Variant report

Variant	nsv818809
Chromosome Location	chr11:34239730-34354076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2015)
CpG islands
(count:856)
Chromatin interactive
region (count:114)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34240422-34240643	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:34339955-34340500	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:34331458-34331706	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:34272488-34272500	K562	blood:	n/a	n/a
5	ARID3A	chr11:34263663-34263838	K562	blood:	n/a	n/a
6	ARID3A	chr11:34330729-34331219	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:34258144-34258360	K562	blood:	n/a	n/a
8	ARID3A	chr11:34338651-34338851	HepG2	liver:	n/a	n/a
9	ATF1	chr11:34271202-34271360	K562	blood:	n/a	n/a
10	ATF1	chr11:34258159-34258470	K562	blood:	n/a	n/a
11	ATF1	chr11:34263622-34264047	K562	blood:	n/a	n/a
12	ATF1	chr11:34255636-34255924	K562	blood:	n/a	n/a
13	ATF1	chr11:34264548-34264774	K562	blood:	n/a	n/a
14	ATF2	chr11:34263526-34263963	GM12878	blood:	n/a	n/a
15	ATF2	chr11:34253173-34253663	GM12878	blood:	n/a	n/a
16	ATF2	chr11:34255499-34256159	GM12878	blood:	n/a	n/a
17	ATF2	chr11:34256665-34257227	GM12878	blood:	n/a	n/a
18	ATF2	chr11:34265540-34266147	GM12878	blood:	n/a	n/a
19	ATF2	chr11:34255380-34256269	GM12878	blood:	n/a	n/a
20	ATF2	chr11:34256641-34257339	GM12878	blood:	n/a	n/a
21	ATF2	chr11:34265488-34266211	GM12878	blood:	n/a	n/a
22	ATF2	chr11:34261244-34261828	GM12878	blood:	n/a	n/a
23	ATF2	chr11:34324042-34324553	GM12878	blood:	n/a	n/a
24	ATF2	chr11:34255540-34255940	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr11:34323938-34324575	GM12878	blood:	n/a	n/a
26	ATF3	chr11:34264947-34265689	A549	lung:	n/a	n/a
27	ATF3	chr11:34296192-34296750	A549	lung:	n/a	chr11:34296469-34296480 chr11:34296470-34296481 chr11:34296467-34296480 chr11:34296459-34296479 chr11:34296471-34296481 chr11:34296467-34296482 chr11:34296470-34296478 chr11:34296468-34296478 chr11:34296467-34296478 chr11:34296469-34296482 chr11:34296471-34296478 chr11:34296468-34296481
28	BACH1	chr11:34265215-34265539	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr11:34337547-34337584	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr11:34255562-34255974	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr11:34255571-34256220	GM12878	blood:	n/a	n/a
32	BATF	chr11:34270025-34270281	GM12878	blood:	n/a	n/a
33	BATF	chr11:34323976-34324512	GM12878	blood:	n/a	chr11:34324172-34324182
34	BATF	chr11:34265565-34266061	GM12878	blood:	n/a	n/a
35	BATF	chr11:34253222-34253532	GM12878	blood:	n/a	n/a
36	BATF	chr11:34256617-34257256	GM12878	blood:	n/a	n/a
37	BATF	chr11:34261472-34261820	GM12878	blood:	n/a	n/a
38	BATF	chr11:34265298-34266102	GM12878	blood:	n/a	n/a
39	BATF	chr11:34324025-34324515	GM12878	blood:	n/a	chr11:34324172-34324182
40	BATF	chr11:34256722-34257234	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:34265561-34266037	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:34253175-34253472	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:34324010-34324466	GM12878	blood:	n/a	chr11:34324174-34324183 chr11:34324175-34324184
44	BCL11A	chr11:34256644-34257202	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:34256783-34257188	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:34261392-34261842	GM12878	blood:	n/a	chr11:34261556-34261565
47	BCL11A	chr11:34265602-34266021	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:34324042-34324477	GM12878	blood:	n/a	chr11:34324174-34324183 chr11:34324175-34324184
49	BCL11A	chr11:34269972-34270387	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:34255701-34256085	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34288225-34288275	SAEC	small airway:	n/a
2	chr11:34288225-34288275	AG04450	lung:	fetal
3	chr11:34288225-34288275	SAEC	small airway:	n/a
4	chr11:34288225-34288275	AG04450	lung:	fetal
5	chr11:34296462-34296512	GM06990	blood:	n/a
6	chr11:34285529-34285579	GM06990	blood:	n/a
7	chr11:34273111-34273161	GM12878	blood:	n/a
8	chr11:34340108-34340158	HIPEpiC	eye:	n/a
9	chr11:34296462-34296512	AG09309	skin:	n/a
10	chr11:34284610-34284660	AG04450	lung:	fetal
11	chr11:34284610-34284660	HL-60	blood:	n/a
12	chr11:34273111-34273161	SK-N-SH_RA	brain:	n/a
13	chr11:34255733-34255783	PFSK-1	brain:	n/a
14	chr11:34265361-34265411	BJ	skin:	n/a
15	chr11:34265361-34265411	SKMC	muscle:	n/a
16	chr11:34244798-34244848	HRPEpiC	eye:	n/a
17	chr11:34285529-34285579	AG09309	skin:	n/a
18	chr11:34296462-34296512	SKMC	muscle:	n/a
19	chr11:34296462-34296512	IMR90	lung:	fetal
20	chr11:34288225-34288275	T-47D	breast:	n/a
21	chr11:34256703-34256753	HCF	heart:	n/a
22	chr11:34244798-34244848	GM06990	blood:	n/a
23	chr11:34323678-34323728	AG09319	gingival:	n/a
24	chr11:34323678-34323728	HCF	heart:	n/a
25	chr11:34273111-34273161	ECC-1	luminal epithelium:	n/a
26	chr11:34331908-34331958	HEEpiC	esophagus:	n/a
27	chr11:34265361-34265411	NHDF-neo	bronchial:	n/a
28	chr11:34322226-34322276	HRPEpiC	eye:	n/a
29	chr11:34273111-34273161	CMK	blood:	n/a
30	chr11:34350440-34350490	BE2_C	brain:	n/a
31	chr11:34340108-34340158	AG09309	skin:	n/a
32	chr11:34255733-34255783	NHBE	bronchial:	n/a
33	chr11:34256703-34256753	GM12878	blood:	n/a
34	chr11:34323678-34323728	HEEpiC	esophagus:	n/a
35	chr11:34265361-34265411	ovcar-3	ovarian:	n/a
36	chr11:34322226-34322276	AG09309	skin:	n/a
37	chr11:34350440-34350490	HRE	kidney:	n/a
38	chr11:34288225-34288275	GM06990	blood:	n/a
39	chr11:34285529-34285579	Hepatocyte	liver:	n/a
40	chr11:34331908-34331958	AoSMC	blood vessel:	n/a
41	chr11:34256703-34256753	RPTEC	kidney:	n/a
42	chr11:34244798-34244848	H1-hESC	embryonic stem cell:	embryo
43	chr11:34288225-34288275	IMR90	lung:	fetal
44	chr11:34340108-34340158	SK-N-SH_RA	brain:	n/a
45	chr11:34284610-34284660	HEEpiC	esophagus:	n/a
46	chr11:34265361-34265411	HRE	kidney:	n/a
47	chr11:34244798-34244848	SK-N-SH	brain:	n/a
48	chr11:34288225-34288275	GM12878	blood:	n/a
49	chr11:34285529-34285579	HRE	kidney:	n/a
50	chr11:34284610-34284660	HPAEpiC	pulmonary alveolar:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:34346331..34348538-chr11:34354788..34356481,2	MCF-7	breast:
2	chr11:34278645..34281276-chr11:34285188..34287550,2	K562	blood:
3	chr11:34329413..34331132-chr11:34333216..34335602,2	K562	blood:
4	chr11:34328956..34331154-chr11:34336268..34338352,2	K562	blood:
5	chr11:34278605..34281312-chr11:34339472..34341100,2	K562	blood:
6	chr11:34231932..34233684-chr11:34247435..34249545,2	K562	blood:
7	chr11:34257238..34258836-chr11:34262928..34265413,2	MCF-7	breast:
8	chr11:34308939..34311768-chr11:34379486..34381875,2	MCF-7	breast:
9	chr11:34146428..34148195-chr11:34289895..34292755,2	MCF-7	breast:
10	chr11:34268801..34271707-chr11:34290725..34293055,2	K562	blood:
11	chr11:34260780..34263020-chr11:34279926..34282268,2	MCF-7	breast:
12	chr11:34267721..34270365-chr11:34272865..34274585,2	MCF-7	breast:
13	chr11:34306120..34306999-chr11:34317675..34318487,2	MCF-7	breast:
14	chr11:34285128..34287533-chr11:34298437..34301296,2	MCF-7	breast:
15	chr11:34243758..34246398-chr11:34366962..34369270,2	MCF-7	breast:
16	chr11:34297526..34299830-chr11:34304007..34305753,2	MCF-7	breast:
17	chr11:34284799..34287708-chr11:34289917..34291890,2	K562	blood:
18	chr11:34309410..34312078-chr11:34318122..34319816,2	K562	blood:
19	chr11:34342106..34344369-chr11:34352747..34354682,2	MCF-7	breast:
20	chr11:34330140..34331933-chr11:34345300..34347720,2	K562	blood:
21	chr11:34244635..34246968-chr11:34254314..34256180,3	K562	blood:
22	chr11:34331497..34333782-chr11:34370435..34371982,2	MCF-7	breast:
23	chr11:34345030..34348316-chr11:34348388..34351447,3	K562	blood:
24	chr11:34309410..34312078-chr11:34318122..34319816,2	K562	blood:
25	chr11:34340373..34342036-chr11:34343616..34346378,2	MCF-7	breast:
26	chr11:34295969..34298454-chr11:34328816..34331408,3	MCF-7	breast:
27	chr11:34261414..34263986-chr11:34271757..34273793,2	K562	blood:
28	chr11:34261414..34263986-chr11:34271757..34273793,2	K562	blood:
29	chr11:34295048..34297358-chr11:34352691..34354542,2	MCF-7	breast:
30	chr11:34242165..34244908-chr11:34379144..34380922,2	MCF-7	breast:
31	chr11:34297526..34299830-chr11:34304007..34305753,2	MCF-7	breast:
32	chr11:34283686..34286562-chr11:34377473..34379594,2	MCF-7	breast:
33	chr11:34306091..34307062-chr11:34317641..34318576,2	MCF-7	breast:
34	chr11:34239663..34242174-chr11:34378440..34380347,2	MCF-7	breast:
35	chr11:34321619..34323439-chr11:34377216..34379630,2	MCF-7	breast:
36	chr11:34353541..34355614-chr11:34357152..34360138,2	MCF-7	breast:
37	chr11:34306091..34307062-chr11:34317641..34318576,2	MCF-7	breast:
38	chr11:34229441..34231710-chr11:34255472..34258756,3	MCF-7	breast:
39	chr11:34303207..34305928-chr11:34378915..34380855,2	MCF-7	breast:
40	chr11:34306120..34306643-chr11:34317612..34318175,2	MCF-7	breast:
41	chr11:34345532..34347558-chr11:34378083..34380807,2	MCF-7	breast:
42	chr11:34323353..34325328-chr11:34327561..34330383,2	MCF-7	breast:
43	chr11:34284799..34287708-chr11:34289917..34291890,2	K562	blood:
44	chr11:34177633..34180351-chr11:34316571..34318633,2	MCF-7	breast:
45	chr11:34310476..34312267-chr11:34326192..34328969,2	MCF-7	breast:
46	chr11:34329413..34331132-chr11:34333216..34335602,2	K562	blood:
47	chr11:34340373..34342036-chr11:34343616..34346378,2	MCF-7	breast:
48	chr11:34317934..34320439-chr11:34320796..34323680,2	MCF-7	breast:
49	chr11:34278605..34281312-chr11:34339472..34341100,2	K562	blood:
50	chr11:34336235..34339899-chr11:34377222..34380179,3	MCF-7	breast:

No data

Variant related genes	Relation type
ABTB2	TF binding region
ABTB2	CpG island
ENSG00000166016	chromatin interactions
ENSG00000135372	chromatin interactions
ENSG00000254708	chromatin interactions

Extended variants
information (count: 4563 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:4563 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11032561	chr11:34239730-34239731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2746625	chr11:34239806-34239807	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565653652	chr11:34239825-34239826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs289978	chr11:34239877-34239878	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554147246	chr11:34239902-34239903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs574190932	chr11:34239903-34239904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12418582	chr11:34239946-34239947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs557513899	chr11:34239964-34239965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs73491818	chr11:34240014-34240015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2957490	chr11:34240084-34240085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs560051039	chr11:34240086-34240087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573585147	chr11:34240126-34240127	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs185258033	chr11:34240135-34240136	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190124952	chr11:34240141-34240142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112794378	chr11:34240144-34240145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34027222	chr11:34240171-34240172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2092638	chr11:34240172-34240173	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs564627963	chr11:34240180-34240181	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs532174413	chr11:34240187-34240188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551963788	chr11:34240197-34240198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565592599	chr11:34240204-34240205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181188312	chr11:34240226-34240227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs78977608	chr11:34240244-34240245	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567751715	chr11:34240268-34240269	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs367966930	chr11:34240269-34240270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575884995	chr11:34240270-34240271	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145321302	chr11:34240293-34240294	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2092637	chr11:34240357-34240358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs185597559	chr11:34240381-34240382	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs35803950	chr11:34240419-34240420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533170255	chr11:34240437-34240438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113243960	chr11:34240451-34240452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs188743726	chr11:34240466-34240467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs141500137	chr11:34240496-34240497	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573572682	chr11:34240497-34240498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542576823	chr11:34240514-34240515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs562043682	chr11:34240537-34240538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377185252	chr11:34240580-34240581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs140343097	chr11:34240597-34240598	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148092409	chr11:34240598-34240599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs117770300	chr11:34240599-34240600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143855072	chr11:34240600-34240601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs35778027	chr11:34240601-34240602	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs386373555	chr11:34240602-34240603	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369595895	chr11:34240606-34240607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs372016609	chr11:34240607-34240608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376663614	chr11:34240608-34240609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564382566	chr11:34240620-34240621	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs180698021	chr11:34240668-34240669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs911498	chr11:34240676-34240677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:3013 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34219000-34240800	Weak transcription	Left Ventricle	heart
2	chr11:34226600-34244600	Weak transcription	Small Intestine	intestine
3	chr11:34227000-34244400	Weak transcription	Pancreas	Pancrea
4	chr11:34229200-34243000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr11:34230600-34244400	Weak transcription	Right Ventricle	heart
6	chr11:34230800-34241000	Weak transcription	Placenta	Placenta
7	chr11:34232400-34241800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr11:34234800-34241600	Weak transcription	Fetal Muscle Leg	muscle
9	chr11:34235600-34245600	Weak transcription	Spleen	Spleen
10	chr11:34236800-34241200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:34236800-34241800	Weak transcription	Lung	lung
12	chr11:34236800-34244200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:34236800-34244400	Weak transcription	Brain Hippocampus Middle	brain
14	chr11:34237000-34241200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr11:34237000-34241200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr11:34237000-34241200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr11:34237000-34244200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr11:34237000-34244200	Weak transcription	Osteobl	bone
19	chr11:34237000-34244400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:34237000-34244400	Weak transcription	Right Atrium	heart
21	chr11:34237000-34244400	Weak transcription	HSMMtube	muscle
22	chr11:34237200-34240000	Weak transcription	HepG2	liver
23	chr11:34237200-34241200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:34237200-34243800	Weak transcription	Liver	Liver
25	chr11:34237200-34255600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:34238800-34239800	Weak transcription	A549	lung
27	chr11:34239200-34240800	Weak transcription	Psoas Muscle	Psoas
28	chr11:34239400-34242000	Enhancers	Fetal Lung	lung
29	chr11:34239800-34242200	Enhancers	A549	lung
30	chr11:34240000-34242000	Enhancers	HepG2	liver
31	chr11:34240800-34241000	Enhancers	Left Ventricle	heart
32	chr11:34240800-34241000	Enhancers	Psoas Muscle	Psoas
33	chr11:34241000-34241200	Enhancers	Placenta	Placenta
34	chr11:34241000-34241400	Weak transcription	Left Ventricle	heart
35	chr11:34241000-34241400	Weak transcription	Psoas Muscle	Psoas
36	chr11:34241000-34242000	Enhancers	Fetal Heart	heart
37	chr11:34241200-34241400	Bivalent Enhancer	Fetal Kidney	kidney
38	chr11:34241200-34241600	Weak transcription	Placenta	Placenta
39	chr11:34241200-34242000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:34241200-34242000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:34241200-34242000	Enhancers	Colon Smooth Muscle	Colon
42	chr11:34241200-34242000	Enhancers	Fetal Stomach	stomach
43	chr11:34241200-34242200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:34241200-34242200	Enhancers	Adipose Nuclei	Adipose
45	chr11:34241200-34242200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr11:34241200-34243200	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr11:34241400-34242000	Enhancers	Psoas Muscle	Psoas
48	chr11:34241400-34242200	Enhancers	Left Ventricle	heart
49	chr11:34241600-34242000	Enhancers	Fetal Muscle Leg	muscle
50	chr11:34241600-34242200	Enhancers	Placenta	Placenta

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