Variant report

Variant	esv1829886
Chromosome Location	chr11:5374268-5386668
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:5385003-5385179	K562	blood:	n/a	n/a
2	BHLHE40	chr11:5383352-5383583	K562	blood:	n/a	n/a
3	CEBPB	chr11:5385420-5385826	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr11:5386068-5386362	IMR90	lung:	n/a	n/a
5	CEBPB	chr11:5386039-5386374	Hela-S3	cervix:	n/a	n/a
6	EP300	chr11:5385247-5385950	SK-N-SH	brain:	n/a	chr11:5385847-5385861 chr11:5385634-5385641
7	EP300	chr11:5383298-5383498	K562	blood:	n/a	n/a
8	EP300	chr11:5385487-5385780	Hela-S3	cervix:	n/a	chr11:5385634-5385641
9	EP300	chr11:5385079-5385194	K562	blood:	n/a	n/a
10	EP300	chr11:5383370-5383809	Hela-S3	cervix:	n/a	n/a
11	FOS	chr11:5385398-5386116	HUVEC	blood vessel:	n/a	n/a
12	FOSL2	chr11:5385411-5385866	SK-N-SH	brain:	n/a	n/a
13	GATA2	chr11:5383292-5384109	HUVEC	blood vessel:	n/a	chr11:5383785-5383792 chr11:5383479-5383486 chr11:5383785-5383795 chr11:5383717-5383738 chr11:5383783-5383792 chr11:5383780-5383796 chr11:5383785-5383792 chr11:5383782-5383796 chr11:5383778-5383799 chr11:5383785-5383792 chr11:5383783-5383793 chr11:5383479-5383489
14	GATA2	chr11:5385114-5386027	HUVEC	blood vessel:	n/a	chr11:5385569-5385577
15	GATA3	chr11:5383278-5384003	SK-N-SH	brain:	n/a	chr11:5383785-5383792 chr11:5383479-5383486 chr11:5383785-5383795 chr11:5383717-5383738 chr11:5383783-5383792 chr11:5383780-5383796 chr11:5383785-5383792 chr11:5383778-5383799 chr11:5383785-5383792 chr11:5383783-5383793 chr11:5383479-5383489
16	GATA3	chr11:5385242-5386018	SK-N-SH	brain:	n/a	chr11:5385569-5385577
17	GATA3	chr11:5385315-5385957	SK-N-SH	brain:	n/a	chr11:5385569-5385577
18	GATA3	chr11:5383289-5383955	SK-N-SH	brain:	n/a	chr11:5383785-5383792 chr11:5383479-5383486 chr11:5383785-5383795 chr11:5383717-5383738 chr11:5383783-5383792 chr11:5383780-5383796 chr11:5383785-5383792 chr11:5383778-5383799 chr11:5383785-5383792 chr11:5383783-5383793 chr11:5383479-5383489
19	JUN	chr11:5385435-5385821	HUVEC	blood vessel:	n/a	n/a
20	JUND	chr11:5385360-5385986	SK-N-SH	brain:	n/a	n/a
21	MAFF	chr11:5384961-5385273	K562	blood:	n/a	n/a
22	MAFK	chr11:5384996-5385251	K562	blood:	n/a	n/a
23	MAFK	chr11:5384515-5384609	IMR90	lung:	n/a	n/a
24	MAZ	chr11:5385116-5385238	K562	blood:	n/a	n/a
25	MEF2A	chr11:5384926-5385315	K562	blood:	n/a	chr11:5385140-5385154 chr11:5385035-5385050 chr11:5384996-5385017 chr11:5385139-5385154 chr11:5385135-5385156 chr11:5385034-5385050 chr11:5385138-5385153 chr11:5385142-5385151 chr11:5385038-5385047 chr11:5385142-5385153
26	MEF2A	chr11:5384940-5385281	K562	blood:	n/a	chr11:5385140-5385154 chr11:5385035-5385050 chr11:5384996-5385017 chr11:5385139-5385154 chr11:5385135-5385156 chr11:5385034-5385050 chr11:5385138-5385153 chr11:5385142-5385151 chr11:5385038-5385047 chr11:5385142-5385153
27	NFIC	chr11:5385245-5385992	SK-N-SH	brain:	n/a	n/a
28	NFIC	chr11:5385414-5385812	SK-N-SH	brain:	n/a	n/a
29	PBX3	chr11:5385442-5386002	SK-N-SH	brain:	n/a	n/a
30	PBX3	chr11:5385300-5385828	SK-N-SH	brain:	n/a	n/a
31	POLR2A	chr11:5383391-5383426	K562	blood:	n/a	n/a
32	POLR2A	chr11:5386224-5386294	ProgFib	skin:	n/a	n/a
33	POLR2A	chr11:5385601-5385607	K562	blood:	n/a	n/a
34	POLR2A	chr11:5383749-5383984	HCT-116	colon:	n/a	n/a
35	POLR2A	chr11:5378510-5378730	K562	blood:	n/a	n/a
36	POLR2A	chr11:5385491-5387414	IMR90	lung:	n/a	n/a
37	POLR2A	chr11:5376315-5376370	Gliobla	brain:	n/a	n/a
38	POLR2A	chr11:5386541-5386615	K562	blood:	n/a	n/a
39	POLR2A	chr11:5386295-5386327	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr11:5385431-5385745	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr11:5382541-5382549	K562	blood:	n/a	n/a
42	POLR2A	chr11:5385157-5385199	K562	blood:	n/a	n/a
43	POLR2A	chr11:5385409-5385756	K562	blood:	n/a	n/a
44	POLR2A	chr11:5375723-5376010	HCT-116	colon:	n/a	n/a
45	POLR2A	chr11:5386627-5386706	K562	blood:	n/a	n/a
46	POLR2A	chr11:5379158-5379322	K562	blood:	n/a	n/a
47	PRDM1	chr11:5383345-5383590	Hela-S3	cervix:	n/a	chr11:5383479-5383494 chr11:5383434-5383449
48	RCOR1	chr11:5383274-5383676	K562	blood:	n/a	n/a
49	RCOR1	chr11:5385493-5385773	Hela-S3	cervix:	n/a	n/a
50	RXRA	chr11:5385409-5385804	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5384517-5384567	CMK	blood:	n/a
2	chr11:5384517-5384567	CMK	blood:	n/a
3	chr11:5384517-5384567	HAEpiC	amniotic membrane:	n/a
4	chr11:5384517-5384567	HMEC	breast:	n/a
5	chr11:5384517-5384567	PFSK-1	brain:	n/a
6	chr11:5384517-5384567	HEEpiC	esophagus:	n/a
7	chr11:5384517-5384567	HL-60	blood:	n/a
8	chr11:5384517-5384567	SKMC	muscle:	n/a
9	chr11:5384517-5384567	HepG2	liver:	n/a
10	chr11:5384517-5384567	PrEC	prostate:	n/a
11	chr11:5384517-5384567	SK-N-SH_RA	brain:	n/a
12	chr11:5384517-5384567	HCF	heart:	n/a
13	chr11:5384517-5384567	SAEC	small airway:	n/a
14	chr11:5384517-5384567	Hepatocyte	liver:	n/a
15	chr11:5384517-5384567	GM12878	blood:	n/a
16	chr11:5384517-5384567	NH-A	brain:	n/a
17	chr11:5384517-5384567	AG04450	lung:	fetal
18	chr11:5384517-5384567	NHBE	bronchial:	n/a
19	chr11:5384517-5384567	AG09319	gingival:	n/a
20	chr11:5384517-5384567	HRE	kidney:	n/a
21	chr11:5384517-5384567	Caco-2	colon:	n/a
22	chr11:5384517-5384567	HCPEpiC	choroid plexus:	n/a
23	chr11:5384517-5384567	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:5384517-5384567	BE2_C	brain:	n/a
25	chr11:5384517-5384567	NB4	blood:	n/a
26	chr11:5384517-5384567	ovcar-3	ovarian:	n/a
27	chr11:5384517-5384567	H1-hESC	embryonic stem cell:	embryo
28	chr11:5384517-5384567	AG09309	skin:	n/a
29	chr11:5384517-5384567	HCT-116	colon:	n/a
30	chr11:5384517-5384567	IMR90	lung:	fetal
31	chr11:5384517-5384567	A549	lung:	n/a
32	chr11:5384517-5384567	HEK293	kidney:	embryo
33	chr11:5384517-5384567	MCF-7	breast:	n/a
34	chr11:5384517-5384567	GM12892	blood:	n/a
35	chr11:5384517-5384567	HCM	heart:	n/a
36	chr11:5384517-5384567	GM19239	blood:	n/a
37	chr11:5384517-5384567	PANC-1	pancreas:	n/a
38	chr11:5384517-5384567	HUVEC	blood vessel:	n/a
39	chr11:5384517-5384567	U87	brain:	n/a
40	chr11:5384517-5384567	RPTEC	kidney:	n/a
41	chr11:5384517-5384567	ECC-1	luminal epithelium:	n/a
42	chr11:5384517-5384567	GM06990	blood:	n/a
43	chr11:5384517-5384567	AG04449	skin:	fetal
44	chr11:5384517-5384567	BJ	skin:	n/a
45	chr11:5384517-5384567	NHDF-neo	bronchial:	n/a
46	chr11:5384517-5384567	Jurkat	blood:	n/a
47	chr11:5384517-5384567	HRCEpiC	kidney:	n/a
48	chr11:5384517-5384567	HIPEpiC	eye:	n/a
49	chr11:5384517-5384567	HNPCEpiC	eye:	n/a
50	chr11:5384517-5384567	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5381283..5382803-chr17:41464203..41466198,2	MCF-7	breast:
2	chr11:5381283..5382803-chr11:62607627..62609148,3	K562	blood:
3	chr10:103124107..103125128-chr11:5382283..5382803,4	HCT-116	colon:
4	chr11:5382283..5382803-chr3:73159935..73160621,4	MCF-7	breast:
5	chr11:5381283..5382803-chr17:41463815..41467678,7	K562	blood:
6	chr11:5381283..5382803-chr17:41398716..41402368,7	K562	blood:
7	chr11:5385575..5387754-chr11:5392449..5394884,2	K562	blood:
8	chr11:5382303..5383283-chr3:73159952..73160632,4	NB4	blood:
9	chr11:5382803..5384303-chr11:62607722..62610627,2	K562	blood:
10	chr11:5381283..5382803-chr3:73158604..73161608,4	K562	blood:
11	chr11:5381283..5382783-chr17:41380312..41381821,2	MCF-7	breast:
12	chr11:5384124..5385767-chr11:5387283..5389565,2	K562	blood:
13	chr11:5381283..5382783-chr17:41464201..41465702,2	MCF-7	breast:
14	chr11:5382283..5383283-chr3:73160073..73160610,2	Hela-S3	cervix:
15	chr11:5381283..5382803-chr3:73159067..73161609,3	K562	blood:
16	chr11:5381283..5382783-chr17:41380573..41383525,2	MCF-7	breast:
17	chr11:5381303..5382803-chr11:62607635..62609203,2	MCF-7	breast:
18	chr11:5381283..5382803-chr17:41463769..41467201,6	K562	blood:
19	chr11:5382283..5382803-chr2:16124613..16125133,2	MCF-7	breast:
20	chr10:103124128..103124630-chr11:5382283..5382783,2	MCF-7	breast:
21	chr11:5382283..5382803-chr11:62608622..62609624,4	MCF-7	breast:
22	chr11:5381283..5382803-chr5:133457468..133458988,2	K562	blood:
23	chr11:5381283..5382803-chr11:61276233..61277753,2	K562	blood:
24	chr11:5382283..5383303-chr11:62608619..62609221,10	Hela-S3	cervix:
25	chr11:5382283..5382803-chr11:62608620..62609139,4	MCF-7	breast:
26	11:4789513-4794705..11:5380014-5384338	H1-hESC	embryonic stem cell:	embryo
27	chr11:5382283..5382803-chr18:21285383..21285903,2	Hela-S3	cervix:
28	chr11:5382283..5383303-chr3:73159935..73160633,6	HCT-116	colon:
29	chr11:5381283..5382803-chr3:73159944..73161618,3	MCF-7	breast:
30	chr1:212997378..212997898-chr11:5382283..5382803,2	HCT-116	colon:
31	chr11:5151510..5153269-chr11:5386500..5388516,2	K562	blood:
32	chr11:5382283..5382803-chr11:62608619..62609221,11	HCT-116	colon:
33	chr11:5381283..5382803-chr17:41380385..41382126,2	K562	blood:
34	chr11:5151592..5153371-chr11:5383918..5386236,2	K562	blood:
35	11:5250847-5268367..11:5380014-5384338	H1-hESC	embryonic stem cell:	embryo

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51B6-2	chr11:5383845-5384079	NONHSAT017681

Variant related genes	Relation type
ENSG00000230087	TF binding region
ENSG00000236248	TF binding region
ENSG00000230087	CpG island
ENSG00000236248	CpG island
ENSG00000223609	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000188069	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000204950	chromatin interactions

Extended variants
information (count: 836 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4243957	chr11:5374268-5374269	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs4243958	chr11:5374303-5374304	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs556017659	chr11:5374307-5374308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4243959	chr11:5374330-5374331	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs538531755	chr11:5374354-5374355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4494328	chr11:5374355-5374356	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs115568951	chr11:5374392-5374393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545501054	chr11:5374395-5374396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114398603	chr11:5374400-5374401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572202857	chr11:5374435-5374436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114837819	chr11:5374441-5374442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561145755	chr11:5374457-5374458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146630318	chr11:5374472-5374473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78526400	chr11:5374476-5374477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564522858	chr11:5374513-5374514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4345997	chr11:5374514-5374515	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs546354469	chr11:5374519-5374520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571537841	chr11:5374533-5374534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547089859	chr11:5374541-5374542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566707374	chr11:5374543-5374544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184060713	chr11:5374556-5374557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188645327	chr11:5374570-5374571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191700505	chr11:5374585-5374586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs118080487	chr11:5374586-5374587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538119168	chr11:5374610-5374611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182465471	chr11:5374614-5374615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556928497	chr11:5374684-5374685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10606125	chr11:5374690-5374691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142751494	chr11:5374700-5374701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571645606	chr11:5374737-5374738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4369438	chr11:5374743-5374744	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs4347419	chr11:5374786-5374787	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs572407497	chr11:5374787-5374788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536774779	chr11:5374802-5374803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116762758	chr11:5374806-5374807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200931846	chr11:5374827-5374828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576221705	chr11:5374840-5374841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4492850	chr11:5374857-5374858	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs117602096	chr11:5374870-5374871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143768576	chr11:5374898-5374899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186872323	chr11:5374902-5374903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573480214	chr11:5374927-5374928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191762900	chr11:5374958-5374959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2723387	chr11:5375091-5375092	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548278485	chr11:5375138-5375139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117191859	chr11:5375147-5375148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57115004	chr11:5375153-5375154	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs74772552	chr11:5375155-5375156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576330815	chr11:5375166-5375167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572010154	chr11:5375182-5375183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	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
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5365600-5382600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:5370200-5376000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:5373000-5376800	Strong transcription	K562	blood
4	chr11:5376000-5376800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:5376800-5382600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:5376800-5382600	Weak transcription	K562	blood
7	chr11:5382600-5383200	Strong transcription	K562	blood
8	chr11:5382600-5383600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:5382600-5384000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr11:5382800-5384000	Enhancers	Hela-S3	cervix
11	chr11:5382800-5384200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:5382800-5385600	Enhancers	NHDF-Ad	bronchial
13	chr11:5383000-5386600	Enhancers	NH-A	brain
14	chr11:5383000-5387400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:5383200-5383400	Enhancers	Osteobl	bone
16	chr11:5383200-5383800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr11:5383200-5383800	Enhancers	NHLF	lung
18	chr11:5383200-5388400	Genic enhancers	K562	blood
19	chr11:5383400-5383600	Enhancers	HUVEC	blood vessel
20	chr11:5383400-5383800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:5383400-5384200	Weak transcription	Osteobl	bone
22	chr11:5383800-5384200	Weak transcription	NHLF	lung
23	chr11:5383800-5384800	Weak transcription	HUVEC	blood vessel
24	chr11:5383800-5385000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:5383800-5385000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr11:5384000-5385000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr11:5384000-5385400	Weak transcription	Hela-S3	cervix
28	chr11:5384200-5391200	Enhancers	NHLF	lung
29	chr11:5384200-5391200	Enhancers	Osteobl	bone
30	chr11:5384800-5389600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr11:5384800-5389600	Enhancers	HUVEC	blood vessel
32	chr11:5385000-5386800	Enhancers	Muscle Satellite Cultured Cells	--
33	chr11:5385000-5386800	Enhancers	HSMMtube	muscle
34	chr11:5385000-5387400	Enhancers	HSMM	muscle
35	chr11:5385000-5389000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr11:5385000-5389600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:5385000-5391400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:5385200-5385600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:5385400-5385800	Enhancers	Hela-S3	cervix
40	chr11:5385400-5385800	Enhancers	HMEC	breast
41	chr11:5385600-5386000	Flanking Active TSS	NHDF-Ad	bronchial
42	chr11:5385600-5388800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:5385800-5388000	Weak transcription	Hela-S3	cervix
44	chr11:5386000-5391200	Enhancers	NHDF-Ad	bronchial
45	chr11:5386400-5387200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:5386600-5386800	Flanking Active TSS	NH-A	brain

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