	chrX:57147863-57147876
4	BHLHE40	chrX:57147564-57147802	A549	lung:	n/a	chrX:57147702-57147715 chrX:57147705-57147714 chrX:57147767-57147783 chrX:57147704-57147713 chrX:57147704-57147713 chrX:57147698-57147719
5	BHLHE40	chrX:57147402-57148124	HepG2	liver:	n/a	chrX:57147702-57147715 chrX:57147705-57147714 chrX:57147767-57147783 chrX:57147704-57147713 chrX:57147704-57147713 chrX:57147698-57147719
6	BHLHE40	chrX:57147528-57148199	GM12878	blood:	n/a	chrX:57147702-57147715 chrX:57147705-57147714 chrX:57147767-57147783 chrX:57147704-57147713 chrX:57147704-57147713 chrX:57147698-57147719
7	BHLHE40	chrX:57145985-57145998	GM12878	blood:	n/a	n/a
8	BHLHE40	chrX:57147524-57148211	K562	blood:	n/a	chrX:57147702-57147715 chrX:57147705-57147714 chrX:57147767-57147783 chrX:57147704-57147713 chrX:57147704-57147713 chrX:57147698-57147719
9	BRCA1	chrX:57148000-57148162	HepG2	liver:	n/a	n/a
10	CEBPB	chrX:57158950-57159160	K562	blood:	n/a	n/a
11	CEBPB	chrX:57159664-57159814	IMR90	lung:	n/a	n/a
12	CEBPD	chrX:57147961-57148214	HepG2	liver:	n/a	n/a
13	CHD1	chrX:57147781-57147795	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chrX:57148588-57148788	GM12878	blood:	n/a	n/a
15	CHD1	chrX:57147751-57147977	GM12878	blood:	n/a	n/a
16	CHD2	chrX:57147546-57148211	GM12878	blood:	n/a	n/a
17	CHD2	chrX:57147446-57148055	HepG2	liver:	n/a	n/a
18	CHD2	chrX:57147392-57148201	Hela-S3	cervix:	n/a	n/a
19	CHD2	chrX:57147701-57147805	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chrX:57147677-57147936	K562	blood:	n/a	n/a
21	CREB1	chrX:57147842-57148225	A549	lung:	n/a	n/a
22	CTCF	chrX:57147537-57147768	IMR90	lung:	n/a	chrX:57147650-57147666
23	CTCF	chrX:57147604-57147796	GM10248	blood:	n/a	chrX:57147650-57147666
24	CTCF	chrX:57147636-57147786	Lung_OC	lung:	n/a	chrX:57147650-57147666
25	CTCF	chrX:57145416-57145504	LNCaP	prostate:	n/a	n/a
26	CTCF	chrX:57147640-57147790	HepG2	liver:	n/a	chrX:57147650-57147666
27	CTCF	chrX:57147720-57147870	GM12866	blood:	n/a	n/a
28	CTCF	chrX:57147680-57147830	HPAF	blood vessel:	n/a	n/a
29	CTCF	chrX:57147553-57147775	Hela-S3	cervix:	n/a	chrX:57147650-57147666
30	CTCF	chrX:57147820-57147916	MCF-7	breast:	n/a	n/a
31	CTCF	chrX:57147842-57147897	GM12892	blood:	n/a	n/a
32	CTCF	chrX:57144889-57144913	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chrX:57147574-57147771	GM20000	blood:	n/a	chrX:57147650-57147666
34	CTCF	chrX:57147720-57147870	HPAF	blood vessel:	n/a	n/a
35	CTCF	chrX:57147680-57147830	HRPEpiC	eye:	n/a	n/a
36	CTCF	chrX:57147660-57147810	HRE	kidney:	n/a	n/a
37	CTCF	chrX:57147918-57147923	MCF-7	breast:	n/a	n/a
38	CTCF	chrX:57147720-57147870	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chrX:57147720-57147870	HepG2	liver:	n/a	n/a
40	CTCF	chrX:57147720-57147870	BJ	skin:	n/a	n/a
41	CTCF	chrX:57147720-57147870	GM12868	blood:	n/a	n/a
42	CTCF	chrX:57147820-57147970	GM12865	blood:	n/a	n/a
43	CTCF	chrX:57147557-57147765	MCF-7	breast:	n/a	chrX:57147650-57147666
44	CTCF	chrX:57147560-57147801	H1-hESC	embryonic stem cell:	n/a	chrX:57147650-57147666
45	CTCF	chrX:57147739-57148022	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chrX:57157050-57157102	HepG2	liver:	n/a	n/a
47	CTCF	chrX:57147552-57147816	MCF-7	breast:	n/a	chrX:57147650-57147666
48	CTCF	chrX:57147700-57147850	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chrX:57147660-57147810	GM12870	blood:	n/a	n/a
50	CTCF	chrX:57147420-57147570	SK-N-SH_RA	brain:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:57148068-57148118	Hela-S3	cervix:	n/a
2	chrX:57148068-57148118	Hela-S3	cervix:	n/a
3	chrX:57148116-57148166	HUVEC	blood vessel:	n/a
4	chrX:57148068-57148118	ovcar-3	ovarian:	n/a
5	chrX:57147699-57147749	CMK	blood:	n/a
6	chrX:57147697-57147747	LNCaP	prostate:	n/a
7	chrX:57147697-57147747	Caco-2	colon:	n/a
8	chrX:57148257-57148307	A549	lung:	n/a
9	chrX:57145316-57145366	HAEpiC	amniotic membrane:	n/a
10	chrX:57148068-57148118	HepG2	liver:	n/a
11	chrX:57147699-57147749	BJ	skin:	n/a
12	chrX:57147699-57147749	HRPEpiC	eye:	n/a
13	chrX:57148068-57148118	Hepatocyte	liver:	n/a
14	chrX:57147872-57147922	HepG2	liver:	n/a
15	chrX:57145316-57145366	GM12878	blood:	n/a
16	chrX:57148257-57148307	BJ	skin:	n/a
17	chrX:57148116-57148166	AoSMC	blood vessel:	n/a
18	chrX:57147697-57147747	NHDF-neo	bronchial:	n/a
19	chrX:57151771-57151821	K562	blood:	n/a
20	chrX:57148257-57148307	MCF10A-Er-Src	breast:	n/a
21	chrX:57148068-57148118	NH-A	brain:	n/a
22	chrX:57148068-57148118	SAEC	small airway:	n/a
23	chrX:57147369-57147419	MCF-7	breast:	n/a
24	chrX:57151771-57151821	U87	brain:	n/a
25	chrX:57148068-57148118	HL-60	blood:	n/a
26	chrX:57148116-57148166	Hepatocyte	liver:	n/a
27	chrX:57147369-57147419	AG10803	skin:	n/a
28	chrX:57145316-57145366	HL-60	blood:	n/a
29	chrX:57147369-57147419	HCPEpiC	choroid plexus:	n/a
30	chrX:57148257-57148307	Jurkat	blood:	n/a
31	chrX:57148116-57148166	AG09319	gingival:	n/a
32	chrX:57147699-57147749	SK-N-MC	brain:	n/a
33	chrX:57147697-57147747	HEK293	kidney:	embryo
34	chrX:57147697-57147747	PrEC	prostate:	n/a
35	chrX:57145316-57145366	RPTEC	kidney:	n/a
36	chrX:57148116-57148166	GM06990	blood:	n/a
37	chrX:57148257-57148307	SK-N-SH_RA	brain:	n/a
38	chrX:57147918-57147968	PFSK-1	brain:	n/a
39	chrX:57147697-57147747	HUVEC	blood vessel:	n/a
40	chrX:57147918-57147968	BJ	skin:	n/a
41	chrX:57147699-57147749	PFSK-1	brain:	n/a
42	chrX:57147699-57147749	HEK293	kidney:	embryo
43	chrX:57148068-57148118	GM12878	blood:	n/a
44	chrX:57148257-57148307	GM12878	blood:	n/a
45	chrX:57148068-57148118	CMK	blood:	n/a
46	chrX:57151771-57151821	HRPEpiC	eye:	n/a
47	chrX:57151771-57151821	HPAEpiC	pulmonary alveolar:	n/a
48	chrX:57148257-57148307	Caco-2	colon:	n/a
49	chrX:57151771-57151821	HRE	kidney:	n/a
50	chrX:57145316-57145366	BJ	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:57147420..57149471-chrX:57153096..57155249,2	K562	blood:
2	chrX:57151959..57154469-chrX:57161082..57164031,2	K562	blood:
3	chrX:57148077..57149890-chrX:57150296..57152949,3	K562	blood:
4	chrX:57148077..57149890-chrX:57150631..57152949,2	K562	blood:
5	chr1:200638588..200639361-chrX:57147651..57148365,2	Hela-S3	cervix:
6	chrX:57153956..57156942-chrX:57158731..57161040,2	K562	blood:
7	chrX:56850607..56853538-chrX:57149099..57151794,2	K562	blood:
8	chrX:57147871..57149663-chrX:57158200..57160464,3	MCF-7	breast:
9	chrX:57153956..57156942-chrX:57158731..57161040,2	K562	blood:
10	chrX:57151889..57154645-chrX:57155969..57158302,2	MCF-7	breast:
11	chrX:57151889..57154645-chrX:57155969..57158302,2	MCF-7	breast:
12	chrX:57020514..57023354-chrX:57159798..57161801,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAAH2-2	chrX:57153318-57153676	XLOC_007996
2	lnc-FAAH2-2	chrX:57148042-57148400	NONHSAT137282
3	lnc-FAAH2-2	chrX:57148380-57148400	XLOC_007996
4	lnc-FAAH2-2	chrX:57153318-57153491	XLOC_007996
5	lnc-FAAH2-2	chrX:57148095-57148400	XLOC_007996
6	lnc-FAAH2-2	chrX:57153319-57154636	NONHSAT137282
7	lnc-FAAH2-2	chrX:57154177-57154235	XLOC_007996

No data

Variant related genes	Relation type
ENSG00000226310	TF binding region
SPIN2B	TF binding region
ENSG00000226310	CpG island
SPIN2B	CpG island
ENSG00000204271	chromatin interactions
ENSG00000226310	chromatin interactions
ENSG00000147059	chromatin interactions
ENSG00000260088	chromatin interactions
ENSG00000118197	chromatin interactions
ENSG00000186787	chromatin interactions
PPP1R14C	miRNA target sites
C17orf68	miRNA target sites
RNF19A	miRNA target sites

Extended variants
information (count: 189 )
Associated
traits (count: 40 )

Variant overlapped rSNPs/rCNVs (count:189 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs707344	chrX:57144649-57144650	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs190482284	chrX:57144670-57144671	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs182730724	chrX:57144676-57144677	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs186405928	chrX:57144683-57144684	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs571561195	chrX:57144748-57144749	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs191091806	chrX:57144791-57144792	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs377148477	chrX:57144826-57144827	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs144697603	chrX:57144870-57144871	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs112982350	chrX:57144885-57144886	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs148688442	chrX:57144968-57144969	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs408297	chrX:57144970-57144971	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs41307629	chrX:57145079-57145080	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538962042	chrX:57145224-57145225	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs187564510	chrX:57145327-57145328	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs193297778	chrX:57145345-57145346	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs369908446	chrX:57145455-57145456	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs183066435	chrX:57145530-57145531	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs142244268	chrX:57145585-57145586	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs187398309	chrX:57145627-57145628	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs436217	chrX:57145643-57145644	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs409085	chrX:57145996-57145997	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs147850709	chrX:57146032-57146033	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs707345	chrX:57146035-57146036	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs1736864	chrX:57146122-57146123	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs1736863	chrX:57146123-57146124	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs1736862	chrX:57146129-57146130	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs11547403	chrX:57146131-57146132	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs364007	chrX:57146205-57146206	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs370748637	chrX:57146262-57146263	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs199979060	chrX:57146263-57146264	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs201180740	chrX:57146865-57146866	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs201872206	chrX:57146927-57146928	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs200446826	chrX:57146931-57146932	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs201521097	chrX:57146945-57146946	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs550578586	chrX:57147215-57147216	Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs7055254	chrX:57147244-57147245	Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs568850935	chrX:57147681-57147682	Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs73494640	chrX:57147733-57147734	Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs432644	chrX:57147883-57147884	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs2071722	chrX:57147944-57147945	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs376510480	chrX:57148178-57148179	Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs369194312	chrX:57148301-57148302	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs372783829	chrX:57148308-57148309	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs184270409	chrX:57148323-57148324	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs5960904	chrX:57148607-57148608	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs188412875	chrX:57148735-57148736	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs192684119	chrX:57148845-57148846	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs707346	chrX:57148894-57148895	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs184678304	chrX:57149011-57149012	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs188991390	chrX:57149021-57149022	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:40)

Disease	PMID	Source
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
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	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
Thyroid cancer	19087340	CNVD
lymphocytic leukemia	21291569	CNVD
Cervical cancer	21062161	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	19835627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:57107800-57147200	Weak transcription	Right Ventricle	heart
2	chrX:57108400-57147200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chrX:57109400-57147200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chrX:57116200-57147200	Weak transcription	HSMM	muscle
5	chrX:57117000-57147800	Weak transcription	Primary B cells from cord blood	blood
6	chrX:57117600-57147200	Weak transcription	Spleen	Spleen
7	chrX:57118600-57147200	Weak transcription	Thymus	Thymus
8	chrX:57119600-57147200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chrX:57119600-57147200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chrX:57119800-57147400	Weak transcription	Aorta	Aorta
11	chrX:57120000-57147200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chrX:57121600-57147200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chrX:57121800-57147200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chrX:57121800-57147200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chrX:57122000-57147200	Weak transcription	Fetal Intestine Small	intestine
16	chrX:57122000-57147200	Weak transcription	Left Ventricle	heart
17	chrX:57122000-57147200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chrX:57122000-57147400	Weak transcription	Placenta Amnion	Placenta Amnion
19	chrX:57122000-57147400	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chrX:57122000-57147400	Weak transcription	Small Intestine	intestine
21	chrX:57122200-57147400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chrX:57122400-57144600	Weak transcription	Fetal Intestine Large	intestine
23	chrX:57122600-57147200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chrX:57126000-57147200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chrX:57127200-57145800	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chrX:57128000-57147400	Weak transcription	Primary B cells from peripheral blood	blood
27	chrX:57131000-57147200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chrX:57131600-57147200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chrX:57132800-57147200	Weak transcription	NH-A	brain
30	chrX:57133200-57147200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chrX:57133200-57147200	Weak transcription	NHLF	lung
32	chrX:57133400-57147200	Weak transcription	Fetal Thymus	thymus
33	chrX:57134000-57147200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chrX:57134000-57147200	Weak transcription	Pancreas	Pancrea
35	chrX:57134200-57145200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chrX:57134200-57147200	Weak transcription	Fetal Brain Female	brain
37	chrX:57134600-57147200	Weak transcription	Osteobl	bone
38	chrX:57135000-57147200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chrX:57135200-57147200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chrX:57135200-57147200	Weak transcription	HSMMtube	muscle
41	chrX:57135600-57147200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chrX:57135600-57147200	Weak transcription	Adipose Nuclei	Adipose
43	chrX:57135800-57144600	Weak transcription	Fetal Stomach	stomach
44	chrX:57135800-57145200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chrX:57135800-57145600	Weak transcription	Dnd41	blood
46	chrX:57135800-57147200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chrX:57135800-57147200	Weak transcription	Ovary	ovary
48	chrX:57136000-57144800	Weak transcription	Primary hematopoietic stem cells	blood
49	chrX:57136000-57145200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chrX:57136600-57147200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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