Variant report

Variant	nsv553586
Chromosome Location	chr11:17559018-17599093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:587)
CpG islands
(count:1343)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:17572084-17572296	K562	blood:	n/a	n/a
2	BACH1	chr11:17566012-17566149	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr11:17597349-17597729	HepG2	liver:	n/a	chr11:17597468-17597477
4	BHLHE40	chr11:17597341-17597624	K562	blood:	n/a	chr11:17597468-17597477
5	CCNT2	chr11:17593825-17594070	K562	blood:	n/a	n/a
6	CEBPB	chr11:17561324-17561348	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr11:17568597-17569010	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:17588780-17589028	HepG2	liver:	n/a	chr11:17588880-17588889 chr11:17588878-17588889
9	CHD1	chr11:17569793-17569873	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr11:17563107-17563184	HepG2	liver:	n/a	n/a
11	CHD2	chr11:17584988-17585129	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr11:17586320-17586470	GM12865	blood:	n/a	n/a
13	CTCF	chr11:17586270-17586496	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr11:17569620-17569770	NHEK	skin:	n/a	n/a
15	CTCF	chr11:17586360-17586510	HCT-116	colon:	n/a	n/a
16	CTCF	chr11:17586280-17586430	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr11:17586296-17586529	IMR90	lung:	n/a	n/a
18	CTCF	chr11:17570120-17570270	GM12874	blood:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
19	CTCF	chr11:17586268-17586465	HepG2	liver:	n/a	n/a
20	CTCF	chr11:17586280-17586430	GM12878	blood:	n/a	n/a
21	CTCF	chr11:17586115-17586146	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr11:17570100-17570250	NHEK	skin:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
23	CTCF	chr11:17569700-17569850	HRE	kidney:	n/a	n/a
24	CTCF	chr11:17585060-17585210	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr11:17586260-17586410	HL-60	blood:	n/a	n/a
26	CTCF	chr11:17586300-17586450	GM12868	blood:	n/a	n/a
27	CTCF	chr11:17570160-17570310	MCF-7	breast:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
28	CTCF	chr11:17569580-17569830	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr11:17586300-17586450	HepG2	liver:	n/a	n/a
30	CTCF	chr11:17586320-17586470	BE2_C	brain:	n/a	n/a
31	CTCF	chr11:17586340-17586490	GM06990	blood:	n/a	n/a
32	CTCF	chr11:17570187-17570234	GM12878	blood:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
33	CTCF	chr11:17570120-17570270	BE2_C	brain:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
34	CTCF	chr11:17586300-17586450	HMEC	breast:	n/a	n/a
35	CTCF	chr11:17570062-17570251	K562	blood:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
36	CTCF	chr11:17586320-17586470	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr11:17576180-17576330	GM12873	blood:	n/a	n/a
38	CTCF	chr11:17570136-17570285	Kidney_OC	kidney:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
39	CTCF	chr11:17586340-17586490	HCFaa	heart:	n/a	n/a
40	CTCF	chr11:17570100-17570250	HBMEC	blood vessel:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
41	CTCF	chr11:17575580-17575730	GM12868	blood:	n/a	n/a
42	CTCF	chr11:17586260-17586410	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr11:17586360-17586510	RPTEC	kidney:	n/a	n/a
44	CTCF	chr11:17586260-17586410	HVMF	connective:	n/a	n/a
45	CTCF	chr11:17585065-17585186	NHEK	skin:	n/a	n/a
46	CTCF	chr11:17586300-17586450	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr11:17566051-17566163	K562	blood:	n/a	n/a
48	CTCF	chr11:17585080-17585230	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr11:17570080-17570230	HEEpiC	esophagus:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
50	CTCF	chr11:17570135-17570255	MCF-7	breast:	n/a	chr11:17570198-17570208 chr11:17570201-17570210

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17566591-17566641	NHBE	bronchial:	n/a
2	chr11:17566591-17566641	NHBE	bronchial:	n/a
3	chr11:17566591-17566641	AoSMC	blood vessel:	n/a
4	chr11:17566017-17566067	HEK293	kidney:	embryo
5	chr11:17563125-17563175	AG04450	lung:	fetal
6	chr11:17564425-17564475	AG09309	skin:	n/a
7	chr11:17568889-17568939	HEEpiC	esophagus:	n/a
8	chr11:17591837-17591887	NHDF-neo	bronchial:	n/a
9	chr11:17565769-17565819	MCF10A-Er-Src	breast:	n/a
10	chr11:17567447-17567497	Jurkat	blood:	n/a
11	chr11:17566772-17566822	HNPCEpiC	eye:	n/a
12	chr11:17565885-17565935	HMEC	breast:	n/a
13	chr11:17568889-17568939	RPTEC	kidney:	n/a
14	chr11:17566051-17566101	BE2_C	brain:	n/a
15	chr11:17563125-17563175	AG10803	skin:	n/a
16	chr11:17564696-17564746	PrEC	prostate:	n/a
17	chr11:17566591-17566641	K562	blood:	n/a
18	chr11:17567447-17567497	H1-hESC	embryonic stem cell:	embryo
19	chr11:17565885-17565935	HCT-116	colon:	n/a
20	chr11:17563125-17563175	ovcar-3	ovarian:	n/a
21	chr11:17563125-17563175	A549	lung:	n/a
22	chr11:17564425-17564475	AG10803	skin:	n/a
23	chr11:17565878-17565928	HRPEpiC	eye:	n/a
24	chr11:17565878-17565928	SK-N-MC	brain:	n/a
25	chr11:17565744-17565794	HEEpiC	esophagus:	n/a
26	chr11:17591822-17591872	ProgFib	skin:	n/a
27	chr11:17566163-17566213	RPTEC	kidney:	n/a
28	chr11:17566034-17566084	HL-60	blood:	n/a
29	chr11:17566034-17566084	BE2_C	brain:	n/a
30	chr11:17598735-17598785	NB4	blood:	n/a
31	chr11:17565769-17565819	SK-N-MC	brain:	n/a
32	chr11:17566048-17566098	HEK293	kidney:	embryo
33	chr11:17565885-17565935	MCF-7	breast:	n/a
34	chr11:17564425-17564475	HAEpiC	amniotic membrane:	n/a
35	chr11:17565744-17565794	NT2-D1	testis:	n/a
36	chr11:17567447-17567497	AG04449	skin:	fetal
37	chr11:17598735-17598785	GM06990	blood:	n/a
38	chr11:17566048-17566098	GM12878	blood:	n/a
39	chr11:17569556-17569606	Hela-S3	cervix:	n/a
40	chr11:17564696-17564746	HEK293	kidney:	embryo
41	chr11:17564425-17564475	CMK	blood:	n/a
42	chr11:17565744-17565794	PANC-1	pancreas:	n/a
43	chr11:17598735-17598785	PFSK-1	brain:	n/a
44	chr11:17565885-17565935	HEK293	kidney:	embryo
45	chr11:17565878-17565928	T-47D	breast:	n/a
46	chr11:17569556-17569606	U87	brain:	n/a
47	chr11:17566034-17566084	GM06990	blood:	n/a
48	chr11:17566034-17566084	CMK	blood:	n/a
49	chr11:17565878-17565928	Hela-S3	cervix:	n/a
50	chr11:17567447-17567497	HRPEpiC	eye:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17579575..17581891-chr11:17582600..17585148,3	K562	blood:
2	chr11:17567943..17569861-chr11:17577683..17579553,2	K562	blood:
3	chr11:17567135..17572180-chr11:17576316..17581948,6	K562	blood:
4	chr11:17573988..17575798-chr11:17578729..17580759,2	K562	blood:
5	chr11:17567562..17569215-chr11:17583534..17585455,2	K562	blood:
6	chr11:17564338..17566127-chr11:17572702..17576571,3	K562	blood:
7	chr11:17567135..17572180-chr11:17576316..17581948,6	K562	blood:
8	chr11:17520408..17522288-chr11:17583277..17586222,2	K562	blood:
9	chr11:17580038..17581891-chr11:17582778..17585148,2	K562	blood:
10	chr11:17580038..17581891-chr11:17582778..17585148,2	K562	blood:
11	chr11:17557311..17560136-chr11:17561870..17563782,2	K562	blood:
12	chr11:17563988..17566643-chr11:17568666..17571231,2	MCF-7	breast:
13	chr11:17597969..17599564-chr11:17601245..17604128,2	K562	blood:
14	chr11:17569821..17570438-chr11:17586271..17587120,2	MCF-7	breast:
15	chr11:17563988..17566643-chr11:17568666..17571231,2	MCF-7	breast:
16	chr11:17550003..17552043-chr11:17563166..17565257,2	K562	blood:
17	chr11:17595636..17597692-chr11:17599938..17601981,3	K562	blood:
18	chr11:17558247..17559969-chr11:17568227..17570175,2	K562	blood:
19	chr11:17578365..17580159-chr11:17580246..17582171,2	MCF-7	breast:
20	chr11:17579575..17581891-chr11:17582600..17585148,3	K562	blood:
21	chr11:17578365..17580159-chr11:17580246..17582171,2	MCF-7	breast:
22	chr11:17573695..17575515-chr11:17575864..17578594,2	K562	blood:
23	chr11:17573988..17575798-chr11:17578729..17580759,2	K562	blood:
24	chr11:17554291..17557125-chr11:17558715..17560348,2	MCF-7	breast:
25	chr11:17594662..17597692-chr11:17599938..17601708,3	K562	blood:
26	chr11:17584725..17586615-chr11:17597092..17599857,2	MCF-7	breast:
27	chr11:17588922..17590478-chr11:17766034..17768818,2	K562	blood:
28	chr11:17569821..17570438-chr11:17586271..17587120,2	MCF-7	breast:
29	chr11:17557311..17560136-chr11:17561870..17563782,2	K562	blood:

No data

Variant related genes	Relation type
OTOG	TF binding region
USH1C	TF binding region
OTOG	CpG island
USH1C	CpG island
ENSG00000006611	chromatin interactions
ENSG00000188162	chromatin interactions

Extended variants
information (count: 1669 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1669 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2237957	chr11:17559018-17559019	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539488179	chr11:17559031-17559032	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs147094360	chr11:17559032-17559033	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs552095097	chr11:17559045-17559046	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs531499339	chr11:17559057-17559058	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549614143	chr11:17559119-17559120	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138419282	chr11:17559152-17559153	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530147764	chr11:17559168-17559169	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs17715485	chr11:17559220-17559221	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs2237956	chr11:17559261-17559262	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs534155937	chr11:17559298-17559299	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552277634	chr11:17559362-17559363	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs185779154	chr11:17559453-17559454	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192511699	chr11:17559488-17559489	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs368184633	chr11:17559498-17559499	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs78286956	chr11:17559499-17559500	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs4757540	chr11:17559509-17559510	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs181848274	chr11:17559520-17559521	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs111938463	chr11:17559548-17559549	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs75350653	chr11:17559590-17559591	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143442042	chr11:17559592-17559593	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs186001211	chr11:17559596-17559597	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs112716622	chr11:17559615-17559616	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs557468040	chr11:17559616-17559617	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575963828	chr11:17559621-17559622	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs78730869	chr11:17559633-17559634	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561565333	chr11:17559722-17559723	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs529006326	chr11:17559739-17559740	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs117175979	chr11:17559777-17559778	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112297991	chr11:17559796-17559797	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs113588923	chr11:17559808-17559809	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs535662554	chr11:17559892-17559893	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs527780675	chr11:17559904-17559905	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552567965	chr11:17559978-17559979	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190415724	chr11:17560047-17560048	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553636388	chr11:17560052-17560053	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374034585	chr11:17560105-17560106	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550468265	chr11:17560109-17560110	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs972676	chr11:17560127-17560128	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs147993618	chr11:17560137-17560138	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs182786537	chr11:17560138-17560139	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs559819060	chr11:17560217-17560218	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs188296818	chr11:17560218-17560219	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539140776	chr11:17560223-17560224	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs141776160	chr11:17560313-17560314	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575601134	chr11:17560328-17560329	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs111648872	chr11:17560417-17560418	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs555200244	chr11:17560523-17560524	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs190983507	chr11:17560546-17560547	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs541267060	chr11:17560621-17560622	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17538400-17562200	Weak transcription	Small Intestine	intestine
2	chr11:17547200-17563200	Genic enhancers	Fetal Intestine Small	intestine
3	chr11:17553600-17561800	Weak transcription	Gastric	stomach
4	chr11:17553600-17562200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr11:17553800-17563200	Weak transcription	Colonic Mucosa	Colon
6	chr11:17555400-17560400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr11:17555800-17562400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr11:17558000-17563400	Weak transcription	Hela-S3	cervix
9	chr11:17558200-17559800	Enhancers	Stomach Mucosa	stomach
10	chr11:17558400-17563200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr11:17558800-17562200	Genic enhancers	Fetal Intestine Large	intestine
12	chr11:17559000-17561800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr11:17559600-17560600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:17559800-17560200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr11:17559800-17562000	Weak transcription	Stomach Mucosa	stomach
16	chr11:17560200-17560600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr11:17560200-17562200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr11:17560400-17562600	Enhancers	Duodenum Mucosa	Duodenum
19	chr11:17560600-17560800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:17560800-17562000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:17561800-17562200	Enhancers	Gastric	stomach
22	chr11:17561800-17562800	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr11:17561800-17563000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr11:17562000-17564000	Enhancers	Stomach Mucosa	stomach
25	chr11:17562000-17565200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr11:17562200-17562400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr11:17562200-17562400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr11:17562200-17562400	Transcr. at gene 5' and 3'	Fetal Intestine Large	intestine
29	chr11:17562200-17564400	Weak transcription	Gastric	stomach
30	chr11:17562400-17562600	Enhancers	Small Intestine	intestine
31	chr11:17562400-17562800	Flanking Active TSS	Fetal Intestine Large	intestine
32	chr11:17562400-17564400	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr11:17562400-17566200	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr11:17562600-17562800	Flanking Active TSS	Duodenum Mucosa	Duodenum
35	chr11:17562600-17565000	Enhancers	A549	lung
36	chr11:17562800-17563200	Active TSS	Duodenum Mucosa	Duodenum
37	chr11:17562800-17563200	Enhancers	Fetal Intestine Large	intestine
38	chr11:17562800-17563600	Enhancers	HepG2	liver
39	chr11:17563000-17563400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr11:17563000-17563800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
41	chr11:17563000-17564000	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr11:17563200-17563400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr11:17563200-17563400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
44	chr11:17563200-17563600	Flanking Active TSS	Duodenum Mucosa	Duodenum
45	chr11:17563200-17563800	Enhancers	Colonic Mucosa	Colon
46	chr11:17563200-17563800	Flanking Active TSS	Fetal Intestine Large	intestine
47	chr11:17563200-17564400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:17563200-17565200	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr11:17563200-17566200	Active TSS	Rectal Smooth Muscle	rectum
50	chr11:17563400-17563600	Flanking Active TSS	Fetal Intestine Small	intestine

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