Variant report

Variant	esv1810710
Chromosome Location	chr11:67437879-67442661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:75)
CpG islands
(count:366)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:75 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr11:67440224-67440380	K562	blood:	n/a	n/a
2	CEBPB	chr11:67442059-67442230	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr11:67441909-67442438	ECC-1	luminal epithelium:	n/a	n/a
4	CEBPB	chr11:67441860-67442529	MCF-7	breast:	n/a	n/a
5	CEBPB	chr11:67441830-67442484	MCF-7	breast:	n/a	n/a
6	CHD2	chr11:67442173-67442373	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr11:67437936-67437982	Spleen_OC	spleen:	n/a	n/a
8	ELF1	chr11:67441908-67442731	MCF-7	breast:	n/a	n/a
9	ELF1	chr11:67441797-67442661	MCF-7	breast:	n/a	n/a
10	EP300	chr11:67441906-67442532	T-47D	breast:	n/a	n/a
11	EP300	chr11:67441896-67442540	MCF-7	breast:	n/a	n/a
12	EP300	chr11:67441996-67442591	ECC-1	luminal epithelium:	n/a	n/a
13	EP300	chr11:67441915-67442421	T-47D	breast:	n/a	n/a
14	EP300	chr11:67441893-67442622	MCF-7	breast:	n/a	n/a
15	EP300	chr11:67441998-67442509	ECC-1	luminal epithelium:	n/a	n/a
16	ESR1	chr11:67442013-67442466	T-47D	breast:	n/a	n/a
17	FOS	chr11:67441985-67442216	MCF10A-Er-Src	breast:	n/a	n/a
18	FOXA1	chr11:67442027-67442454	T-47D	breast:	n/a	n/a
19	FOXA1	chr11:67441971-67442394	T-47D	breast:	n/a	n/a
20	GABPA	chr11:67441917-67442505	MCF-7	breast:	n/a	n/a
21	GATA3	chr11:67441880-67442881	MCF-7	breast:	n/a	n/a
22	GATA3	chr11:67441868-67442613	MCF-7	breast:	n/a	n/a
23	GATA3	chr11:67441946-67442515	T-47D	breast:	n/a	n/a
24	GATA3	chr11:67441971-67442538	T-47D	breast:	n/a	n/a
25	GATA3	chr11:67442032-67442521	MCF-7	breast:	n/a	n/a
26	HDAC2	chr11:67441951-67442567	MCF-7	breast:	n/a	n/a
27	HDAC2	chr11:67441771-67442721	MCF-7	breast:	n/a	chr11:67442605-67442624
28	IRF4	chr11:67437040-67437912	GM12878	blood:	n/a	n/a
29	IRF4	chr11:67437083-67437950	GM12878	blood:	n/a	n/a
30	JUND	chr11:67442131-67442241	H1-hESC	embryonic stem cell:	n/a	n/a
31	MAX	chr11:67442017-67442478	ECC-1	luminal epithelium:	n/a	chr11:67442124-67442133
32	MAX	chr11:67442006-67442526	ECC-1	luminal epithelium:	n/a	chr11:67442124-67442133
33	MAX	chr11:67441849-67442530	MCF-7	breast:	n/a	chr11:67442124-67442133
34	MAX	chr11:67441766-67442646	MCF-7	breast:	n/a	chr11:67442124-67442133
35	MYC	chr11:67441985-67442367	MCF-7	breast:	n/a	chr11:67442124-67442133
36	MYC	chr11:67442070-67442279	MCF-7	breast:	n/a	chr11:67442124-67442133
37	MYC	chr11:67441877-67442333	MCF10A-Er-Src	breast:	n/a	chr11:67442124-67442133
38	MYC	chr11:67442192-67442223	MCF-7	breast:	n/a	n/a
39	NFIC	chr11:67441913-67442579	ECC-1	luminal epithelium:	n/a	n/a
40	NFIC	chr11:67441895-67442592	ECC-1	luminal epithelium:	n/a	n/a
41	NR2F2	chr11:67441821-67442640	MCF-7	breast:	n/a	n/a
42	NR2F2	chr11:67442018-67442630	MCF-7	breast:	n/a	n/a
43	NR3C1	chr11:67442061-67442346	ECC-1	luminal epithelium:	n/a	n/a
44	PML	chr11:67441894-67442504	MCF-7	breast:	n/a	n/a
45	POLR2A	chr11:67437864-67438099	MCF-7	breast:	n/a	n/a
46	POLR2A	chr11:67441883-67442376	MCF-7	breast:	n/a	n/a
47	POLR2A	chr11:67441858-67442281	MCF-7	breast:	n/a	n/a
48	POLR2A	chr11:67438173-67438178	MCF-7	breast:	n/a	n/a
49	POLR2A	chr11:67441914-67442205	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr11:67437855-67437882	MCF-7	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67442126-67442176	NHDF-neo	bronchial:	n/a
2	chr11:67442075-67442125	ECC-1	luminal epithelium:	n/a
3	chr11:67442067-67442117	Caco-2	colon:	n/a
4	chr11:67442249-67442299	CMK	blood:	n/a
5	chr11:67442249-67442299	HNPCEpiC	eye:	n/a
6	chr11:67442126-67442176	T-47D	breast:	n/a
7	chr11:67442067-67442117	HRCEpiC	kidney:	n/a
8	chr11:67442249-67442299	NH-A	brain:	n/a
9	chr11:67442408-67442458	GM12892	blood:	n/a
10	chr11:67442195-67442245	NH-A	brain:	n/a
11	chr11:67442195-67442245	NB4	blood:	n/a
12	chr11:67442408-67442458	BJ	skin:	n/a
13	chr11:67442067-67442117	HCM	heart:	n/a
14	chr11:67442067-67442117	GM12878	blood:	n/a
15	chr11:67442126-67442176	HCF	heart:	n/a
16	chr11:67442075-67442125	HAEpiC	amniotic membrane:	n/a
17	chr11:67442249-67442299	AG09319	gingival:	n/a
18	chr11:67442126-67442176	HCT-116	colon:	n/a
19	chr11:67442126-67442176	Hela-S3	cervix:	n/a
20	chr11:67442075-67442125	ovcar-3	ovarian:	n/a
21	chr11:67442126-67442176	Jurkat	blood:	n/a
22	chr11:67442126-67442176	SK-N-MC	brain:	n/a
23	chr11:67442075-67442125	IMR90	lung:	fetal
24	chr11:67442075-67442125	Hepatocyte	liver:	n/a
25	chr11:67442195-67442245	HCF	heart:	n/a
26	chr11:67442067-67442117	H1-hESC	embryonic stem cell:	embryo
27	chr11:67442195-67442245	NT2-D1	testis:	n/a
28	chr11:67442249-67442299	HepG2	liver:	n/a
29	chr11:67442408-67442458	Hepatocyte	liver:	n/a
30	chr11:67442408-67442458	MCF-7	breast:	n/a
31	chr11:67442249-67442299	Jurkat	blood:	n/a
32	chr11:67442126-67442176	ECC-1	luminal epithelium:	n/a
33	chr11:67442075-67442125	Caco-2	colon:	n/a
34	chr11:67442408-67442458	HCF	heart:	n/a
35	chr11:67442195-67442245	HEEpiC	esophagus:	n/a
36	chr11:67442195-67442245	HPAEpiC	pulmonary alveolar:	n/a
37	chr11:67442126-67442176	IMR90	lung:	fetal
38	chr11:67442075-67442125	U87	brain:	n/a
39	chr11:67442249-67442299	HPAEpiC	pulmonary alveolar:	n/a
40	chr11:67442126-67442176	ProgFib	skin:	n/a
41	chr11:67442126-67442176	HRE	kidney:	n/a
42	chr11:67442249-67442299	HCT-116	colon:	n/a
43	chr11:67442408-67442458	GM12878	blood:	n/a
44	chr11:67442067-67442117	CMK	blood:	n/a
45	chr11:67442408-67442458	SKMC	muscle:	n/a
46	chr11:67442408-67442458	SK-N-SH_RA	brain:	n/a
47	chr11:67442126-67442176	PANC-1	pancreas:	n/a
48	chr11:67442067-67442117	AG04449	skin:	fetal
49	chr11:67442249-67442299	HRE	kidney:	n/a
50	chr11:67442408-67442458	HEEpiC	esophagus:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67434481..67439568-chr11:67439660..67443258,9	MCF-7	breast:
2	chr11:67437911..67440480-chr11:67441652..67443889,5	MCF-7	breast:
3	chr11:67396980..67398688-chr11:67437438..67439851,2	MCF-7	breast:
4	chr11:67397077..67399431-chr11:67436542..67439337,2	K562	blood:
5	chr11:67437911..67440480-chr11:67441652..67443889,5	MCF-7	breast:
6	chr11:67397074..67400069-chr11:67440700..67443508,3	K562	blood:
7	chr11:67438405..67443993-chr11:67447780..67452157,7	MCF-7	breast:
8	chr11:67397074..67400069-chr11:67440700..67443508,2	K562	blood:
9	chr11:67434481..67439568-chr11:67439660..67443258,9	MCF-7	breast:
10	chr11:67433386..67435111-chr11:67439487..67442786,3	MCF-7	breast:

No data

Variant related genes	Relation type
ALDH3B2	TF binding region
ALDH3B2	CpG island
ENSG00000132746	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000239559	chromatin interactions

Extended variants
information (count: 232 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:232 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1871031	chr11:67437879-67437880	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550884241	chr11:67437921-67437922	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs374148216	chr11:67437928-67437929	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs569236821	chr11:67437936-67437937	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs536937693	chr11:67437946-67437947	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs555110841	chr11:67437972-67437973	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs192074388	chr11:67437982-67437983	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs534424242	chr11:67438006-67438007	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs151284528	chr11:67438072-67438073	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78149231	chr11:67438122-67438123	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs76053964	chr11:67438137-67438138	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs185035403	chr11:67438142-67438143	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs370727740	chr11:67438175-67438176	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs374056763	chr11:67438178-67438179	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs187809797	chr11:67438194-67438195	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs4313593	chr11:67438195-67438196	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs528445012	chr11:67438215-67438216	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs546793986	chr11:67438234-67438235	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs375933532	chr11:67438235-67438236	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs142770127	chr11:67438236-67438237	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs550796375	chr11:67438246-67438247	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs140489999	chr11:67438276-67438277	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs536591041	chr11:67438279-67438280	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs561198159	chr11:67438281-67438282	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs4569014	chr11:67438284-67438285	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs75775575	chr11:67438325-67438326	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534578756	chr11:67438385-67438386	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs376653631	chr11:67438388-67438389	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs368432034	chr11:67438398-67438399	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs116267644	chr11:67438399-67438400	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs538725713	chr11:67438403-67438404	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs184195662	chr11:67438443-67438444	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs5019163	chr11:67438476-67438477	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs115626499	chr11:67438480-67438481	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs5019164	chr11:67438492-67438493	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs573178416	chr11:67438501-67438502	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs61894527	chr11:67438513-67438514	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs61894528	chr11:67438563-67438564	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111820481	chr11:67438577-67438578	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs555105981	chr11:67438578-67438579	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs373521814	chr11:67438608-67438609	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs114775458	chr11:67438611-67438612	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs115717418	chr11:67438650-67438651	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs76415628	chr11:67438666-67438667	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs530275900	chr11:67438672-67438673	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs375774001	chr11:67438755-67438756	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs548618985	chr11:67438775-67438776	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs144808198	chr11:67438790-67438791	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs138647514	chr11:67438832-67438833	Weak transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs546656569	chr11:67438837-67438838	Weak transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Lung cancer	19153074	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
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67430600-67440800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:67434000-67442400	Weak transcription	Fetal Intestine Small	intestine
3	chr11:67434400-67438600	Enhancers	Placenta	Placenta
4	chr11:67435600-67438200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr11:67435600-67438400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:67437000-67438400	Weak transcription	Primary B cells from cord blood	blood
7	chr11:67437200-67441600	Weak transcription	Gastric	stomach
8	chr11:67437800-67438000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:67437800-67438000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr11:67437800-67438000	Enhancers	Fetal Thymus	thymus
11	chr11:67437800-67438000	Flanking Active TSS	Dnd41	blood
12	chr11:67437800-67438400	Enhancers	Thymus	Thymus
13	chr11:67437800-67439000	Genic enhancers	Esophagus	oesophagus
14	chr11:67438000-67438400	Weak transcription	Fetal Thymus	thymus
15	chr11:67438000-67438600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:67438000-67439000	Enhancers	Dnd41	blood
17	chr11:67438000-67442000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr11:67438200-67438600	Enhancers	Primary hematopoietic stem cells	blood
19	chr11:67438400-67438800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:67438400-67438800	Enhancers	Primary B cells from cord blood	blood
21	chr11:67438400-67439000	Enhancers	Fetal Thymus	thymus
22	chr11:67438600-67439000	Flanking Active TSS	Placenta	Placenta
23	chr11:67438600-67441000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:67438800-67440800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:67439000-67440800	Weak transcription	Esophagus	oesophagus
26	chr11:67439000-67441000	Enhancers	Placenta	Placenta
27	chr11:67439000-67442000	Weak transcription	Dnd41	blood
28	chr11:67440800-67441000	Flanking Active TSS	Esophagus	oesophagus
29	chr11:67440800-67441800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:67440800-67443200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr11:67441000-67441200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr11:67441000-67441200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:67441000-67441200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
34	chr11:67441000-67441400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr11:67441000-67442200	Active TSS	Esophagus	oesophagus
36	chr11:67441000-67442200	Flanking Active TSS	Placenta	Placenta
37	chr11:67441200-67441400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr11:67441200-67442200	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr11:67441200-67443200	Enhancers	Placenta Amnion	Placenta Amnion
40	chr11:67441200-67443400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:67441400-67442200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:67441400-67442600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr11:67441400-67443000	Enhancers	NHEK	skin
44	chr11:67441400-67443400	Enhancers	Stomach Mucosa	stomach
45	chr11:67441600-67441800	Enhancers	Fetal Brain Male	brain
46	chr11:67441600-67443200	Enhancers	Gastric	stomach
47	chr11:67441600-67443200	Enhancers	Pancreas	Pancrea
48	chr11:67441600-67443200	Enhancers	HMEC	breast
49	chr11:67441800-67442200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:67441800-67442800	Enhancers	Colonic Mucosa	Colon

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