Variant report

Variant	nsv873409
Chromosome Location	chr1:246122871-246429058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3978)
CpG islands
(count:2626)
Chromatin interactive
region (count:302)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3978 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246315871-246317843	K562	blood:	n/a	n/a
2	ARID3A	chr1:246149980-246150984	K562	blood:	n/a	n/a
3	ARID3A	chr1:246273822-246274255	K562	blood:	n/a	n/a
4	ARID3A	chr1:246339492-246340117	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:246274930-246275288	K562	blood:	n/a	n/a
6	ARID3A	chr1:246168514-246168540	K562	blood:	n/a	n/a
7	ARID3A	chr1:246351102-246351709	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:246306858-246307142	K562	blood:	n/a	n/a
9	ARID3A	chr1:246333485-246334689	K562	blood:	n/a	n/a
10	ARID3A	chr1:246166462-246166818	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:246339570-246339954	K562	blood:	n/a	n/a
12	ARID3A	chr1:246151994-246152588	K562	blood:	n/a	n/a
13	ARID3A	chr1:246305649-246306059	K562	blood:	n/a	n/a
14	ARID3A	chr1:246317239-246317589	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:246297019-246297023	K562	blood:	n/a	n/a
16	ARID3A	chr1:246175622-246175892	K562	blood:	n/a	n/a
17	ARID3A	chr1:246303129-246303329	HepG2	liver:	n/a	n/a
18	ARID3A	chr1:246378433-246378571	HepG2	liver:	n/a	n/a
19	ARID3A	chr1:246409804-246409947	K562	blood:	n/a	n/a
20	ARID3A	chr1:246383173-246383457	HepG2	liver:	n/a	n/a
21	ARID3A	chr1:246378134-246379212	K562	blood:	n/a	n/a
22	ARID3A	chr1:246232168-246232911	K562	blood:	n/a	n/a
23	ARID3A	chr1:246329377-246329956	K562	blood:	n/a	n/a
24	ARID3A	chr1:246332132-246332717	K562	blood:	n/a	n/a
25	ARID3A	chr1:246166458-246166858	K562	blood:	n/a	n/a
26	ARID3A	chr1:246254962-246255161	K562	blood:	n/a	n/a
27	ARID3A	chr1:246269535-246270147	K562	blood:	n/a	n/a
28	ARID3A	chr1:246276744-246277369	K562	blood:	n/a	n/a
29	ARID3A	chr1:246364034-246364381	K562	blood:	n/a	n/a
30	ARID3A	chr1:246268344-246268607	K562	blood:	n/a	n/a
31	ARID3A	chr1:246351173-246351659	K562	blood:	n/a	n/a
32	ARID3A	chr1:246303013-246303421	K562	blood:	n/a	n/a
33	ARID3A	chr1:246340416-246340426	K562	blood:	n/a	n/a
34	ARID3A	chr1:246345414-246346141	K562	blood:	n/a	n/a
35	ATF1	chr1:246378205-246378667	K562	blood:	n/a	n/a
36	ATF1	chr1:246276829-246277358	K562	blood:	n/a	n/a
37	ATF1	chr1:246273843-246274253	K562	blood:	n/a	n/a
38	ATF1	chr1:246317155-246317561	K562	blood:	n/a	n/a
39	ATF1	chr1:246280509-246280836	K562	blood:	n/a	n/a
40	ATF1	chr1:246269670-246270067	K562	blood:	n/a	n/a
41	ATF1	chr1:246333942-246334272	K562	blood:	n/a	n/a
42	ATF1	chr1:246332388-246332644	K562	blood:	n/a	n/a
43	ATF1	chr1:246363474-246363487	K562	blood:	n/a	n/a
44	ATF1	chr1:246241695-246242195	K562	blood:	n/a	n/a
45	ATF1	chr1:246149871-246150694	K562	blood:	n/a	n/a
46	ATF1	chr1:246316226-246316752	K562	blood:	n/a	n/a
47	ATF1	chr1:246304350-246304649	K562	blood:	n/a	n/a
48	ATF1	chr1:246376288-246376805	K562	blood:	n/a	n/a
49	ATF1	chr1:246284953-246285126	K562	blood:	n/a	n/a
50	ATF1	chr1:246254868-246255152	K562	blood:	n/a	n/a

(count:2626 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246414665-246414715	AG04450	lung:	fetal
2	chr1:246125159-246125209	HRE	kidney:	n/a
3	chr1:246310485-246310535	BE2_C	brain:	n/a
4	chr1:246414665-246414715	AG04450	lung:	fetal
5	chr1:246125159-246125209	HRE	kidney:	n/a
6	chr1:246310485-246310535	BE2_C	brain:	n/a
7	chr1:246231142-246231192	PFSK-1	brain:	n/a
8	chr1:246139198-246139248	ECC-1	luminal epithelium:	n/a
9	chr1:246370933-246370983	H1-hESC	embryonic stem cell:	embryo
10	chr1:246160640-246160690	HAEpiC	amniotic membrane:	n/a
11	chr1:246415214-246415264	ECC-1	luminal epithelium:	n/a
12	chr1:246383021-246383071	GM12892	blood:	n/a
13	chr1:246305399-246305449	SKMC	muscle:	n/a
14	chr1:246363660-246363710	HCPEpiC	choroid plexus:	n/a
15	chr1:246416688-246416738	ProgFib	skin:	n/a
16	chr1:246378510-246378560	HRE	kidney:	n/a
17	chr1:246140350-246140400	NHDF-neo	bronchial:	n/a
18	chr1:246415176-246415226	Jurkat	blood:	n/a
19	chr1:246370933-246370983	MCF10A-Er-Src	breast:	n/a
20	chr1:246139198-246139248	HAEpiC	amniotic membrane:	n/a
21	chr1:246305399-246305449	IMR90	lung:	fetal
22	chr1:246140350-246140400	HRCEpiC	kidney:	n/a
23	chr1:246235275-246235325	MCF-7	breast:	n/a
24	chr1:246363574-246363624	PrEC	prostate:	n/a
25	chr1:246139198-246139248	HIPEpiC	eye:	n/a
26	chr1:246231142-246231192	BE2_C	brain:	n/a
27	chr1:246363660-246363710	ECC-1	luminal epithelium:	n/a
28	chr1:246415176-246415226	AG04449	skin:	fetal
29	chr1:246415555-246415605	U87	brain:	n/a
30	chr1:246415555-246415605	NHDF-neo	bronchial:	n/a
31	chr1:246370933-246370983	HIPEpiC	eye:	n/a
32	chr1:246203591-246203641	HCF	heart:	n/a
33	chr1:246254215-246254265	HRCEpiC	kidney:	n/a
34	chr1:246231142-246231192	SKMC	muscle:	n/a
35	chr1:246414840-246414890	HCM	heart:	n/a
36	chr1:246172272-246172322	HCPEpiC	choroid plexus:	n/a
37	chr1:246254338-246254388	T-47D	breast:	n/a
38	chr1:246231142-246231192	SAEC	small airway:	n/a
39	chr1:246310349-246310399	HCPEpiC	choroid plexus:	n/a
40	chr1:246310349-246310399	HPAEpiC	pulmonary alveolar:	n/a
41	chr1:246172272-246172322	Jurkat	blood:	n/a
42	chr1:246363660-246363710	HNPCEpiC	eye:	n/a
43	chr1:246254283-246254333	HCF	heart:	n/a
44	chr1:246148901-246148951	GM19239	blood:	n/a
45	chr1:246304208-246304258	HIPEpiC	eye:	n/a
46	chr1:246132061-246132111	HCT-116	colon:	n/a
47	chr1:246172285-246172335	H1-hESC	embryonic stem cell:	embryo
48	chr1:246324811-246324861	HCPEpiC	choroid plexus:	n/a
49	chr1:246139198-246139248	ProgFib	skin:	n/a
50	chr1:246254283-246254333	Caco-2	colon:	n/a

(count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr1:246051737..246052708-chr1:246165978..246167068,4	MCF-7	breast:
2	chr1:246304167..246305671-chr1:246388175..246390464,2	K562	blood:
3	chr1:246126390..246128678-chr1:246132301..246134356,2	K562	blood:
4	chr1:246244386..246246974-chr1:246250751..246252687,2	K562	blood:
5	chr1:246323812..246327417-chr1:246344916..246347036,3	K562	blood:
6	chr1:246371493..246375018-chr1:246378492..246381970,3	MCF-7	breast:
7	chr1:246118130..246122848-chr1:246123381..246128902,9	K562	blood:
8	chr1:246357127..246361362-chr1:246362304..246364273,3	K562	blood:
9	chr1:246171457..246174001-chr1:246174908..246177253,2	K562	blood:
10	chr1:246218695..246221099-chr1:246227614..246229806,2	K562	blood:
11	chr1:246129359..246131604-chr1:246142419..246144141,2	K562	blood:
12	chr1:246297778..246300991-chr1:246304218..246307827,5	K562	blood:
13	chr1:246285178..246287872-chr1:246288956..246290649,2	K562	blood:
14	chr1:246192575..246194400-chr1:246202889..246205782,2	K562	blood:
15	chr1:246290308..246292260-chr1:246292808..246295373,2	K562	blood:
16	chr1:246303120..246308295-chr1:246314639..246320743,10	K562	blood:
17	chr1:246331853..246336135-chr1:246348494..246351528,4	K562	blood:
18	chr1:246193638..246196083-chr1:246198035..246200381,2	K562	blood:
19	chr1:246131436..246134219-chr1:246149088..246150607,2	K562	blood:
20	chr1:246189669..246191327-chr1:246194345..246196797,2	K562	blood:
21	chr1:246175270..246176065-chr1:246443608..246444506,2	MCF-7	breast:
22	chr1:246093581..246095497-chr1:246148758..246151121,2	K562	blood:
23	chr1:246262654..246264469-chr1:246272321..246273994,2	K562	blood:
24	chr1:246389393..246391368-chr1:246392967..246394891,2	K562	blood:
25	chr1:246279918..246282776-chr1:246284778..246286908,2	K562	blood:
26	chr1:246385164..246386821-chr1:246393908..246395594,2	K562	blood:
27	chr1:246297714..246299479-chr1:246301479..246303865,2	MCF-7	breast:
28	chr1:246353361..246355066-chr1:246367112..246369364,2	K562	blood:
29	chr1:246313570..246315182-chr1:246317792..246320324,2	K562	blood:
30	chr1:246237075..246239017-chr1:246241942..246243808,2	K562	blood:
31	chr1:246286174..246287745-chr1:246302664..246304849,2	K562	blood:
32	chr1:246129149..246130792-chr1:246136104..246138621,2	K562	blood:
33	chr1:246355633..246357976-chr1:246377083..246378948,2	K562	blood:
34	chr1:246254942..246257764-chr1:246259415..246261815,3	K562	blood:
35	chr1:246304167..246305671-chr1:246388175..246390464,2	K562	blood:
36	chr1:246273236..246275581-chr1:246292847..246295788,2	K562	blood:
37	chr1:246130619..246132818-chr1:246134043..246137611,3	K562	blood:
38	chr1:246284694..246286450-chr1:246289366..246291707,2	MCF-7	breast:
39	chr1:246261134..246264107-chr1:246270558..246273069,4	K562	blood:
40	chr1:246308927..246313479-chr1:246313623..246318049,5	K562	blood:
41	chr1:246175573..246176199-chr1:246409475..246409997,2	K562	blood:
42	chr1:246323812..246327417-chr1:246344916..246347036,3	K562	blood:
43	chr1:246242761..246244330-chr1:246271984..246274792,2	K562	blood:
44	chr1:246377128..246379304-chr1:246383039..246386771,4	K562	blood:
45	chr1:246174027..246176471-chr1:246609850..246611898,2	K562	blood:
46	chr1:246377070..246379889-chr1:246380725..246383126,2	MCF-7	breast:
47	chr1:246175301..246176197-chr1:246366037..246366781,3	MCF-7	breast:
48	chr1:246303201..246305225-chr1:246319673..246321317,2	MCF-7	breast:
49	chr1:246345857..246348884-chr1:246378191..246381575,3	K562	blood:
50	chr1:246272101..246273950-chr1:246817056..246818596,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF26B-2	chr1:246271928-246272019	ENSG00000226876.1
2	lnc-KIF26B-1	chr1:246198521-246198905	ENSG00000235096.1
3	lnc-KIF26B-2	chr1:246273081-246273195	NONHSAT010700
4	lnc-KIF26B-2	chr1:246274633-246274883	NONHSAT010700
5	lnc-KIF26B-1	chr1:246197785-246197936	ENSG00000235096.1
6	lnc-KIF26B-1	chr1:246196853-246197018	ENSG00000235096.1
7	lnc-KIF26B-2	chr1:246274633-246274831	ENSG00000226876.1
8	lnc-KIF26B-2	chr1:246276989-246277108	ENSG00000226876.1
9	lnc-CNST-4	chr1:246342080-246342506	NONHSAT010702
10	lnc-KIF26B-2	chr1:246274628-246274831	ENSG00000226876.1
11	lnc-KIF26B-2	chr1:246276991-246277168	ENSG00000226876.1
12	lnc-KIF26B-2	chr1:246273084-246273195	ENSG00000226876.1

No data

Variant related genes	Relation type
ENSG00000226876	TF binding region
ENSG00000235096	TF binding region
CHCHD4P5	TF binding region
SMYD3	TF binding region
RNU6-1283P	TF binding region
ENSG00000226876	CpG island
ENSG00000235096	CpG island
CHCHD4P5	CpG island
SMYD3	CpG island
RNU6-1283P	CpG island
ENSG00000185420	chromatin interactions
ENSG00000202184	chromatin interactions
ENSG00000235096	chromatin interactions
ENSG00000226876	chromatin interactions

Extended variants
information (count: 13468 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:13468 , 50 per page) page: 1 2 3 4 5 6 7 ... 270

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1544151	chr1:246122871-246122872	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113370009	chr1:246122881-246122882	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs151030105	chr1:246122882-246122883	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184439885	chr1:246122895-246122896	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563166901	chr1:246122971-246122972	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4323674	chr1:246122973-246122974	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs548580975	chr1:246122979-246122980	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368321896	chr1:246123161-246123162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10924405	chr1:246123195-246123196	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs189208852	chr1:246123220-246123221	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139709948	chr1:246123242-246123243	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539245541	chr1:246123270-246123271	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549994128	chr1:246123297-246123298	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10924406	chr1:246123308-246123309	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs570079452	chr1:246123349-246123350	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200414066	chr1:246123351-246123352	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61839378	chr1:246123368-246123369	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571681721	chr1:246123377-246123378	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149848855	chr1:246123431-246123432	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs372762923	chr1:246123443-246123444	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557529455	chr1:246123457-246123458	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs376244725	chr1:246123467-246123468	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs4233248	chr1:246123475-246123476	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546078910	chr1:246123507-246123508	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116868772	chr1:246123550-246123551	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs544492805	chr1:246123608-246123609	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563103181	chr1:246123615-246123616	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs182210749	chr1:246123639-246123640	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544775694	chr1:246123673-246123674	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs529875837	chr1:246123675-246123676	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs371697333	chr1:246123683-246123684	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs145889358	chr1:246123714-246123715	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533841065	chr1:246123772-246123773	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs186484676	chr1:246123788-246123789	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149007638	chr1:246123789-246123790	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11799836	chr1:246123796-246123797	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564419219	chr1:246123854-246123855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs11576780	chr1:246123861-246123862	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191171162	chr1:246123890-246123891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569482770	chr1:246123964-246123965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529078046	chr1:246124004-246124005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528570073	chr1:246124010-246124011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs565649213	chr1:246124024-246124025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs112492723	chr1:246124029-246124030	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546706067	chr1:246124030-246124031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs61051860	chr1:246124054-246124055	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114429250	chr1:246124102-246124103	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146611206	chr1:246124112-246124113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs571233218	chr1:246124141-246124142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181526635	chr1:246124146-246124147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246103800-246132600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:246112600-246127400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:246112600-246132000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:246117800-246123600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:246118000-246124400	Weak transcription	Fetal Kidney	kidney
6	chr1:246118000-246132200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:246118000-246132200	Weak transcription	Psoas Muscle	Psoas
8	chr1:246118200-246123200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:246118200-246132600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:246120000-246125000	Weak transcription	Placenta	Placenta
11	chr1:246120200-246123600	Weak transcription	Osteobl	bone
12	chr1:246120200-246124400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr1:246120400-246123400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr1:246120400-246124000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:246120400-246124200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:246121000-246166200	Weak transcription	Primary T cells from cord blood	blood
17	chr1:246122000-246124400	Weak transcription	Fetal Stomach	stomach
18	chr1:246122400-246132000	Weak transcription	HSMM	muscle
19	chr1:246122800-246123000	ZNF genes & repeats	GM12878-XiMat	blood
20	chr1:246122800-246123800	Strong transcription	K562	blood
21	chr1:246123200-246125400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:246123400-246124800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr1:246123600-246124000	Enhancers	Osteobl	bone
24	chr1:246123600-246125400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:246123800-246124400	Weak transcription	K562	blood
26	chr1:246124000-246125000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:246124200-246124800	Enhancers	NHLF	lung
28	chr1:246124200-246125200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:246124400-246125400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:246124400-246125400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:246124400-246125400	Enhancers	Fetal Kidney	kidney
32	chr1:246124400-246125400	Enhancers	Fetal Stomach	stomach
33	chr1:246124400-246125400	Enhancers	HSMMtube	muscle
34	chr1:246124400-246125600	Enhancers	K562	blood
35	chr1:246124400-246125600	Enhancers	NHDF-Ad	bronchial
36	chr1:246124400-246125800	Enhancers	Fetal Lung	lung
37	chr1:246124800-246125400	Enhancers	Fetal Heart	heart
38	chr1:246124800-246132000	Weak transcription	NHLF	lung
39	chr1:246125000-246125800	Enhancers	Placenta	Placenta
40	chr1:246125400-246127400	Weak transcription	Fetal Kidney	kidney
41	chr1:246125400-246132000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:246125600-246126000	Enhancers	Ovary	ovary
43	chr1:246125600-246130600	Weak transcription	K562	blood
44	chr1:246125800-246133800	Weak transcription	Placenta	Placenta
45	chr1:246126000-246127000	Weak transcription	Ovary	ovary
46	chr1:246126000-246127800	Enhancers	HepG2	liver
47	chr1:246126400-246127600	Weak transcription	Aorta	Aorta
48	chr1:246127000-246127200	Enhancers	Ovary	ovary
49	chr1:246127200-246127600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:246127400-246127600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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