Variant report

Variant	esv3444139
Chromosome Location	chr6:58777810-58779696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:105)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:57697051..57699517-chr6:58775454..58778452,2	MCF-7	breast:
2	chr3:90450069..90451571-chr6:58776178..58778913,3	MCF-7	breast:
3	chr6:58777333..58777900-chr8:122346827..122347447,2	MCF-7	breast:
4	chr6:49499719..49500373-chr6:58777827..58778441,2	MCF-7	breast:
5	chr20:46129644..46132043-chr6:58777544..58779139,2	MCF-7	breast:
6	chr17:57920709..57924714-chr6:58775095..58779071,5	MCF-7	breast:
7	chr6:58776120..58778273-chr8:145699925..145701982,2	MCF-7	breast:
8	chr4:44422694..44424195-chr6:58776128..58778515,2	MCF-7	breast:
9	chr6:58776666..58779159-chr8:125462787..125464378,2	MCF-7	breast:
10	chr18:55334307..55335255-chr6:58777372..58777917,2	MCF-7	breast:
11	chr6:58777220..58778210-chr6:119855510..119856349,2	MCF-7	breast:
12	chr17:59487756..59489295-chr6:58776969..58779008,2	MCF-7	breast:
13	chr20:62493089..62495109-chr6:58777340..58778920,2	MCF-7	breast:
14	chr6:27805995..27806602-chr6:58778107..58778767,2	MCF-7	breast:
15	chr6:58777671..58778345-chr6:61909292..61909815,4	MCF-7	breast:
16	chr2:219259923..219262856-chr6:58776591..58778942,2	MCF-7	breast:
17	chr17:46984708..46987154-chr6:58777011..58778755,2	MCF-7	breast:
18	chr1:110090644..110091238-chr6:58776881..58777871,2	MCF-7	breast:
19	chr6:58777416..58779792-chr6:77801547..77804072,2	MCF-7	breast:
20	chr1:144533667..144534206-chr6:58778266..58778827,2	Hela-S3	cervix:
21	chr6:58777712..58778738-chr6:61909295..61909815,6	MCF-7	breast:
22	chr3:63980131..63982580-chr6:58776275..58779243,2	MCF-7	breast:
23	chr17:57928094..57930742-chr6:58776120..58778676,4	MCF-7	breast:
24	chr2:135217803..135218666-chr6:58777553..58778353,2	MCF-7	breast:
25	chr14:70592691..70594528-chr6:58777109..58778754,2	MCF-7	breast:
26	chr20:60960325..60962671-chr6:58777619..58780127,2	MCF-7	breast:
27	chr6:58777390..58779179-chr6:133135024..133136911,2	MCF-7	breast:
28	chr6:31849956..31851616-chr6:58776203..58778751,2	MCF-7	breast:
29	chr2:38304500..38306516-chr6:58776846..58778352,2	MCF-7	breast:
30	chr6:58776797..58778439-chr9:136323811..136326318,2	MCF-7	breast:
31	chr20:17516282..17517977-chr6:58775914..58778767,2	MCF-7	breast:
32	chr17:56707689..56709464-chr6:58776179..58779153,2	MCF-7	breast:
33	chr15:91473255..91473790-chr6:58778382..58779186,2	MCF-7	breast:
34	chr6:58777651..58778267-chr6:61909313..61909813,3	MCF-7	breast:
35	chr13:20943879..20946266-chr6:58777671..58779217,2	MCF-7	breast:
36	chr11:75291642..75294590-chr6:58777397..58779135,2	MCF-7	breast:
37	chr1:9910788..9913768-chr6:58778329..58780695,2	MCF-7	breast:
38	chr16:73430630..73432387-chr6:58777761..58779339,2	MCF-7	breast:
39	chr1:121484489..121485231-chr6:58779321..58780005,2	MCF-7	breast:
40	chr18:73688396..73689210-chr6:58777841..58778684,2	MCF-7	breast:
41	chr6:58778243..58779030-chrX:61731310..61731811,2	MCF-7	breast:
42	chr3:90451069..90451589-chr6:58776919..58777844,3	MCF-7	breast:
43	chr17:66287677..66288456-chr6:58778380..58779126,2	MCF-7	breast:
44	chr16:85495639..85498852-chr6:58775657..58778770,3	MCF-7	breast:
45	chr3:16360548..16361058-chr6:58778316..58779058,2	MCF-7	breast:
46	chr17:62622662..62623234-chr6:58778443..58779436,2	MCF-7	breast:
47	chr6:58778318..58779144-chr9:130843661..130844171,2	MCF-7	breast:
48	chr6:58776953..58777924-chr9:126446426..126447140,2	MCF-7	breast:
49	chr17:56736044..56736561-chr6:58778407..58779097,2	MCF-7	breast:
50	chr17:57914586..57918340-chr6:58776843..58780440,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000199004	chromatin interactions
ENSG00000268858	chromatin interactions
ENSG00000103528	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000237080	chromatin interactions
ENSG00000026103	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000089351	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000257084	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000226137	chromatin interactions
ENSG00000140553	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000212017	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000255326	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000175866	chromatin interactions
ENSG00000230513	chromatin interactions
ENSG00000104524	chromatin interactions
ENSG00000141367	chromatin interactions
ENSG00000160973	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000160325	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000204272	chromatin interactions
ENSG00000207713	chromatin interactions
ENSG00000183665	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000185158	chromatin interactions
ENSG00000206754	chromatin interactions
ENSG00000126749	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000159202	chromatin interactions
ENSG00000184436	chromatin interactions
ENSG00000048392	chromatin interactions
ENSG00000248278	chromatin interactions
ENSG00000065135	chromatin interactions
ENSG00000171858	chromatin interactions
ENSG00000132470	chromatin interactions
ENSG00000111321	chromatin interactions
ENSG00000207708	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000163635	chromatin interactions

Extended variants
information (count: 1026 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28816532	chr6:58777811-58777812	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
2	rs9500188	chr6:58777812-58777813	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
3	rs4928615	chr6:58777813-58777814	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
4	rs4598114	chr6:58777814-58777815	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
5	rs4928380	chr6:58777815-58777816	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
6	rs9404680	chr6:58777816-58777817	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
7	rs28837863	chr6:58777818-58777819	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
8	rs12203463	chr6:58777819-58777820	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
9	rs58696588	chr6:58777820-58777821	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
10	rs9500551	chr6:58777822-58777823	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
11	rs4928617	chr6:58777825-58777826	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
12	rs28843742	chr6:58777826-58777827	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
13	rs4374849	chr6:58777827-58777828	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
14	rs11211786	chr6:58777828-58777829	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
15	rs9391344	chr6:58777829-58777830	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
16	rs4928382	chr6:58777830-58777831	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
17	rs28787570	chr6:58777831-58777832	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
18	rs9500552	chr6:58777832-58777833	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
19	rs9500553	chr6:58777835-58777836	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
20	rs9632517	chr6:58777836-58777837	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
21	rs4374850	chr6:58777837-58777838	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
22	rs9500554	chr6:58777839-58777840	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
23	rs9500555	chr6:58777842-58777843	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
24	rs55768201	chr6:58777844-58777845	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
25	rs9391492	chr6:58777845-58777846	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
26	rs55844021	chr6:58777846-58777847	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
27	rs4273718	chr6:58777847-58777848	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
28	rs9500556	chr6:58777849-58777850	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
29	rs28883420	chr6:58777850-58777851	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
30	rs4642506	chr6:58777851-58777852	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
31	rs58113837	chr6:58777852-58777853	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
32	rs4292553	chr6:58777854-58777855	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
33	rs9500557	chr6:58777855-58777856	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
34	rs9391346	chr6:58777856-58777857	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
35	rs4928618	chr6:58777857-58777858	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
36	rs9500558	chr6:58777858-58777859	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
37	rs4389790	chr6:58777859-58777860	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
38	rs71212180	chr6:58777861-58777862	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
39	rs4644092	chr6:58777863-58777864	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	45 gene(s)	Overlapped CNVs	n/a
40	rs28884537	chr6:58777865-58777866	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a
41	rs28776326	chr6:58777866-58777867	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a
42	rs9500559	chr6:58777867-58777868	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a
43	rs9404857	chr6:58777868-58777869	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a
44	rs9404682	chr6:58777869-58777870	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a
45	rs536399260	chr6:58777870-58777871	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a
46	rs9377779	chr6:58777871-58777872	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a
47	rs9391493	chr6:58777874-58777875	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	43 gene(s)	Overlapped CNVs	n/a
48	rs9500560	chr6:58777876-58777877	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	43 gene(s)	Overlapped CNVs	n/a
49	rs28864713	chr6:58777879-58777880	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	43 gene(s)	Overlapped CNVs	n/a
50	rs28818510	chr6:58777880-58777881	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	43 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58773400-58779400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
2	chr6:58773400-58779400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:58773400-58779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:58773400-58779400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
5	chr6:58773400-58779400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr6:58773400-58779400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
7	chr6:58773400-58779400	ZNF genes & repeats	Adipose Nuclei	Adipose
8	chr6:58773400-58779400	ZNF genes & repeats	Fetal Stomach	stomach
9	chr6:58773400-58779400	ZNF genes & repeats	Left Ventricle	heart
10	chr6:58773600-58779200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
11	chr6:58773600-58779400	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
12	chr6:58773600-58779400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr6:58773600-58779400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
14	chr6:58773600-58779400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr6:58773600-58779400	ZNF genes & repeats	Primary B cells from cord blood	blood
16	chr6:58773600-58779400	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
17	chr6:58773600-58779400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:58773600-58779400	ZNF genes & repeats	Fetal Intestine Large	intestine
19	chr6:58776200-58779400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr6:58776400-58778200	ZNF genes & repeats	Brain Germinal Matrix	brain
21	chr6:58776400-58779200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:58776400-58779400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:58776400-58779400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
24	chr6:58776400-58779400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:58776400-58779400	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
26	chr6:58776400-58779400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
27	chr6:58776600-58778000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:58776600-58778000	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
29	chr6:58776600-58778400	ZNF genes & repeats	Esophagus	oesophagus
30	chr6:58776600-58778800	Bivalent/Poised TSS	K562	blood
31	chr6:58776600-58779200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:58776600-58779200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
33	chr6:58776600-58779200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:58776600-58779200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr6:58776600-58779200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:58776600-58779200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr6:58776600-58779200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:58776600-58779200	ZNF genes & repeats	Fetal Brain Male	brain
39	chr6:58776600-58779200	ZNF genes & repeats	Fetal Brain Female	brain
40	chr6:58776600-58779200	ZNF genes & repeats	Fetal Heart	heart
41	chr6:58776600-58779200	ZNF genes & repeats	Fetal Muscle Trunk	muscle
42	chr6:58776600-58779200	ZNF genes & repeats	Lung	lung
43	chr6:58776600-58779200	Flanking Bivalent TSS/Enh	Placenta Amnion	Placenta Amnion
44	chr6:58776600-58779200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
45	chr6:58776600-58779200	Flanking Bivalent TSS/Enh	A549	lung
46	chr6:58776600-58779200	ZNF genes & repeats	GM12878-XiMat	blood
47	chr6:58776600-58779200	ZNF genes & repeats	HMEC	breast
48	chr6:58776600-58779200	Transcr. at gene 5' and 3'	NHEK	skin
49	chr6:58776600-58779400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
50	chr6:58776600-58779400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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