Variant report

Variant	nsv898370
Chromosome Location	chr11:107027991-107430300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1777)
CpG islands
(count:1222)
Chromatin interactive
region (count:100)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:107298390-107298697	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:107401280-107401282	K562	blood:	n/a	n/a
3	ARID3A	chr11:107279204-107280430	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:107068416-107069073	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:107067338-107067971	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:107298678-107298818	K562	blood:	n/a	n/a
7	ARID3A	chr11:107114621-107115003	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:107256191-107256678	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:107420016-107420307	K562	blood:	n/a	n/a
10	ARID3A	chr11:107372561-107372562	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:107328280-107328788	HepG2	liver:	n/a	n/a
12	ARID3A	chr11:107125887-107126018	K562	blood:	n/a	n/a
13	ARID3A	chr11:107028240-107028924	HepG2	liver:	n/a	n/a
14	ARID3A	chr11:107073929-107074099	HepG2	liver:	n/a	n/a
15	ARID3A	chr11:107328127-107328887	K562	blood:	n/a	n/a
16	ARID3A	chr11:107073226-107073508	HepG2	liver:	n/a	n/a
17	ATF1	chr11:107328463-107328763	K562	blood:	n/a	n/a
18	ATF1	chr11:107119900-107120053	K562	blood:	n/a	n/a
19	ATF1	chr11:107240708-107240809	K562	blood:	n/a	n/a
20	ATF1	chr11:107118328-107118368	K562	blood:	n/a	n/a
21	ATF1	chr11:107359188-107359352	K562	blood:	n/a	n/a
22	ATF1	chr11:107298560-107298761	K562	blood:	n/a	n/a
23	ATF1	chr11:107411871-107411961	K562	blood:	n/a	n/a
24	ATF2	chr11:107419878-107420193	GM12878	blood:	n/a	n/a
25	ATF2	chr11:107328307-107328946	GM12878	blood:	n/a	n/a
26	ATF2	chr11:107241054-107241483	GM12878	blood:	n/a	n/a
27	ATF3	chr11:107328243-107328841	HepG2	liver:	n/a	n/a
28	ATF3	chr11:107328369-107328693	GM12878	blood:	n/a	n/a
29	ATF3	chr11:107328335-107328738	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr11:107328396-107328669	HepG2	liver:	n/a	n/a
31	ATF3	chr11:107328394-107328774	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr11:107328375-107328670	K562	blood:	n/a	n/a
33	ATF3	chr11:107328251-107328813	GM12878	blood:	n/a	n/a
34	BACH1	chr11:107267990-107268348	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr11:107161599-107161648	K562	blood:	n/a	n/a
36	BATF	chr11:107134920-107135143	GM12878	blood:	n/a	chr11:107134970-107134980
37	BHLHE40	chr11:107328231-107328803	K562	blood:	n/a	n/a
38	BHLHE40	chr11:107120661-107120879	K562	blood:	n/a	n/a
39	BHLHE40	chr11:107298617-107298890	K562	blood:	n/a	n/a
40	BHLHE40	chr11:107419983-107420258	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:107123579-107123932	K562	blood:	n/a	n/a
42	BHLHE40	chr11:107123612-107123903	GM12878	blood:	n/a	n/a
43	BHLHE40	chr11:107125712-107125922	K562	blood:	n/a	n/a
44	BHLHE40	chr11:107279399-107279754	HepG2	liver:	n/a	n/a
45	BHLHE40	chr11:107130509-107130831	K562	blood:	n/a	n/a
46	BRCA1	chr11:107328002-107328799	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr11:107419931-107420449	HCT-116	colon:	n/a	n/a
48	CBX3	chr11:107389244-107389485	K562	blood:	n/a	n/a
49	CBX3	chr11:107363833-107364256	HCT-116	colon:	n/a	n/a
50	CBX3	chr11:107328281-107328798	K562	blood:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107328671-107328721	GM06990	blood:	n/a
2	chr11:107232729-107232779	HPAEpiC	pulmonary alveolar:	n/a
3	chr11:107328671-107328721	GM06990	blood:	n/a
4	chr11:107232729-107232779	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:107328690-107328740	AoSMC	blood vessel:	n/a
6	chr11:107328559-107328609	NH-A	brain:	n/a
7	chr11:107328442-107328492	K562	blood:	n/a
8	chr11:107328559-107328609	AoSMC	blood vessel:	n/a
9	chr11:107328605-107328655	AG09309	skin:	n/a
10	chr11:107324751-107324801	HCT-116	colon:	n/a
11	chr11:107328442-107328492	AG10803	skin:	n/a
12	chr11:107047494-107047544	HCPEpiC	choroid plexus:	n/a
13	chr11:107047888-107047938	AG09309	skin:	n/a
14	chr11:107047494-107047544	HepG2	liver:	n/a
15	chr11:107328690-107328740	HL-60	blood:	n/a
16	chr11:107044383-107044433	HCT-116	colon:	n/a
17	chr11:107328559-107328609	PFSK-1	brain:	n/a
18	chr11:107243587-107243637	SKMC	muscle:	n/a
19	chr11:107328914-107328964	GM12891	blood:	n/a
20	chr11:107326471-107326521	NT2-D1	testis:	n/a
21	chr11:107328605-107328655	NHDF-neo	bronchial:	n/a
22	chr11:107044383-107044433	HCF	heart:	n/a
23	chr11:107328671-107328721	GM12892	blood:	n/a
24	chr11:107047494-107047544	ProgFib	skin:	n/a
25	chr11:107048184-107048234	GM06990	blood:	n/a
26	chr11:107328586-107328636	SK-N-MC	brain:	n/a
27	chr11:107328586-107328636	IMR90	lung:	fetal
28	chr11:107328914-107328964	NHDF-neo	bronchial:	n/a
29	chr11:107328605-107328655	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:107044383-107044433	GM12891	blood:	n/a
31	chr11:107047494-107047544	NHDF-neo	bronchial:	n/a
32	chr11:107324751-107324801	HUVEC	blood vessel:	n/a
33	chr11:107328586-107328636	Hela-S3	cervix:	n/a
34	chr11:107328605-107328655	AG04449	skin:	fetal
35	chr11:107328914-107328964	A549	lung:	n/a
36	chr11:107324751-107324801	GM12891	blood:	n/a
37	chr11:107328586-107328636	BE2_C	brain:	n/a
38	chr11:107328442-107328492	SAEC	small airway:	n/a
39	chr11:107331110-107331160	MCF10A-Er-Src	breast:	n/a
40	chr11:107328914-107328964	SK-N-SH	brain:	n/a
41	chr11:107243587-107243637	Jurkat	blood:	n/a
42	chr11:107326471-107326521	HCF	heart:	n/a
43	chr11:107328657-107328707	NH-A	brain:	n/a
44	chr11:107328442-107328492	HepG2	liver:	n/a
45	chr11:107420502-107420552	AG09319	gingival:	n/a
46	chr11:107328605-107328655	NH-A	brain:	n/a
47	chr11:107328636-107328686	HNPCEpiC	eye:	n/a
48	chr11:107328525-107328575	HRCEpiC	kidney:	n/a
49	chr11:107328525-107328575	GM06990	blood:	n/a
50	chr11:107328442-107328492	HRPEpiC	eye:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:107237489..107239255-chr11:107241546..107243344,2	K562	blood:
2	chr11:107081384..107083481-chr11:107086943..107088953,2	K562	blood:
3	chr11:107108368..107111074-chr11:107113381..107114991,2	K562	blood:
4	chr11:107399887..107402432-chr11:107404521..107406655,2	K562	blood:
5	chr11:107284097..107287065-chr11:107292500..107294611,2	MCF-7	breast:
6	chr11:107411230..107412987-chr11:107414940..107417572,2	K562	blood:
7	chr11:107316142..107319127-chr11:107320782..107322583,2	K562	blood:
8	chr11:107317031..107320685-chr11:107326705..107328538,3	K562	blood:
9	chr11:107265232..107267832-chr11:107267875..107270757,2	K562	blood:
10	chr11:107297886..107300140-chr11:107301084..107303948,2	K562	blood:
11	chr11:107069683..107071743-chr11:107086703..107088900,2	K562	blood:
12	chr11:107096224..107098662-chr11:107099428..107101008,2	K562	blood:
13	chr11:107402166..107405031-chr11:107412950..107414876,2	K562	blood:
14	chr11:107342962..107345043-chr11:107346726..107348566,2	K562	blood:
15	chr11:107402166..107405031-chr11:107412950..107414876,2	K562	blood:
16	chr11:107292984..107295950-chr11:107297622..107299672,2	K562	blood:
17	chr11:107285740..107288014-chr11:107318312..107321068,2	K562	blood:
18	chr11:107405244..107407798-chr11:107410887..107412865,2	K562	blood:
19	chr11:107096224..107098662-chr11:107099428..107101008,2	K562	blood:
20	chr11:107173736..107175485-chr11:107175928..107178317,2	K562	blood:
21	chr11:107405244..107407798-chr11:107410887..107412865,2	K562	blood:
22	chr1:28908024..28908798-chr11:107328064..107328889,2	HCT-116	colon:
23	chr11:107374400..107376459-chr11:107377850..107380613,2	K562	blood:
24	chr11:107298284..107300612-chr11:107304027..107305588,2	K562	blood:
25	chr11:107317620..107320783-chr11:107322990..107325407,3	K562	blood:
26	chr11:107265232..107267832-chr11:107267875..107270757,2	K562	blood:
27	chr11:107241951..107244732-chr11:107327122..107328857,2	K562	blood:
28	chr11:107321712..107323606-chr11:107324966..107327081,2	K562	blood:
29	chr11:107258832..107260455-chr11:107266741..107268577,2	K562	blood:
30	chr11:107420177..107420684-chr11:107560050..107560867,2	MCF-7	breast:
31	chr11:107213050..107215630-chr11:107219007..107221031,2	K562	blood:
32	chr11:107321719..107323399-chr11:107326158..107328000,2	MCF-7	breast:
33	chr11:107311896..107313858-chr11:107327138..107329604,2	K562	blood:
34	chr11:107114259..107116985-chr11:107121608..107123484,2	K562	blood:
35	chr11:107297886..107300140-chr11:107301084..107303948,2	K562	blood:
36	chr11:107317031..107320685-chr11:107326705..107328538,3	K562	blood:
37	chr11:107123368..107125286-chr11:107129770..107131910,2	K562	blood:
38	chr11:107114259..107116985-chr11:107121608..107123484,2	K562	blood:
39	chr11:107317620..107320783-chr11:107322990..107325407,3	K562	blood:
40	chr11:107311896..107313858-chr11:107327138..107329604,2	K562	blood:
41	chr11:107282183..107285508-chr11:107287409..107291356,4	K562	blood:
42	chr11:107290994..107293212-chr11:107294451..107296538,3	K562	blood:
43	chr11:107423484..107425068-chr11:107427739..107430641,2	K562	blood:
44	chr11:107240491..107241393-chr16:2244600..2245300,2	MCF-7	breast:
45	chr11:107316142..107319127-chr11:107320782..107322583,2	K562	blood:
46	chr11:107402012..107404906-chr11:107408534..107410570,3	K562	blood:
47	chr11:107282787..107285508-chr11:107287917..107290011,2	K562	blood:
48	chr11:107282183..107285508-chr11:107287409..107291356,4	K562	blood:
49	chr11:107258832..107260455-chr11:107266741..107268577,2	K562	blood:
50	chr11:107321712..107323606-chr11:107324966..107327081,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CWF19L2-1	chr11:107182073-107186290	XLOC_009544
2	lnc-CWF19L2-1	chr11:107183057-107184045	NONHSAT023993
3	lnc-CWF19L2-1	chr11:107182858-107186997	ENSG00000261098.1
4	lnc-CWF19L2-1	chr11:107184094-107184136	NONHSAT023993
5	lnc-CWF19L2-1	chr11:107184592-107184806	NONHSAT023993
6	lnc-CWF19L2-2	chr11:107384618-107385205	predAs_engstrom06_BG031574_1
7	lnc-CWF19L2-1	chr11:107181806-107181958	XLOC_009544

No data

Variant related genes	Relation type
ENSG00000261098	TF binding region
SMARCE1P1	TF binding region
ENSG00000255353	TF binding region
CWF19L2	TF binding region
ENSG00000261098	CpG island
SMARCE1P1	CpG island
ENSG00000255353	CpG island
CWF19L2	CpG island
ENSG00000137760	chromatin interactions
ENSG00000152404	chromatin interactions
ENSG00000101384	chromatin interactions
ENSG00000197989	chromatin interactions

Extended variants
information (count: 12819 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:12819 , 50 per page) page: 1 2 3 4 5 6 7 ... 257

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2014174	chr11:107027991-107027992	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374118466	chr11:107028024-107028025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577624849	chr11:107028115-107028116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557221553	chr11:107028128-107028129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560510704	chr11:107028256-107028257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373183050	chr11:107028262-107028263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544047876	chr11:107028288-107028289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186454483	chr11:107028315-107028316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs59193304	chr11:107028316-107028317	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs561536348	chr11:107028323-107028324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532551011	chr11:107028418-107028419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189636060	chr11:107028450-107028451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145479237	chr11:107028466-107028467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182319744	chr11:107028477-107028478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532499247	chr11:107028492-107028493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547913264	chr11:107028500-107028501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114156421	chr11:107028508-107028509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534022183	chr11:107028552-107028553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555165670	chr11:107028563-107028564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187862278	chr11:107028611-107028612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191427396	chr11:107028620-107028621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555693234	chr11:107028629-107028630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577606822	chr11:107028664-107028665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151194530	chr11:107028680-107028681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553924036	chr11:107028705-107028706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76339452	chr11:107028722-107028723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572067027	chr11:107028730-107028731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183248950	chr11:107028737-107028738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368216101	chr11:107028753-107028754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1425239	chr11:107028754-107028755	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs116194464	chr11:107028764-107028765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565128958	chr11:107028813-107028814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532575999	chr11:107028814-107028815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547552542	chr11:107028853-107028854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559771570	chr11:107028879-107028880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530151501	chr11:107028893-107028894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140339541	chr11:107028905-107028906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188612819	chr11:107028913-107028914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150365427	chr11:107028932-107028933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145094168	chr11:107028954-107028955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553240423	chr11:107028961-107028962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78828639	chr11:107028966-107028967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528228005	chr11:107029062-107029063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192334996	chr11:107029070-107029071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73544891	chr11:107029079-107029080	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs116679051	chr11:107029129-107029130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75417331	chr11:107029130-107029131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555195933	chr11:107029143-107029144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576753741	chr11:107029157-107029158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11530514	chr11:107029182-107029183	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	21811512	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164920	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:4598 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107027400-107028400	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr11:107027400-107028800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr11:107027400-107029000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr11:107027400-107029600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr11:107027800-107028400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr11:107027800-107028600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr11:107027800-107028800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr11:107027800-107029200	Enhancers	HepG2	liver
9	chr11:107027800-107030200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr11:107027800-107030200	Enhancers	Liver	Liver
11	chr11:107028000-107028400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:107028000-107032200	Enhancers	Adipose Nuclei	Adipose
13	chr11:107028400-107029000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:107028600-107030000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr11:107029000-107029600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:107029600-107030400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:107029600-107030600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr11:107030000-107030600	Enhancers	HMEC	breast
19	chr11:107030800-107031000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:107039400-107043400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr11:107043200-107044600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:107043400-107043800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr11:107043400-107044000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr11:107043400-107044000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr11:107043400-107044000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr11:107043400-107044000	Enhancers	Placenta Amnion	Placenta Amnion
27	chr11:107043400-107044200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr11:107043400-107044600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:107043600-107044000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr11:107043600-107044000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr11:107043600-107044000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:107048400-107049000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr11:107050600-107051400	Enhancers	Adipose Nuclei	Adipose
34	chr11:107050600-107051800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:107053400-107053800	Enhancers	NH-A	brain
36	chr11:107053800-107055000	Weak transcription	NH-A	brain
37	chr11:107054600-107055400	Enhancers	Fetal Brain Female	brain
38	chr11:107054600-107056400	Enhancers	Fetal Brain Male	brain
39	chr11:107054800-107055200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr11:107054800-107056000	Enhancers	Fetal Lung	lung
41	chr11:107055000-107055200	Enhancers	NH-A	brain
42	chr11:107063800-107064000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:107063800-107064000	ZNF genes & repeats	Left Ventricle	heart
44	chr11:107067000-107069400	Enhancers	HepG2	liver
45	chr11:107067200-107067400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:107067200-107069200	Enhancers	A549	lung
47	chr11:107067600-107068000	Enhancers	Fetal Intestine Large	intestine
48	chr11:107067600-107068200	Enhancers	Liver	Liver
49	chr11:107068200-107072400	Weak transcription	Liver	Liver
50	chr11:107069000-107072800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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