Variant report

Variant	nsv580974
Chromosome Location	chr2:11867841-11898931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2246)
CpG islands
(count:1283)
Chromatin interactive
region (count:46)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2246 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:11886470-11886670	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:11884041-11884638	K562	blood:	n/a	n/a
3	ARID3A	chr2:11896311-11896484	K562	blood:	n/a	n/a
4	ARID3A	chr2:11884128-11884621	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:11885337-11885557	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:11893708-11894050	K562	blood:	n/a	n/a
7	ARID3A	chr2:11885849-11885951	K562	blood:	n/a	n/a
8	ARID3A	chr2:11875899-11876054	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:11886593-11886619	K562	blood:	n/a	n/a
10	ARID3A	chr2:11878746-11878837	K562	blood:	n/a	n/a
11	ATF1	chr2:11884089-11884582	K562	blood:	n/a	n/a
12	ATF1	chr2:11893642-11894295	K562	blood:	n/a	n/a
13	ATF2	chr2:11893373-11894172	GM12878	blood:	n/a	n/a
14	ATF2	chr2:11883900-11884645	GM12878	blood:	n/a	n/a
15	ATF2	chr2:11893357-11894827	GM12878	blood:	n/a	n/a
16	ATF2	chr2:11883996-11884600	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:11884038-11884673	GM12878	blood:	n/a	n/a
18	ATF2	chr2:11889831-11890411	GM12878	blood:	n/a	n/a
19	ATF2	chr2:11883995-11884589	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr2:11889745-11891404	GM12878	blood:	n/a	n/a
21	ATF2	chr2:11890416-11891493	GM12878	blood:	n/a	n/a
22	ATF3	chr2:11884071-11884600	K562	blood:	n/a	n/a
23	ATF3	chr2:11884155-11884520	K562	blood:	n/a	n/a
24	ATF3	chr2:11883851-11884683	A549	lung:	n/a	n/a
25	ATF3	chr2:11886568-11886953	K562	blood:	n/a	n/a
26	ATF3	chr2:11883896-11884621	A549	lung:	n/a	n/a
27	BACH1	chr2:11884114-11884607	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr2:11884073-11884566	K562	blood:	n/a	n/a
29	BACH1	chr2:11886479-11887426	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr2:11893594-11894120	GM12878	blood:	n/a	n/a
31	BATF	chr2:11884063-11884582	GM12878	blood:	n/a	chr2:11884301-11884312
32	BATF	chr2:11893468-11894141	GM12878	blood:	n/a	n/a
33	BATF	chr2:11889954-11890298	GM12878	blood:	n/a	n/a
34	BATF	chr2:11884163-11884501	GM12878	blood:	n/a	chr2:11884301-11884312
35	BATF	chr2:11894257-11894698	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:11889931-11890311	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:11891045-11891457	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:11893524-11893942	GM12878	blood:	n/a	chr2:11893912-11893921
39	BCL11A	chr2:11889970-11890340	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:11894789-11895070	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:11884071-11884592	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:11893449-11894214	GM12878	blood:	n/a	chr2:11893912-11893921
43	BCL11A	chr2:11894285-11894584	GM12878	blood:	n/a	n/a
44	BCL3	chr2:11883883-11884682	A549	lung:	n/a	n/a
45	BCL3	chr2:11883942-11884601	GM12878	blood:	n/a	n/a
46	BCL3	chr2:11884163-11884463	GM12878	blood:	n/a	n/a
47	BCL3	chr2:11883899-11885397	A549	lung:	n/a	n/a
48	BCL3	chr2:11893491-11893968	GM12878	blood:	n/a	chr2:11893912-11893921
49	BCL3	chr2:11886333-11886874	A549	lung:	n/a	chr2:11886745-11886758 chr2:11886834-11886847
50	BCL3	chr2:11882447-11882803	GM12878	blood:	n/a	chr2:11882642-11882651

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:11885321-11885371	NT2-D1	testis:	n/a
2	chr2:11888753-11888803	HRE	kidney:	n/a
3	chr2:11885321-11885371	NT2-D1	testis:	n/a
4	chr2:11888753-11888803	HRE	kidney:	n/a
5	chr2:11887322-11887372	IMR90	lung:	fetal
6	chr2:11887322-11887372	SK-N-SH_RA	brain:	n/a
7	chr2:11888753-11888803	Hela-S3	cervix:	n/a
8	chr2:11881338-11881388	SKMC	muscle:	n/a
9	chr2:11885266-11885316	NHDF-neo	bronchial:	n/a
10	chr2:11894464-11894514	HMEC	breast:	n/a
11	chr2:11881462-11881512	SAEC	small airway:	n/a
12	chr2:11881338-11881388	GM12878	blood:	n/a
13	chr2:11878864-11878914	K562	blood:	n/a
14	chr2:11884333-11884383	BE2_C	brain:	n/a
15	chr2:11887322-11887372	BE2_C	brain:	n/a
16	chr2:11886589-11886639	MCF-7	breast:	n/a
17	chr2:11885560-11885610	Hela-S3	cervix:	n/a
18	chr2:11881462-11881512	HEK293	kidney:	embryo
19	chr2:11885321-11885371	U87	brain:	n/a
20	chr2:11886400-11886450	AG04449	skin:	fetal
21	chr2:11884333-11884383	MCF10A-Er-Src	breast:	n/a
22	chr2:11878864-11878914	ProgFib	skin:	n/a
23	chr2:11887120-11887170	ECC-1	luminal epithelium:	n/a
24	chr2:11867801-11867851	PFSK-1	brain:	n/a
25	chr2:11883947-11883997	HRCEpiC	kidney:	n/a
26	chr2:11885560-11885610	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:11881462-11881512	HCT-116	colon:	n/a
28	chr2:11883947-11883997	BJ	skin:	n/a
29	chr2:11881225-11881275	AG09309	skin:	n/a
30	chr2:11890700-11890750	PANC-1	pancreas:	n/a
31	chr2:11887322-11887372	K562	blood:	n/a
32	chr2:11885560-11885610	AG10803	skin:	n/a
33	chr2:11886253-11886303	GM19239	blood:	n/a
34	chr2:11894464-11894514	BJ	skin:	n/a
35	chr2:11894464-11894514	SK-N-MC	brain:	n/a
36	chr2:11886589-11886639	NH-A	brain:	n/a
37	chr2:11885266-11885316	Caco-2	colon:	n/a
38	chr2:11887322-11887372	PANC-1	pancreas:	n/a
39	chr2:11894464-11894514	Hepatocyte	liver:	n/a
40	chr2:11885321-11885371	CMK	blood:	n/a
41	chr2:11886637-11886687	SK-N-SH	brain:	n/a
42	chr2:11886253-11886303	H1-hESC	embryonic stem cell:	embryo
43	chr2:11884333-11884383	HCT-116	colon:	n/a
44	chr2:11884333-11884383	LNCaP	prostate:	n/a
45	chr2:11886613-11886663	HCPEpiC	choroid plexus:	n/a
46	chr2:11886400-11886450	RPTEC	kidney:	n/a
47	chr2:11881462-11881512	HNPCEpiC	eye:	n/a
48	chr2:11886253-11886303	GM12878	blood:	n/a
49	chr2:11886613-11886663	PFSK-1	brain:	n/a
50	chr2:11885266-11885316	AoSMC	blood vessel:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:11886726..11888240-chr2:11889703..11892013,2	MCF-7	breast:
2	chr2:11850515..11852161-chr2:11877592..11880491,2	MCF-7	breast:
3	chr2:11885383..11891655-chr2:11894666..11900002,13	K562	blood:
4	chr2:11893238..11895926-chr2:11901659..11904630,2	MCF-7	breast:
5	chr2:11887777..11889810-chr2:11903193..11905347,2	K562	blood:
6	chr2:11872488..11875860-chr2:11884452..11886628,3	K562	blood:
7	chr2:10259345..10261058-chr2:11886635..11888299,2	K562	blood:
8	chr2:11892034..11894418-chr2:11895630..11897983,2	K562	blood:
9	chr2:11886095..11889149-chr2:11892372..11895802,5	MCF-7	breast:
10	chr2:11869912..11872464-chr2:11874565..11877057,2	K562	blood:
11	chr2:11882616..11883484-chr2:11891634..11892366,2	K562	blood:
12	chr2:11872902..11875689-chr2:11878776..11880592,2	K562	blood:
13	chr2:11883702..11885372-chr2:11901343..11903845,2	K562	blood:
14	chr2:11882438..11884776-chr2:11910789..11914613,4	K562	blood:
15	chr2:11878418..11879254-chr2:11919121..11919879,2	MCF-7	breast:
16	chr2:11882411..11885202-chr2:11902345..11904670,2	K562	blood:
17	chr2:11882616..11883484-chr2:11891634..11892366,2	K562	blood:
18	chr2:11882508..11884186-chr2:11887506..11889026,2	MCF-7	breast:
19	chr2:11894229..11895862-chr2:11899704..11901384,2	K562	blood:
20	chr2:11604833..11608003-chr2:11882353..11886330,4	K562	blood:
21	chr2:11604255..11606398-chr2:11886112..11888104,2	K562	blood:
22	chr2:11879500..11881190-chr2:11886379..11888798,2	MCF-7	breast:
23	chr2:11885343..11888558-chr2:11916972..11921085,4	K562	blood:
24	chr2:11875528..11877148-chr2:11877418..11878938,2	MCF-7	breast:
25	chr2:11875528..11877148-chr2:11877418..11878938,2	MCF-7	breast:
26	chr2:11798417..11800277-chr2:11891878..11893871,2	K562	blood:
27	chr2:11872902..11874772-chr2:11878776..11881694,2	K562	blood:
28	chr2:11869912..11872464-chr2:11874565..11877057,2	K562	blood:
29	chr2:11872902..11875689-chr2:11878776..11880592,2	K562	blood:
30	chr2:11892034..11894418-chr2:11895630..11897983,2	K562	blood:
31	chr2:11870195..11872088-chr2:11885962..11887641,2	MCF-7	breast:
32	chr2:11864143..11867018-chr2:11871062..11872663,2	K562	blood:
33	chr2:11872902..11874772-chr2:11878776..11881694,2	K562	blood:
34	chr2:11886833..11889158-chr2:11909295..11910808,2	K562	blood:
35	chr2:11878332..11879441-chr2:11918884..11919993,17	MCF-7	breast:
36	chr2:11881178..11885762-chr2:11886043..11889477,7	MCF-7	breast:
37	chr2:11864844..11866571-chr2:11873207..11875042,2	K562	blood:
38	chr2:11881178..11885762-chr2:11886043..11889477,7	MCF-7	breast:
39	chr2:11867421..11869594-chr2:11885775..11887572,2	MCF-7	breast:
40	chr10:32078085..32079585-chr2:11880425..11883011,2	MCF-7	breast:
41	chr2:11890007..11892295-chr2:11917973..11920590,2	K562	blood:
42	chr2:11878641..11879395-chr2:11919018..11919604,3	K562	blood:
43	chr2:11678361..11681033-chr2:11884649..11887386,2	MCF-7	breast:
44	chr2:11876175..11878551-chr2:11884561..11886899,2	K562	blood:
45	chr2:11827642..11829503-chr2:11889193..11891335,2	MCF-7	breast:
46	chr2:11882508..11884186-chr2:11887506..11889026,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GREB1-9	chr2:11881475-11881554	NONHSAT069191
2	lnc-NTSR2-2	chr2:11885293-11885427	ENSG00000230790.2
3	lnc-GREB1-9	chr2:11886087-11886256	NONHSAT069191
4	lnc-GREB1-9	chr2:11881475-11881554	NONHSAT069192
5	lnc-NTSR2-2	chr2:11881123-11881428	ENSG00000230790.2
6	lnc-NTSR2-2	chr2:11882163-11882282	ENSG00000230790.2
7	lnc-GREB1-9	chr2:11886033-11886256	NONHSAT069192

No data

Variant related genes	Relation type
ENSG00000203643	TF binding region
ENSG00000230790	TF binding region
LPIN1	TF binding region
ENSG00000203643	CpG island
ENSG00000230790	CpG island
LPIN1	CpG island
ENSG00000264010	chromatin interactions
ENSG00000134324	chromatin interactions
ENSG00000169016	chromatin interactions
ENSG00000203643	chromatin interactions
ENSG00000196208	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000230790	chromatin interactions

Extended variants
information (count: 1226 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1226 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13384037	chr2:11867841-11867842	Inactive region	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575326705	chr2:11867842-11867843	Inactive region	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs187540519	chr2:11867856-11867857	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs116645669	chr2:11867936-11867937	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs146446941	chr2:11867955-11867956	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs547635870	chr2:11868019-11868020	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs192401753	chr2:11868026-11868027	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs138986358	chr2:11868027-11868028	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551404336	chr2:11868033-11868034	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs568899838	chr2:11868120-11868121	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs140510246	chr2:11868153-11868154	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs569706655	chr2:11868202-11868203	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs530624132	chr2:11868224-11868225	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548830721	chr2:11868301-11868302	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567830222	chr2:11868357-11868358	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs150420339	chr2:11868363-11868364	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs185766644	chr2:11868365-11868366	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571618406	chr2:11868378-11868379	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs138205856	chr2:11868412-11868413	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575579921	chr2:11868440-11868441	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543091981	chr2:11868489-11868490	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs554781426	chr2:11868515-11868516	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573751639	chr2:11868597-11868598	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540872279	chr2:11868614-11868615	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559644272	chr2:11868616-11868617	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370081226	chr2:11868631-11868632	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373830001	chr2:11868668-11868669	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533253722	chr2:11868703-11868704	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545366342	chr2:11868750-11868751	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs62113266	chr2:11868784-11868785	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs190489997	chr2:11868790-11868791	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549036809	chr2:11868826-11868827	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs61415061	chr2:11868834-11868835	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs397967670	chr2:11868842-11868843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs72773972	chr2:11868870-11868871	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192656026	chr2:11868922-11868923	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553797972	chr2:11868964-11868965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs149622404	chr2:11868967-11868968	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571556072	chr2:11869042-11869043	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570401586	chr2:11869051-11869052	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184501865	chr2:11869054-11869055	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557267056	chr2:11869079-11869080	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78014870	chr2:11869177-11869178	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs62113267	chr2:11869208-11869209	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs72773973	chr2:11869217-11869218	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs543959224	chr2:11869218-11869219	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188545348	chr2:11869240-11869241	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573266278	chr2:11869297-11869298	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs146122821	chr2:11869315-11869316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553198075	chr2:11869319-11869320	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	20607354	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1680 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11869600-11869800	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr2:11869600-11870400	Enhancers	Dnd41	blood
3	chr2:11869800-11870400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr2:11870400-11870600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr2:11874000-11874400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:11874200-11874800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:11874200-11874800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr2:11874400-11874800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:11874400-11875000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:11874400-11876400	Enhancers	Fetal Intestine Large	intestine
11	chr2:11874800-11875200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr2:11874800-11878800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr2:11875000-11878800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr2:11875200-11883000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr2:11875600-11876000	Enhancers	Fetal Intestine Small	intestine
16	chr2:11875600-11876400	Enhancers	HepG2	liver
17	chr2:11875800-11876000	Enhancers	Colonic Mucosa	Colon
18	chr2:11875800-11876000	Enhancers	Hela-S3	cervix
19	chr2:11875800-11877000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:11876000-11876200	Enhancers	Fetal Thymus	thymus
21	chr2:11876000-11876800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:11876000-11878600	Weak transcription	Colonic Mucosa	Colon
23	chr2:11876000-11878600	Weak transcription	Hela-S3	cervix
24	chr2:11876200-11878600	Weak transcription	Liver	Liver
25	chr2:11876400-11877000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr2:11876400-11877200	Enhancers	Psoas Muscle	Psoas
27	chr2:11876600-11877000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr2:11876800-11877000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:11876800-11877400	Enhancers	Dnd41	blood
30	chr2:11876800-11878600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:11877000-11878400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:11877000-11882800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:11877000-11883400	Weak transcription	Right Atrium	heart
34	chr2:11877200-11878600	Weak transcription	Psoas Muscle	Psoas
35	chr2:11878400-11878600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:11878400-11879200	Enhancers	Right Ventricle	heart
37	chr2:11878400-11879400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr2:11878400-11879600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:11878400-11880000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:11878600-11878800	Enhancers	Colonic Mucosa	Colon
41	chr2:11878600-11878800	Enhancers	Fetal Intestine Small	intestine
42	chr2:11878600-11878800	Enhancers	Fetal Thymus	thymus
43	chr2:11878600-11878800	Enhancers	HepG2	liver
44	chr2:11878600-11878800	Enhancers	K562	blood
45	chr2:11878600-11879000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr2:11878600-11879000	Enhancers	Primary B cells from peripheral blood	blood
47	chr2:11878600-11879000	Enhancers	Primary T cells fromperipheralblood	blood
48	chr2:11878600-11879000	Enhancers	Brain Cingulate Gyrus	brain
49	chr2:11878600-11879000	Enhancers	Rectal Smooth Muscle	rectum
50	chr2:11878600-11879000	Bivalent Enhancer	GM12878-XiMat	blood

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