Variant report

Variant	nsv1037810
Chromosome Location	chr11:67510614-67736481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3253)
CpG islands
(count:1468)
Chromatin interactive
region (count:12)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3253 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:67546855-67547018	K562	blood:	n/a	n/a
2	ATF1	chr11:67572955-67573090	K562	blood:	n/a	n/a
3	ATF1	chr11:67525774-67525796	K562	blood:	n/a	n/a
4	ATF3	chr11:67593917-67594176	K562	blood:	n/a	n/a
5	ATF3	chr11:67723227-67723408	K562	blood:	n/a	chr11:67723283-67723292
6	BACH1	chr11:67723212-67723405	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr11:67548940-67549181	GM12878	blood:	n/a	chr11:67549020-67549031
8	BATF	chr11:67647999-67648547	GM12878	blood:	n/a	n/a
9	BATF	chr11:67548820-67549170	GM12878	blood:	n/a	chr11:67549020-67549031
10	BATF	chr11:67571884-67572418	GM12878	blood:	n/a	chr11:67572041-67572051
11	BATF	chr11:67697656-67698323	GM12878	blood:	n/a	n/a
12	BATF	chr11:67627161-67627468	GM12878	blood:	n/a	n/a
13	BATF	chr11:67574662-67574949	GM12878	blood:	n/a	n/a
14	BATF	chr11:67615409-67615586	GM12878	blood:	n/a	n/a
15	BATF	chr11:67675477-67675829	GM12878	blood:	n/a	n/a
16	BATF	chr11:67555151-67555449	GM12878	blood:	n/a	n/a
17	BATF	chr11:67571990-67572187	GM12878	blood:	n/a	chr11:67572041-67572051
18	BATF	chr11:67559731-67559980	GM12878	blood:	n/a	n/a
19	BATF	chr11:67644809-67645315	GM12878	blood:	n/a	chr11:67645088-67645096
20	BATF	chr11:67556628-67556900	GM12878	blood:	n/a	n/a
21	BATF	chr11:67646855-67647126	GM12878	blood:	n/a	n/a
22	BATF	chr11:67648616-67648960	GM12878	blood:	n/a	n/a
23	BATF	chr11:67697714-67698270	GM12878	blood:	n/a	n/a
24	BATF	chr11:67644982-67645399	GM12878	blood:	n/a	chr11:67645088-67645096
25	BATF	chr11:67675453-67675797	GM12878	blood:	n/a	n/a
26	BATF	chr11:67555087-67555437	GM12878	blood:	n/a	n/a
27	BATF	chr11:67667021-67667379	GM12878	blood:	n/a	n/a
28	BATF	chr11:67572577-67572827	GM12878	blood:	n/a	n/a
29	BATF	chr11:67627170-67627405	GM12878	blood:	n/a	n/a
30	BATF	chr11:67652428-67652731	GM12878	blood:	n/a	n/a
31	BATF	chr11:67606914-67607130	GM12878	blood:	n/a	n/a
32	BATF	chr11:67567330-67567611	GM12878	blood:	n/a	n/a
33	BATF	chr11:67651682-67652098	GM12878	blood:	n/a	n/a
34	BATF	chr11:67706536-67706734	GM12878	blood:	n/a	n/a
35	BATF	chr11:67646832-67647124	GM12878	blood:	n/a	n/a
36	BATF	chr11:67648065-67648547	GM12878	blood:	n/a	n/a
37	BATF	chr11:67651724-67652105	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:67675592-67675748	GM12878	blood:	n/a	chr11:67675704-67675713
39	BCL11A	chr11:67627101-67627451	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:67697951-67698286	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:67559808-67560040	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:67645219-67645410	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:67710026-67710227	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:67648648-67648946	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:67559730-67560046	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:67651645-67652101	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:67572576-67572779	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:67675558-67675816	GM12878	blood:	n/a	chr11:67675704-67675713
49	BCL11A	chr11:67551659-67551843	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:67647974-67648564	GM12878	blood:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67572729-67572779	A549	lung:	n/a
2	chr11:67733632-67733682	AoSMC	blood vessel:	n/a
3	chr11:67572988-67573038	PrEC	prostate:	n/a
4	chr11:67726637-67726687	HMEC	breast:	n/a
5	chr11:67572729-67572779	A549	lung:	n/a
6	chr11:67733632-67733682	AoSMC	blood vessel:	n/a
7	chr11:67572988-67573038	PrEC	prostate:	n/a
8	chr11:67726637-67726687	HMEC	breast:	n/a
9	chr11:67571294-67571344	Jurkat	blood:	n/a
10	chr11:67734916-67734966	IMR90	lung:	fetal
11	chr11:67572716-67572766	RPTEC	kidney:	n/a
12	chr11:67722745-67722795	HCF	heart:	n/a
13	chr11:67726637-67726687	RPTEC	kidney:	n/a
14	chr11:67573741-67573791	PANC-1	pancreas:	n/a
15	chr11:67723411-67723461	GM12878	blood:	n/a
16	chr11:67577512-67577562	K562	blood:	n/a
17	chr11:67656390-67656440	Jurkat	blood:	n/a
18	chr11:67572999-67573049	HCF	heart:	n/a
19	chr11:67733632-67733682	HRPEpiC	eye:	n/a
20	chr11:67719813-67719863	Caco-2	colon:	n/a
21	chr11:67572988-67573038	T-47D	breast:	n/a
22	chr11:67574013-67574063	GM12891	blood:	n/a
23	chr11:67722909-67722959	LNCaP	prostate:	n/a
24	chr11:67653560-67653610	SK-N-SH	brain:	n/a
25	chr11:67572988-67573038	Hepatocyte	liver:	n/a
26	chr11:67572729-67572779	HIPEpiC	eye:	n/a
27	chr11:67726637-67726687	HCF	heart:	n/a
28	chr11:67719813-67719863	NB4	blood:	n/a
29	chr11:67573103-67573153	HUVEC	blood vessel:	n/a
30	chr11:67577512-67577562	CMK	blood:	n/a
31	chr11:67572988-67573038	NB4	blood:	n/a
32	chr11:67733632-67733682	ovcar-3	ovarian:	n/a
33	chr11:67573741-67573791	ECC-1	luminal epithelium:	n/a
34	chr11:67733632-67733682	HUVEC	blood vessel:	n/a
35	chr11:67572716-67572766	HRE	kidney:	n/a
36	chr11:67719813-67719863	GM12878	blood:	n/a
37	chr11:67571294-67571344	AG04449	skin:	fetal
38	chr11:67653560-67653610	SK-N-MC	brain:	n/a
39	chr11:67656390-67656440	HL-60	blood:	n/a
40	chr11:67572729-67572779	U87	brain:	n/a
41	chr11:67574013-67574063	ECC-1	luminal epithelium:	n/a
42	chr11:67722909-67722959	NH-A	brain:	n/a
43	chr11:67723411-67723461	AG04450	lung:	fetal
44	chr11:67572988-67573038	HAEpiC	amniotic membrane:	n/a
45	chr11:67572999-67573049	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:67572714-67572764	NHDF-neo	bronchial:	n/a
47	chr11:67577512-67577562	BJ	skin:	n/a
48	chr11:67572729-67572779	SK-N-SH_RA	brain:	n/a
49	chr11:67573741-67573791	K562	blood:	n/a
50	chr11:67577512-67577562	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:8938391..8938936-chr11:67572724..67573509,2	Hela-S3	cervix:
2	chr11:67395020..67397974-chr11:67571574..67573157,2	MCF-7	breast:
3	chr11:67572608..67573347-chr4:3956745..3957344,2	Hela-S3	cervix:
4	chr11:67571227..67572733-chr3:125634522..125636253,2	MCF-7	breast:
5	chr11:67396168..67397948-chr11:67571471..67573438,2	K562	blood:
6	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
7	chr11:67349032..67351635-chr11:67571367..67573562,2	K562	blood:
8	chr11:67722873..67723411-chr8:12516978..12517495,2	MCF-7	breast:
9	chr11:67615533..67616044-chr11:67722872..67723766,2	K562	blood:
10	chr1:150551803..150552520-chr11:67572791..67573460,2	Hela-S3	cervix:
11	chr11:67407400..67409857-chr11:67556404..67559360,2	MCF-7	breast:
12	chr11:67615533..67616044-chr11:67722872..67723766,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93B1-8	chr11:67679200-67679534	expReg_chr11_6588_-
2	lnc-UNC93B1-3	chr11:67704246-67704462	ENSG00000254610
3	lnc-NDUFS8-2	chr11:67653124-67653308	l_505_chr11:67645566-67653308_testes
4	lnc-NDUFV1-7	chr11:67511793-67512116	NONHSAT022465
5	lnc-NDUFS8-2	chr11:67645965-67646246	l_505_chr11:67645566-67653308_testes
6	lnc-NDUFS8-2	chr11:67654222-67654559	l_505_chr11:67645566-67653308_testes
7	lnc-NDUFS8-2	chr11:67655624-67655795	ENSG00000251637
8	lnc-NDUFV1-2	chr11:67544666-67545111	ENSG00000248509
9	lnc-UNC93B1-3	chr11:67702034-67702179	ENSG00000254610
10	lnc-NDUFV1-2	chr11:67547802-67550430	ENSG00000248509
11	lnc-NDUFS8-2	chr11:67673481-67673821	ENSG00000251637
12	lnc-NDUFS8-2	chr11:67653484-67654125	l_505_chr11:67645566-67653308_testes
13	lnc-NDUFS8-6	chr11:67703029-67703397	NONHSAT022485
14	lnc-NDUFS8-2	chr11:67654932-67654973	XLOC_009181
15	lnc-NDUFS8-2	chr11:67661350-67661552	XLOC_009181
16	lnc-NDUFS8-2	chr11:67645567-67645953	l_505_chr11:67645566-67653308_testes
17	lnc-NDUFS8-2	chr11:67653917-67654160	XLOC_009181
18	lnc-NDUFS8-2	chr11:67654061-67654160	ENSG00000251637
19	lnc-NDUFS8-2	chr11:67655621-67655795	XLOC_009181
20	lnc-UNC93B1-3	chr11:67707154-67707245	ENSG00000254610

No data

Variant related genes	Relation type
ENSG00000221553	TF binding region
ENSG00000251637	TF binding region
ENSG00000255147	TF binding region
ALG1L8P	TF binding region
RNU6-46P	TF binding region
RPS3AP40	TF binding region
FAM86C2P	TF binding region
ENSG00000254792	TF binding region
ENSG00000254610	TF binding region
ENSG00000254883	TF binding region
ENSG00000255230	TF binding region
ENSG00000254850	TF binding region
ENSG00000221553	CpG island
ENSG00000251637	CpG island
ENSG00000255147	CpG island
ALG1L8P	CpG island
RNU6-46P	CpG island
RPS3AP40	CpG island
FAM86C2P	CpG island
ENSG00000254792	CpG island
ENSG00000254610	CpG island
ENSG00000254883	CpG island
ENSG00000255230	CpG island
ENSG00000254850	CpG island
ENSG00000167799	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000084207	chromatin interactions
ENSG00000171084	chromatin interactions
ABTB1	miRNA target sites
TMC7	miRNA target sites
TP53	miRNA target sites
ADAM9	miRNA target sites
VOPP1	miRNA target sites
KIF21B	miRNA target sites

Extended variants
information (count: 10754 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:10754 , 50 per page) page: 1 2 3 4 5 6 7 ... 216

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539937046	chr11:67510614-67510615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572954922	chr11:67510623-67510624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192819912	chr11:67510624-67510625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540435837	chr11:67510628-67510629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568823101	chr11:67510631-67510632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12270076	chr11:67510642-67510643	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184943177	chr11:67510647-67510648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189455136	chr11:67510681-67510682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113702300	chr11:67510685-67510686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563172211	chr11:67510686-67510687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12283217	chr11:67510688-67510689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35887162	chr11:67510691-67510692	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs528157049	chr11:67510702-67510703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10791931	chr11:67510708-67510709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs112892040	chr11:67510729-67510730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540398254	chr11:67510741-67510742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368264890	chr11:67510746-67510747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538598962	chr11:67510768-67510769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183734816	chr11:67510807-67510808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555918186	chr11:67510861-67510862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12278531	chr11:67510990-67510991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544828223	chr11:67510997-67510998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188106001	chr11:67511032-67511033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566659013	chr11:67511041-67511042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534008010	chr11:67511042-67511043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558772695	chr11:67511043-67511044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12284769	chr11:67511144-67511145	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182022680	chr11:67511170-67511171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569935195	chr11:67511177-67511178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111960696	chr11:67511210-67511211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545775371	chr11:67511212-67511213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556817641	chr11:67511248-67511249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143655179	chr11:67511249-67511250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12271586	chr11:67511252-67511253	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs111255137	chr11:67511253-67511254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143122098	chr11:67511260-67511261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528245112	chr11:67511266-67511267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148279339	chr11:67511274-67511275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113604259	chr11:67511278-67511279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564789050	chr11:67511286-67511287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532339431	chr11:67511287-67511288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186066876	chr11:67511297-67511298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569150007	chr11:67511366-67511367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141301008	chr11:67511367-67511368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370016403	chr11:67511391-67511392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150721764	chr11:67511392-67511393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566524978	chr11:67511397-67511398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114028809	chr11:67511447-67511448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559018475	chr11:67511513-67511514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs137953232	chr11:67511564-67511565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1475 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67499800-67512800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:67499800-67515200	Weak transcription	Right Atrium	heart
3	chr11:67500000-67521400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr11:67506000-67512600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:67506400-67511600	Weak transcription	Placenta	Placenta
6	chr11:67511000-67513000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:67511200-67512200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:67511200-67513000	Enhancers	Fetal Heart	heart
9	chr11:67511400-67512000	Enhancers	Fetal Muscle Trunk	muscle
10	chr11:67511600-67511800	Enhancers	Left Ventricle	heart
11	chr11:67511600-67512000	Enhancers	Fetal Muscle Leg	muscle
12	chr11:67511600-67512200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:67511600-67512400	Enhancers	Placenta	Placenta
14	chr11:67512000-67512600	Weak transcription	Gastric	stomach
15	chr11:67512400-67512600	Active TSS	Fetal Lung	lung
16	chr11:67512400-67521000	Weak transcription	Placenta	Placenta
17	chr11:67512600-67512800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:67512600-67512800	Enhancers	Left Ventricle	heart
19	chr11:67512600-67513000	Flanking Active TSS	Fetal Lung	lung
20	chr11:67512600-67513000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
21	chr11:67512600-67513200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:67512600-67513200	Enhancers	Esophagus	oesophagus
23	chr11:67512600-67513200	ZNF genes & repeats	Fetal Kidney	kidney
24	chr11:67512600-67513200	ZNF genes & repeats	Gastric	stomach
25	chr11:67512600-67513200	Active TSS	Pancreas	Pancrea
26	chr11:67512600-67513200	Enhancers	Spleen	Spleen
27	chr11:67512800-67513000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:67512800-67513200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr11:67512800-67513200	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:67512800-67513200	Bivalent/Poised TSS	NHDF-Ad	bronchial
31	chr11:67513000-67513200	Active TSS	Fetal Lung	lung
32	chr11:67513000-67515600	Weak transcription	Fetal Heart	heart
33	chr11:67513000-67519000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr11:67513200-67514000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr11:67513200-67521400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr11:67513200-67525400	Weak transcription	Fetal Kidney	kidney
37	chr11:67514400-67515400	Enhancers	Primary B cells from peripheral blood	blood
38	chr11:67514600-67515000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:67514800-67515200	Enhancers	Fetal Stomach	stomach
40	chr11:67515200-67515400	Weak transcription	Fetal Stomach	stomach
41	chr11:67515400-67515800	Enhancers	Fetal Stomach	stomach
42	chr11:67515600-67516200	Enhancers	Fetal Heart	heart
43	chr11:67515600-67516600	Enhancers	Colon Smooth Muscle	Colon
44	chr11:67515800-67521200	Weak transcription	Fetal Stomach	stomach
45	chr11:67516200-67521200	Weak transcription	Fetal Heart	heart
46	chr11:67517600-67524400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr11:67521000-67521200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:67521000-67521200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr11:67521000-67521600	Enhancers	Fetal Muscle Leg	muscle
50	chr11:67521000-67521600	Enhancers	Ovary	ovary

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