Variant report

Variant	nsv7669
Chromosome Location	chr11:9290376-9335028
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:122)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:9298231-9298413	K562	blood:	n/a	n/a
2	ARID3A	chr11:9324133-9324152	K562	blood:	n/a	n/a
3	ATF2	chr11:9302145-9302607	GM12878	blood:	n/a	n/a
4	BCL3	chr11:9295754-9295978	GM12878	blood:	n/a	n/a
5	CEBPB	chr11:9295220-9295563	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr11:9295248-9295558	IMR90	lung:	n/a	n/a
7	CEBPB	chr11:9298318-9298447	K562	blood:	n/a	n/a
8	CEBPB	chr11:9329283-9329487	K562	blood:	n/a	n/a
9	CEBPB	chr11:9329309-9329455	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:9295246-9295485	K562	blood:	n/a	n/a
11	CEBPB	chr11:9295413-9295421	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr11:9314152-9314192	A549	lung:	n/a	n/a
13	CEBPB	chr11:9334291-9334565	K562	blood:	n/a	n/a
14	CEBPB	chr11:9295273-9295511	K562	blood:	n/a	n/a
15	CTCF	chr11:9298318-9298410	MCF-7	breast:	n/a	n/a
16	CTCF	chr11:9298020-9298545	HCT-116	colon:	n/a	n/a
17	CTCF	chr11:9298178-9298459	A549	lung:	n/a	n/a
18	CTCF	chr11:9309760-9309888	K562	blood:	n/a	chr11:9309836-9309857
19	CTCF	chr11:9309823-9309918	GM12878	blood:	n/a	chr11:9309836-9309857
20	CTCF	chr11:9298260-9298410	Caco-2	colon:	n/a	n/a
21	CTCF	chr11:9298233-9298433	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:9298200-9298350	HEK293	kidney:	n/a	n/a
23	CTCF	chr11:9298119-9298623	A549	lung:	n/a	n/a
24	CTCF	chr11:9309817-9309901	Medullo	brain:	n/a	chr11:9309836-9309857
25	CTCF	chr11:9312835-9312861	Fibrobl	skin:	n/a	n/a
26	CTCF	chr11:9298311-9298413	A549	lung:	n/a	n/a
27	CTCF	chr11:9298212-9298527	K562	blood:	n/a	n/a
28	CTCF	chr11:9298259-9298409	K562	blood:	n/a	n/a
29	CTCF	chr11:9298169-9298484	GM12878	blood:	n/a	n/a
30	CTCF	chr11:9298311-9298395	Gliobla	brain:	n/a	n/a
31	CTCF	chr11:9298189-9298417	A549	lung:	n/a	n/a
32	CTCF	chr11:9309793-9309938	HUVEC	blood vessel:	n/a	chr11:9309836-9309857
33	CTCF	chr11:9317140-9317164	ProgFib	skin:	n/a	n/a
34	CTCF	chr11:9298255-9298418	HepG2	liver:	n/a	n/a
35	CTCF	chr11:9311583-9311618	GM13977	blood:	n/a	n/a
36	CTCF	chr11:9294980-9295130	GM12869	blood:	n/a	n/a
37	CTCF	chr11:9298123-9298509	A549	lung:	n/a	n/a
38	CTCF	chr11:9298294-9298410	GM12892	blood:	n/a	n/a
39	CTCF	chr11:9294668-9294739	GM10266	blood:	n/a	n/a
40	CTCF	chr11:9298240-9298390	A549	lung:	n/a	n/a
41	CTCF	chr11:9309839-9309917	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr11:9298300-9298450	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr11:9298300-9298450	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr11:9309778-9309942	Hela-S3	cervix:	n/a	chr11:9309836-9309857
45	CTCF	chr11:9325320-9325470	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr11:9298339-9298408	GM19239	blood:	n/a	n/a
47	CTCF	chr11:9298343-9298426	MCF-7	breast:	n/a	n/a
48	CTCF	chr11:9298309-9298443	MCF-7	breast:	n/a	n/a
49	CTCF	chr11:9298279-9298374	Medullo	brain:	n/a	n/a
50	CTCF	chr11:9298237-9298432	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9304142-9304192	HCT-116	colon:	n/a
2	chr11:9304142-9304192	MCF-7	breast:	n/a
3	chr11:9333358-9333408	HUVEC	blood vessel:	n/a
4	chr11:9333358-9333408	BJ	skin:	n/a
5	chr11:9333358-9333408	GM12892	blood:	n/a
6	chr11:9304142-9304192	ECC-1	luminal epithelium:	n/a
7	chr11:9304142-9304192	BE2_C	brain:	n/a
8	chr11:9304142-9304192	HAEpiC	amniotic membrane:	n/a
9	chr11:9333358-9333408	IMR90	lung:	fetal
10	chr11:9304142-9304192	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:9304142-9304192	PANC-1	pancreas:	n/a
12	chr11:9333358-9333408	PFSK-1	brain:	n/a
13	chr11:9333358-9333408	ProgFib	skin:	n/a
14	chr11:9304142-9304192	LNCaP	prostate:	n/a
15	chr11:9333358-9333408	HRE	kidney:	n/a
16	chr11:9333358-9333408	GM06990	blood:	n/a
17	chr11:9333358-9333408	GM19239	blood:	n/a
18	chr11:9304142-9304192	HNPCEpiC	eye:	n/a
19	chr11:9304142-9304192	CMK	blood:	n/a
20	chr11:9333358-9333408	T-47D	breast:	n/a
21	chr11:9304142-9304192	U87	brain:	n/a
22	chr11:9304142-9304192	PrEC	prostate:	n/a
23	chr11:9304142-9304192	AoSMC	blood vessel:	n/a
24	chr11:9333358-9333408	HAEpiC	amniotic membrane:	n/a
25	chr11:9333358-9333408	ovcar-3	ovarian:	n/a
26	chr11:9333358-9333408	A549	lung:	n/a
27	chr11:9333358-9333408	HMEC	breast:	n/a
28	chr11:9333358-9333408	HepG2	liver:	n/a
29	chr11:9304142-9304192	HepG2	liver:	n/a
30	chr11:9333358-9333408	Jurkat	blood:	n/a
31	chr11:9333358-9333408	HCT-116	colon:	n/a
32	chr11:9333358-9333408	MCF-7	breast:	n/a
33	chr11:9333358-9333408	U87	brain:	n/a
34	chr11:9304142-9304192	SKMC	muscle:	n/a
35	chr11:9333358-9333408	Caco-2	colon:	n/a
36	chr11:9333358-9333408	HCM	heart:	n/a
37	chr11:9304142-9304192	AG10803	skin:	n/a
38	chr11:9333358-9333408	AG04450	lung:	fetal
39	chr11:9304142-9304192	AG09319	gingival:	n/a
40	chr11:9304142-9304192	GM12878	blood:	n/a
41	chr11:9333358-9333408	HIPEpiC	eye:	n/a
42	chr11:9304142-9304192	AG04449	skin:	fetal
43	chr11:9304142-9304192	A549	lung:	n/a
44	chr11:9333358-9333408	SK-N-MC	brain:	n/a
45	chr11:9333358-9333408	SK-N-SH	brain:	n/a
46	chr11:9304142-9304192	Jurkat	blood:	n/a
47	chr11:9304142-9304192	NHBE	bronchial:	n/a
48	chr11:9333358-9333408	NHBE	bronchial:	n/a
49	chr11:9333358-9333408	Hela-S3	cervix:	n/a
50	chr11:9304142-9304192	HRPEpiC	eye:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:9286396..9288555-chr11:9303070..9305468,2	K562	blood:
2	chr11:9294384..9296352-chr11:9307669..9309311,2	K562	blood:
3	chr11:9301124..9302676-chr11:9383482..9385931,2	K562	blood:
4	chr11:9320121..9322582-chr11:9335462..9337660,2	K562	blood:
5	chr11:9278298..9280527-chr11:9313092..9315469,2	K562	blood:
6	chr11:9328481..9330937-chr11:9481410..9482943,2	MCF-7	breast:
7	chr11:9285320..9287424-chr11:9318280..9320535,2	K562	blood:
8	chr11:9285423..9287912-chr11:9289448..9291487,2	MCF-7	breast:
9	chr11:9315035..9317073-chr11:9404737..9406993,2	K562	blood:
10	chr11:9286168..9287841-chr11:9289987..9292577,2	K562	blood:
11	chr11:9334942..9338160-chr11:9405201..9408296,5	MCF-7	breast:
12	chr11:9283842..9286911-chr11:9307794..9310804,4	K562	blood:
13	chr11:9326826..9328669-chr11:9330694..9332491,2	K562	blood:
14	chr11:9316943..9319199-chr11:9321655..9323938,2	K562	blood:
15	chr11:9316943..9319199-chr11:9321655..9323938,2	K562	blood:
16	chr11:9290328..9292720-chr11:9293368..9296005,3	K562	blood:
17	chr11:9328690..9334073-chr11:9404480..9408917,7	K562	blood:
18	chr11:9316306..9317973-chr11:9319550..9321312,2	K562	blood:
19	chr11:9329616..9332510-chr11:9482010..9484276,2	K562	blood:
20	chr11:9328102..9338305-chr11:9404480..9412498,38	K562	blood:
21	chr11:9334187..9337944-chr11:9481178..9484496,6	K562	blood:
22	chr11:9316306..9317973-chr11:9319550..9321312,2	K562	blood:
23	chr11:9290328..9292720-chr11:9293368..9296005,3	K562	blood:
24	chr11:9321121..9324155-chr11:9406069..9408356,3	K562	blood:
25	chr11:9323308..9325382-chr11:9329913..9332100,2	K562	blood:
26	chr11:9320121..9324688-chr11:9334835..9338165,5	K562	blood:
27	chr11:9287022..9288899-chr11:9296705..9299539,3	MCF-7	breast:
28	chr11:9334169..9339249-chr11:9404487..9409469,24	K562	blood:
29	chr11:9323308..9325382-chr11:9329913..9332100,2	K562	blood:
30	chr11:9282323..9285944-chr11:9290054..9293255,4	K562	blood:
31	chr11:9326826..9328669-chr11:9330694..9332491,2	K562	blood:
32	chr11:9333668..9337804-chr11:9478729..9484496,11	K562	blood:
33	chr11:9324025..9326025-chr11:9386165..9388976,2	K562	blood:
34	chr11:9305631..9308586-chr11:9405162..9407062,2	MCF-7	breast:
35	chr11:9334944..9338278-chr11:9404354..9407861,9	MCF-7	breast:
36	chr11:9283600..9286553-chr11:9290163..9293255,5	K562	blood:
37	chr11:9297957..9298659-chr11:9528266..9529004,3	MCF-7	breast:
38	chr11:9294384..9296715-chr11:9307669..9309886,2	K562	blood:
39	chr11:9333302..9335667-chr11:9353221..9354766,2	K562	blood:
40	chr11:9283945..9288774-chr11:9332278..9339081,12	K562	blood:
41	chr11:8985177..8988020-chr11:9331940..9333549,2	K562	blood:
42	chr11:9294384..9296352-chr11:9307669..9309311,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TMEM41B	hsa-miR-335-5p	chr11:9303207-9303230
2	TMEM41B	hsa-miR-98-5p	chr11:9303459-9303481

Variant related genes	Relation type
ENSG00000254884	TF binding region
DENND5A	TF binding region
TMEM41B	TF binding region
ENSG00000254884	CpG island
DENND5A	CpG island
TMEM41B	CpG island
ENSG00000166471	chromatin interactions
ENSG00000175348	chromatin interactions
ENSG00000254860	chromatin interactions
ENSG00000205339	chromatin interactions
ENSG00000184014	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000268403	chromatin interactions

Extended variants
information (count: 1913 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1913 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35523244	chr11:9290450-9290451	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs566808694	chr11:9290459-9290460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568370950	chr11:9290463-9290464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370647970	chr11:9290505-9290506	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs564466143	chr11:9290514-9290515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533432883	chr11:9290545-9290546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540488367	chr11:9290554-9290555	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560710479	chr11:9290561-9290562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs181679319	chr11:9290562-9290563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs10770002	chr11:9290595-9290596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs11601387	chr11:9290610-9290611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560607346	chr11:9290624-9290625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531786734	chr11:9290647-9290648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142371156	chr11:9290742-9290743	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570773910	chr11:9290771-9290772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539715815	chr11:9290778-9290779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552894567	chr11:9290783-9290784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs539071336	chr11:9290790-9290791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566619412	chr11:9290840-9290841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113524809	chr11:9290850-9290851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs10770003	chr11:9290871-9290872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs184772843	chr11:9290899-9290900	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529284370	chr11:9290902-9290903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557299600	chr11:9290936-9290937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577940906	chr11:9290944-9290945	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141419993	chr11:9290954-9290955	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs371252269	chr11:9290999-9291000	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560531525	chr11:9291068-9291069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11603759	chr11:9291111-9291112	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs369450736	chr11:9291166-9291167	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563000131	chr11:9291167-9291168	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs77983561	chr11:9291191-9291192	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs150366774	chr11:9291239-9291240	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571620734	chr11:9291243-9291244	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs138037567	chr11:9291322-9291323	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs546911944	chr11:9291323-9291324	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs189406586	chr11:9291376-9291377	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs535664838	chr11:9291390-9291391	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs553670513	chr11:9291422-9291423	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs182503352	chr11:9291426-9291427	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537523198	chr11:9291427-9291428	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs367564274	chr11:9291465-9291466	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201961260	chr11:9291466-9291467	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200086468	chr11:9291467-9291468	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs557336362	chr11:9291468-9291469	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577179588	chr11:9291469-9291470	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs200007726	chr11:9291471-9291472	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs201023558	chr11:9291475-9291476	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185912132	chr11:9291534-9291535	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573500748	chr11:9291536-9291537	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1187 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9287400-9291200	Weak transcription	HSMMtube	muscle
2	chr11:9287400-9301600	Weak transcription	Esophagus	oesophagus
3	chr11:9287400-9302000	Weak transcription	Spleen	Spleen
4	chr11:9287400-9319600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr11:9287400-9332600	Weak transcription	HMEC	breast
6	chr11:9287400-9333000	Weak transcription	Gastric	stomach
7	chr11:9287600-9291000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:9287600-9291000	Weak transcription	NHDF-Ad	bronchial
9	chr11:9287600-9291200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr11:9287600-9291200	Weak transcription	NH-A	brain
11	chr11:9287600-9293800	Weak transcription	Left Ventricle	heart
12	chr11:9287600-9295400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr11:9287600-9296200	Weak transcription	Fetal Lung	lung
14	chr11:9287600-9296200	Weak transcription	Right Ventricle	heart
15	chr11:9287600-9299800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:9287600-9301600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:9287600-9301800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr11:9287600-9302000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr11:9287600-9302000	Weak transcription	HSMM	muscle
20	chr11:9287600-9302000	Weak transcription	Osteobl	bone
21	chr11:9287600-9304800	Weak transcription	NHEK	skin
22	chr11:9287600-9319200	Weak transcription	NHLF	lung
23	chr11:9287800-9291000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:9287800-9291000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr11:9287800-9291000	Weak transcription	Right Atrium	heart
26	chr11:9287800-9291000	Weak transcription	Hela-S3	cervix
27	chr11:9287800-9291200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:9287800-9291200	Weak transcription	Fetal Muscle Leg	muscle
29	chr11:9287800-9291200	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr11:9287800-9295800	Weak transcription	Lung	lung
31	chr11:9287800-9296200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr11:9287800-9296400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr11:9287800-9298000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr11:9287800-9298000	Weak transcription	Placenta	Placenta
35	chr11:9287800-9298200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr11:9287800-9298800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:9287800-9300800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:9287800-9301600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:9287800-9301600	Weak transcription	Fetal Intestine Large	intestine
40	chr11:9287800-9301800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr11:9287800-9301800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr11:9287800-9302400	Weak transcription	Brain Germinal Matrix	brain
43	chr11:9287800-9305200	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr11:9287800-9312200	Weak transcription	K562	blood
45	chr11:9287800-9328400	Weak transcription	A549	lung
46	chr11:9287800-9333800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr11:9288000-9296200	Weak transcription	Brain Angular Gyrus	brain
48	chr11:9288000-9301800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:9288000-9320400	Weak transcription	Fetal Kidney	kidney
50	chr11:9288200-9321200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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