Variant report

Variant	esv2754822
Chromosome Location	chrX:80365094-80852865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2284)
CpG islands
(count:1037)
Chromatin interactive
region (count:43)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2284 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:80457189-80457610	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:80429861-80430140	HepG2	liver:	n/a	n/a
3	ATF2	chrX:80457057-80457822	GM12878	blood:	n/a	n/a
4	BACH1	chrX:80462558-80462719	K562	blood:	n/a	n/a
5	BACH1	chrX:80376864-80377364	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chrX:80664799-80664854	K562	blood:	n/a	n/a
7	BATF	chrX:80423923-80424180	GM12878	blood:	n/a	n/a
8	BHLHE40	chrX:80451289-80451478	GM12878	blood:	n/a	n/a
9	BHLHE40	chrX:80457238-80457671	GM12878	blood:	n/a	n/a
10	BHLHE40	chrX:80610953-80611111	K562	blood:	n/a	n/a
11	BHLHE40	chrX:80376424-80376605	K562	blood:	n/a	n/a
12	BHLHE40	chrX:80376499-80376667	GM12878	blood:	n/a	n/a
13	BHLHE40	chrX:80457473-80457688	K562	blood:	n/a	n/a
14	BRCA1	chrX:80377249-80377361	GM12878	blood:	n/a	n/a
15	BRCA1	chrX:80376863-80377587	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chrX:80457270-80457582	GM12878	blood:	n/a	n/a
17	BRCA1	chrX:80457064-80457740	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chrX:80457345-80457592	HepG2	liver:	n/a	n/a
19	BRCA1	chrX:80457817-80457819	GM12878	blood:	n/a	n/a
20	BRCA1	chrX:80457252-80457619	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chrX:80375504-80375785	Hela-S3	cervix:	n/a	n/a
22	CBX3	chrX:80799235-80799423	K562	blood:	n/a	n/a
23	CBX3	chrX:80799151-80799404	K562	blood:	n/a	n/a
24	CEBPB	chrX:80571803-80572082	IMR90	lung:	n/a	n/a
25	CEBPB	chrX:80372715-80372929	MCF-7	breast:	n/a	n/a
26	CEBPB	chrX:80634137-80634391	HepG2	liver:	n/a	chrX:80634227-80634238
27	CEBPB	chrX:80711850-80712194	IMR90	lung:	n/a	n/a
28	CEBPB	chrX:80372696-80372949	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chrX:80659742-80659999	IMR90	lung:	n/a	chrX:80659835-80659846 chrX:80659835-80659848
30	CEBPB	chrX:80457372-80457861	IMR90	lung:	n/a	n/a
31	CEBPB	chrX:80571784-80571971	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chrX:80388519-80388869	IMR90	lung:	n/a	n/a
33	CEBPB	chrX:80622157-80622473	HepG2	liver:	n/a	chrX:80622302-80622319
34	CEBPB	chrX:80784106-80784493	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chrX:80594431-80594816	IMR90	lung:	n/a	chrX:80594617-80594628
36	CEBPB	chrX:80460474-80460812	HepG2	liver:	n/a	chrX:80460640-80460651
37	CEBPB	chrX:80622211-80622490	A549	lung:	n/a	chrX:80622302-80622319
38	CEBPB	chrX:80571701-80572079	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chrX:80541502-80541932	MCF-7	breast:	n/a	n/a
40	CEBPB	chrX:80460496-80460826	K562	blood:	n/a	chrX:80460640-80460651
41	CEBPB	chrX:80417607-80417946	HepG2	liver:	n/a	chrX:80417772-80417783
42	CEBPB	chrX:80634108-80634374	A549	lung:	n/a	chrX:80634227-80634238
43	CEBPB	chrX:80463743-80464425	MCF-7	breast:	n/a	chrX:80463964-80463973 chrX:80463964-80463973 chrX:80463962-80463973 chrX:80463964-80463973 chrX:80463964-80463973
44	CEBPB	chrX:80460460-80460833	IMR90	lung:	n/a	chrX:80460640-80460651
45	CEBPB	chrX:80622147-80622482	IMR90	lung:	n/a	chrX:80622302-80622319
46	CEBPB	chrX:80388550-80388851	A549	lung:	n/a	n/a
47	CEBPB	chrX:80820323-80820564	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chrX:80659804-80660022	HepG2	liver:	n/a	chrX:80659835-80659846 chrX:80659835-80659848
49	CEBPB	chrX:80594443-80594802	HepG2	liver:	n/a	chrX:80594617-80594628
50	CEBPB	chrX:80366530-80366853	HepG2	liver:	n/a	chrX:80366684-80366695 chrX:80366534-80366551 chrX:80366686-80366695

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:80457015-80457065	AG09309	skin:	n/a
2	chrX:80457315-80457365	AoSMC	blood vessel:	n/a
3	chrX:80457709-80457759	AG09309	skin:	n/a
4	chrX:80458049-80458099	HPAEpiC	pulmonary alveolar:	n/a
5	chrX:80457442-80457492	HUVEC	blood vessel:	n/a
6	chrX:80457681-80457731	SK-N-MC	brain:	n/a
7	chrX:80457687-80457737	AG04450	lung:	fetal
8	chrX:80457567-80457617	NHDF-neo	bronchial:	n/a
9	chrX:80457960-80458010	HRE	kidney:	n/a
10	chrX:80457556-80457606	PrEC	prostate:	n/a
11	chrX:80457518-80457568	SAEC	small airway:	n/a
12	chrX:80457442-80457492	HCM	heart:	n/a
13	chrX:80457531-80457581	GM19239	blood:	n/a
14	chrX:80457315-80457365	AG09319	gingival:	n/a
15	chrX:80458049-80458099	HL-60	blood:	n/a
16	chrX:80457315-80457365	HUVEC	blood vessel:	n/a
17	chrX:80457681-80457731	AG09309	skin:	n/a
18	chrX:80376497-80376547	CMK	blood:	n/a
19	chrX:80377379-80377429	AoSMC	blood vessel:	n/a
20	chrX:80457315-80457365	MCF10A-Er-Src	breast:	n/a
21	chrX:80457567-80457617	HL-60	blood:	n/a
22	chrX:80457709-80457759	GM12891	blood:	n/a
23	chrX:80457567-80457617	HCM	heart:	n/a
24	chrX:80457681-80457731	HL-60	blood:	n/a
25	chrX:80457681-80457731	HepG2	liver:	n/a
26	chrX:80457518-80457568	AG04449	skin:	fetal
27	chrX:80457709-80457759	SK-N-SH	brain:	n/a
28	chrX:80457567-80457617	HRE	kidney:	n/a
29	chrX:80376497-80376547	K562	blood:	n/a
30	chrX:80457960-80458010	BE2_C	brain:	n/a
31	chrX:80457607-80457657	NHDF-neo	bronchial:	n/a
32	chrX:80377379-80377429	HCT-116	colon:	n/a
33	chrX:80457518-80457568	HL-60	blood:	n/a
34	chrX:80457315-80457365	HCT-116	colon:	n/a
35	chrX:80457960-80458010	SK-N-MC	brain:	n/a
36	chrX:80457960-80458010	AG04449	skin:	fetal
37	chrX:80457015-80457065	HRCEpiC	kidney:	n/a
38	chrX:80457531-80457581	HEK293	kidney:	embryo
39	chrX:80457315-80457365	HRCEpiC	kidney:	n/a
40	chrX:80457607-80457657	HEK293	kidney:	embryo
41	chrX:80457567-80457617	SAEC	small airway:	n/a
42	chrX:80457567-80457617	IMR90	lung:	fetal
43	chrX:80457681-80457731	GM19239	blood:	n/a
44	chrX:80457518-80457568	NH-A	brain:	n/a
45	chrX:80457681-80457731	Caco-2	colon:	n/a
46	chrX:80458049-80458099	HRPEpiC	eye:	n/a
47	chrX:80377379-80377429	Caco-2	colon:	n/a
48	chrX:80377408-80377458	T-47D	breast:	n/a
49	chrX:80457556-80457606	Jurkat	blood:	n/a
50	chrX:80377408-80377458	AG04450	lung:	fetal

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:80063567..80065637-chrX:80375984..80378858,4	K562	blood:
2	chr10:97123108..97123847-chrX:80734146..80734740,2	MCF-7	breast:
3	chrX:80451825..80453880-chrX:80456204..80458319,2	K562	blood:
4	chrX:80463639..80464292-chrX:80541572..80542095,3	MCF-7	breast:
5	chrX:80429828..80430525-chrX:80632522..80633355,3	MCF-7	breast:
6	chr6:26031679..26032193-chrX:80803413..80803913,2	HCT-116	colon:
7	chrX:80415450..80419276-chrX:80420796..80424104,3	K562	blood:
8	chrX:80514794..80516843-chrX:80519998..80521762,2	MCF-7	breast:
9	chrX:80451091..80451885-chrX:80632732..80633503,2	MCF-7	breast:
10	chrX:80460102..80462227-chrX:80465188..80467395,2	K562	blood:
11	chrX:80365897..80368634-chrX:80421665..80423478,2	K562	blood:
12	chrX:80463397..80464935-chrX:80541027..80542503,5	MCF-7	breast:
13	chrX:80460447..80463221-chrX:80540924..80543003,2	MCF-7	breast:
14	chrX:80463639..80464292-chrX:80541572..80542095,3	MCF-7	breast:
15	chrX:80828745..80830467-chrX:80833784..80835592,2	K562	blood:
16	chrX:80828745..80830467-chrX:80833784..80835592,2	K562	blood:
17	chrX:80618854..80620845-chrX:80623113..80625681,2	K562	blood:
18	chrX:80460447..80463221-chrX:80540924..80543003,2	MCF-7	breast:
19	chrX:80514794..80516843-chrX:80519998..80521762,2	MCF-7	breast:
20	chrX:80067488..80068198-chrX:80376211..80376936,2	MCF-7	breast:
21	chrX:80415450..80419276-chrX:80420796..80424104,3	K562	blood:
22	chrX:80375652..80377990-chrX:80380557..80382581,2	K562	blood:
23	chrX:80451192..80454007-chrX:80455781..80458708,2	MCF-7	breast:
24	chrX:80460102..80462227-chrX:80465188..80467395,2	K562	blood:
25	chrX:80618854..80620845-chrX:80623113..80625681,2	K562	blood:
26	chrX:80370253..80374071-chrX:80375369..80378475,3	K562	blood:
27	chrX:80429934..80430440-chrX:80632613..80633144,2	MCF-7	breast:
28	chrX:80463397..80464935-chrX:80541027..80542503,5	MCF-7	breast:
29	chr17:57920504..57923092-chrX:80421236..80423293,2	MCF-7	breast:
30	chrX:80801227..80802774-chrX:80810301..80812266,2	K562	blood:
31	chrX:80447562..80449703-chrX:80455416..80458184,2	K562	blood:
32	chrX:80550801..80553348-chrX:80553971..80556277,2	MCF-7	breast:
33	chrX:80618587..80623507-chrX:80626286..80630162,4	MCF-7	breast:
34	chrX:80450950..80451646-chrX:80632555..80633131,2	MCF-7	breast:
35	chrX:80451091..80451885-chrX:80632732..80633503,2	MCF-7	breast:
36	chrX:80429828..80430525-chrX:80632522..80633355,3	MCF-7	breast:
37	chrX:80450950..80451646-chrX:80632555..80633131,2	MCF-7	breast:
38	chrX:80368168..80369993-chrX:80375695..80377271,2	K562	blood:
39	chrX:80429934..80430440-chrX:80632613..80633144,2	MCF-7	breast:
40	chrX:80132313..80133096-chrX:80376286..80376996,4	MCF-7	breast:
41	chrX:80801227..80802774-chrX:80810301..80812266,2	K562	blood:
42	chrX:80550801..80553348-chrX:80553971..80556277,2	MCF-7	breast:
43	chrX:80365897..80368634-chrX:80421665..80423478,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3BGRL-2	chrX:80618767-80619669	NONHSAT137735
2	lnc-SH3BGRL-1	chrX:80583971-80585393	NONHSAT137734

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SH3BGRL	hsa-miR-128-3p	chrX:80552722-80552742
2	SH3BGRL	hsa-miR-128-3p	chrX:80552727-80552742

Variant related genes	Relation type
ENSG00000233446	TF binding region
ENSG00000231875	TF binding region
ENSG00000224523	TF binding region
ENSG00000264374	TF binding region
HMGN5	TF binding region
SH3BGRL	TF binding region
ENSG00000233446	CpG island
ENSG00000231875	CpG island
ENSG00000224523	CpG island
ENSG00000264374	CpG island
HMGN5	CpG island
SH3BGRL	CpG island
ENSG00000165288	chromatin interactions
ENSG00000198157	chromatin interactions
ENSG00000231875	chromatin interactions
ENSG00000131171	chromatin interactions

Extended variants
information (count: 3046 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:3046 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556864618	chrX:80367211-80367212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149779706	chrX:80367416-80367417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191019123	chrX:80367594-80367595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73631717	chrX:80367645-80367646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185243965	chrX:80367718-80367719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375333794	chrX:80367783-80367784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189704383	chrX:80367990-80367991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182742639	chrX:80368034-80368035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188113524	chrX:80368226-80368227	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145604422	chrX:80368302-80368303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369527181	chrX:80368359-80368360	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73508636	chrX:80368481-80368482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145411525	chrX:80368499-80368500	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs369359290	chrX:80368511-80368512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs146487904	chrX:80368518-80368519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191759421	chrX:80368588-80368589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2337002	chrX:80368740-80368741	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs183676044	chrX:80368804-80368805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188894586	chrX:80368839-80368840	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1937292	chrX:80368850-80368851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143947740	chrX:80368878-80368879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs73631718	chrX:80368931-80368932	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1937291	chrX:80368950-80368951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs1937290	chrX:80369110-80369111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs199672193	chrX:80369290-80369291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148228755	chrX:80369293-80369294	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs68183777	chrX:80369628-80369629	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs41300259	chrX:80369834-80369835	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs541764526	chrX:80369900-80369901	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs41300251	chrX:80369975-80369976	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184579787	chrX:80369993-80369994	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs41310713	chrX:80370164-80370165	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs186732408	chrX:80370251-80370252	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369429467	chrX:80370286-80370287	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111213569	chrX:80370369-80370370	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs374637006	chrX:80370451-80370452	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142186197	chrX:80370486-80370487	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144502161	chrX:80370502-80370503	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs147858164	chrX:80370532-80370533	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148928737	chrX:80370630-80370631	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143679569	chrX:80370668-80370669	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs59584935	chrX:80370716-80370717	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376593790	chrX:80370738-80370739	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369561571	chrX:80370978-80370979	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs184807507	chrX:80371014-80371015	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374617762	chrX:80371105-80371106	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1937289	chrX:80371446-80371447	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs113583771	chrX:80371658-80371659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs148090107	chrX:80371768-80371769	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs143325725	chrX:80371918-80371919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:41)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1766 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:80366800-80375400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chrX:80367400-80375800	Weak transcription	Brain Substantia Nigra	brain
3	chrX:80368200-80370200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chrX:80369000-80375000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chrX:80369400-80375000	Weak transcription	Hela-S3	cervix
6	chrX:80369400-80375200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chrX:80369800-80370400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
8	chrX:80370200-80370800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chrX:80370200-80371000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
10	chrX:80370400-80371600	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chrX:80370800-80375400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chrX:80371000-80375000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chrX:80371600-80372200	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chrX:80372800-80375600	Weak transcription	Fetal Intestine Small	intestine
15	chrX:80373600-80378000	Active TSS	GM12878-XiMat	blood
16	chrX:80374800-80375000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chrX:80374800-80375200	Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chrX:80374800-80375400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chrX:80374800-80378000	Active TSS	K562	blood
20	chrX:80375000-80375200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chrX:80375000-80375200	Enhancers	Hela-S3	cervix
22	chrX:80375000-80375400	Enhancers	Liver	Liver
23	chrX:80375000-80375600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chrX:80375000-80377800	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chrX:80375200-80375400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chrX:80375200-80375400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chrX:80375200-80375400	Active TSS	Fetal Brain Female	brain
28	chrX:80375200-80375600	Enhancers	Primary T cells from cord blood	blood
29	chrX:80375200-80375600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chrX:80375200-80375600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chrX:80375200-80376000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chrX:80375200-80377600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chrX:80375200-80377600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chrX:80375200-80377600	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chrX:80375200-80377800	Active TSS	HUES48 Cell Line	embryonic stem cell
36	chrX:80375200-80377800	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chrX:80375200-80378000	Active TSS	Brain Germinal Matrix	brain
38	chrX:80375200-80378000	Active TSS	Hela-S3	cervix
39	chrX:80375200-80378200	Active TSS	H1 Cell Line	embryonic stem cell
40	chrX:80375400-80375600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
41	chrX:80375400-80375600	Enhancers	Primary monocytes fromperipheralblood	blood
42	chrX:80375400-80375600	Active TSS	Primary B cells from cord blood	blood
43	chrX:80375400-80375600	Enhancers	Primary B cells from peripheral blood	blood
44	chrX:80375400-80375600	Enhancers	Primary T cells fromperipheralblood	blood
45	chrX:80375400-80375600	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chrX:80375400-80375600	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chrX:80375400-80375600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chrX:80375400-80375600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chrX:80375400-80375600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chrX:80375400-80375600	Enhancers	Adipose Nuclei	Adipose

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