Variant report

Variant	esv3493111
Chromosome Location	chr11:71850822-71893073
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	ARID3A	chr11:71863826-71864078	K562	blood:	n/a	n/a
2	ARID3A	chr11:71855048-71855363	K562	blood:	n/a	n/a
3	ATF1	chr11:71855078-71855400	K562	blood:	n/a	n/a
4	ATF1	chr11:71852182-71852593	K562	blood:	n/a	n/a
5	ATF3	chr11:71854980-71855362	K562	blood:	n/a	n/a
6	BACH1	chr11:71855102-71855389	K562	blood:	n/a	chr11:71855183-71855197
7	BACH1	chr11:71855082-71855372	H1-hESC	embryonic stem cell:	n/a	chr11:71855183-71855197
8	BATF	chr11:71855059-71855340	GM12878	blood:	n/a	n/a
9	BCLAF1	chr11:71855051-71855430	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:71874120-71874221	K562	blood:	n/a	n/a
11	BHLHE40	chr11:71855065-71855353	K562	blood:	n/a	n/a
12	CBX3	chr11:71876267-71876538	K562	blood:	n/a	n/a
13	CBX3	chr11:71876288-71876548	K562	blood:	n/a	n/a
14	CEBPB	chr11:71885020-71885043	K562	blood:	n/a	n/a
15	CEBPB	chr11:71856053-71856684	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr11:71885580-71885641	K562	blood:	n/a	chr11:71885590-71885601 chr11:71885589-71885602 chr11:71885589-71885600
17	CEBPB	chr11:71856236-71856591	A549	lung:	n/a	n/a
18	CEBPB	chr11:71856194-71856488	A549	lung:	n/a	n/a
19	CEBPB	chr11:71852144-71852555	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:71884923-71885216	IMR90	lung:	n/a	n/a
21	CEBPB	chr11:71885414-71885768	HepG2	liver:	n/a	chr11:71885590-71885601 chr11:71885589-71885602 chr11:71885589-71885600
22	CEBPB	chr11:71851315-71851666	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:71850861-71851079	K562	blood:	n/a	chr11:71850978-71850991
24	CEBPB	chr11:71871429-71871762	IMR90	lung:	n/a	n/a
25	CEBPB	chr11:71884912-71885998	Hela-S3	cervix:	n/a	chr11:71885590-71885601 chr11:71885589-71885602 chr11:71885589-71885600
26	CEBPB	chr11:71871545-71871605	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:71889113-71889199	K562	blood:	n/a	chr11:71889130-71889143
28	CEBPB	chr11:71865867-71866166	K562	blood:	n/a	n/a
29	CEBPB	chr11:71856124-71856610	IMR90	lung:	n/a	n/a
30	CEBPD	chr11:71863720-71864192	K562	blood:	n/a	n/a
31	CEBPD	chr11:71863755-71864253	K562	blood:	n/a	n/a
32	CHD2	chr11:71885399-71885770	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr11:71856201-71856502	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr11:71855040-71855320	A549	lung:	n/a	n/a
35	CTCF	chr11:71892800-71892950	NB4	blood:	n/a	chr11:71892904-71892925 chr11:71892910-71892926
36	CTCF	chr11:71892806-71893024	ProgFib	skin:	n/a	chr11:71892904-71892925 chr11:71892910-71892926
37	CTCF	chr11:71853895-71854310	A549	lung:	n/a	chr11:71854101-71854122
38	CTCF	chr11:71855160-71855310	GM06990	blood:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
39	CTCF	chr11:71892750-71892964	A549	lung:	n/a	chr11:71892904-71892925 chr11:71892910-71892926
40	CTCF	chr11:71854954-71855007	GM12891	blood:	n/a	n/a
41	CTCF	chr11:71854043-71854175	H1-hESC	embryonic stem cell:	n/a	chr11:71854101-71854122
42	CTCF	chr11:71855520-71855670	GM12868	blood:	n/a	n/a
43	CTCF	chr11:71892880-71893030	HMEC	breast:	n/a	chr11:71892904-71892925 chr11:71892910-71892926
44	CTCF	chr11:71892792-71892995	HepG2	liver:	n/a	chr11:71892904-71892925 chr11:71892910-71892926
45	CTCF	chr11:71855025-71855471	GM12878	blood:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
46	CTCF	chr11:71855160-71855310	GM12867	blood:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
47	CTCF	chr11:71854640-71854790	HCM	heart:	n/a	n/a
48	CTCF	chr11:71892800-71892950	HPAF	blood vessel:	n/a	chr11:71892904-71892925 chr11:71892910-71892926
49	CTCF	chr11:71854936-71855042	GM13976	blood:	n/a	n/a
50	CTCF	chr11:71854037-71854178	MCF-7	breast:	n/a	chr11:71854101-71854122

No.	Distal block	Cell Line	Cell type
1	chr11:71821479..71826547-chr11:71844956..71851162,6	K562	blood:
2	chr11:71853125..71854944-chr11:71891324..71892926,2	MCF-7	breast:
3	chr11:71870250..71872525-chr11:71873469..71876026,2	K562	blood:
4	chr11:71817497..71819718-chr11:71852568..71855106,2	MCF-7	breast:
5	chr11:71849346..71852118-chr11:71862000..71864280,2	K562	blood:
6	chr11:71850218..71852679-chr11:71853502..71855781,2	MCF-7	breast:
7	chr11:71790289..71792408-chr11:71893051..71895106,2	K562	blood:
8	chr11:71822984..71825234-chr11:71889608..71891986,2	K562	blood:
9	chr11:71814518..71815081-chr11:71892378..71893328,2	MCF-7	breast:
10	chr11:71887728..71891423-chr11:71933064..71936414,3	MCF-7	breast:
11	chr11:71814495..71816095-chr11:71889921..71892170,2	MCF-7	breast:
12	chr11:71855220..71857768-chr11:71870927..71873588,3	K562	blood:
13	chr11:71853234..71854961-chr11:71893001..71894509,2	MCF-7	breast:
14	chr11:71726841..71727497-chr11:71854902..71855407,2	MCF-7	breast:
15	chr11:71808840..71811674-chr11:71882236..71884134,2	MCF-7	breast:
16	chr11:71688550..71689500-chr11:71854791..71855728,4	K562	blood:
17	chr11:71882037..71883991-chr11:71899030..71901488,2	K562	blood:
18	chr11:71851522..71853498-chr11:71890827..71892489,2	K562	blood:
19	chr11:71891814..71894783-chr11:71939408..71941980,2	MCF-7	breast:
20	chr11:71876184..71878568-chr11:71933790..71935887,2	K562	blood:
21	chr11:71851522..71853498-chr11:71890827..71892489,2	K562	blood:
22	chr11:71823336..71825069-chr11:71869762..71871942,2	K562	blood:
23	chr11:71822348..71825348-chr11:71852319..71854832,3	MCF-7	breast:
24	chr11:71855220..71857768-chr11:71870927..71873588,3	K562	blood:
25	chr11:71853234..71854961-chr11:71893001..71894509,2	MCF-7	breast:
26	chr11:71853125..71854944-chr11:71891324..71892926,2	MCF-7	breast:
27	chr11:71870250..71872525-chr11:71873469..71876026,2	K562	blood:
28	chr11:71848622..71850667-chr11:71854281..71856804,2	MCF-7	breast:
29	chr11:71802059..71803123-chr11:71892536..71893396,4	MCF-7	breast:
30	chr11:71814410..71815140-chr11:71854813..71855316,2	MCF-7	breast:
31	chr11:71736115..71737039-chr11:71854770..71856004,4	MCF-7	breast:
32	chr11:71822765..71825342-chr11:71891494..71894881,3	MCF-7	breast:
33	chr11:71812901..71816436-chr11:71891648..71895235,3	MCF-7	breast:
34	chr11:71821717..71826052-chr11:71851780..71856774,7	MCF-7	breast:
35	chr11:71736299..71737011-chr11:71854769..71855288,2	K562	blood:
36	chr11:71868137..71870587-chr11:71874511..71876205,2	K562	blood:
37	chr11:71821644..71823933-chr11:71854873..71856774,3	MCF-7	breast:
38	chr11:71820348..71823346-chr11:71883678..71885281,2	MCF-7	breast:
39	chr11:71892089..71899767-chr11:71932198..71938426,12	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHOX2A-1	chr11:71874366-71874423	ENSG00000204971.3

Variant related genes	Relation type
ENSG00000255860	TF binding region
ENSG00000256518	TF binding region
ENSG00000165458	chromatin interactions
ENSG00000110203	chromatin interactions
ENSG00000110200	chromatin interactions
ENSG00000184154	chromatin interactions
ENSG00000137497	chromatin interactions
ENSG00000238768	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000110195	chromatin interactions
ENSG00000256518	chromatin interactions

Extended variants
information (count: 1719 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1719 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369675505	chr11:71850823-71850824	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs373588555	chr11:71850828-71850829	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145575368	chr11:71850829-71850830	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs189330558	chr11:71850830-71850831	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372529845	chr11:71850834-71850835	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs375597867	chr11:71850850-71850851	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs370372415	chr11:71850855-71850856	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs374758856	chr11:71850856-71850857	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs368765894	chr11:71850896-71850897	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs180805714	chr11:71850900-71850901	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs540813817	chr11:71850914-71850915	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552875775	chr11:71850928-71850929	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577511195	chr11:71850939-71850940	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs544717033	chr11:71850961-71850962	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs376350645	chr11:71850967-71850968	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563302340	chr11:71850974-71850975	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs571669221	chr11:71851006-71851007	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs113984857	chr11:71851087-71851088	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542728160	chr11:71851090-71851091	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs560930151	chr11:71851101-71851102	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs117741139	chr11:71851116-71851117	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs548008242	chr11:71851146-71851147	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs560129970	chr11:71851187-71851188	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11235449	chr11:71851199-71851200	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs184277272	chr11:71851208-71851209	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56777831	chr11:71851305-71851306	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs71052851	chr11:71851344-71851345	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570056447	chr11:71851345-71851346	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs514428	chr11:71851346-71851347	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188669908	chr11:71851365-71851366	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554567633	chr11:71851397-71851398	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181731619	chr11:71851410-71851411	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs186774188	chr11:71851470-71851471	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs118013879	chr11:71851507-71851508	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs192535068	chr11:71851531-71851532	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs623585	chr11:71851567-71851568	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs556947584	chr11:71851568-71851569	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs565039242	chr11:71851618-71851619	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538322	chr11:71851663-71851664	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs192029449	chr11:71851724-71851725	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561013895	chr11:71851746-71851747	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572966543	chr11:71851748-71851749	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11235450	chr11:71851762-71851763	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559825389	chr11:71851765-71851766	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375291613	chr11:71851773-71851774	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540290846	chr11:71851797-71851798	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs559991746	chr11:71851800-71851801	Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs533338784	chr11:71851803-71851804	Enhancers Flanking Active TSS Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs182248270	chr11:71851905-71851906	Enhancers Flanking Active TSS Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs138828584	chr11:71851930-71851931	Enhancers Flanking Active TSS Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	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
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71834400-71851000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:71846800-71853400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr11:71847400-71851000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:71847600-71851000	Weak transcription	NH-A	brain
5	chr11:71847800-71851400	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
6	chr11:71848000-71852000	Weak transcription	HSMMtube	muscle
7	chr11:71848000-71852600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:71848400-71854600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr11:71848800-71851600	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
10	chr11:71849200-71851000	Weak transcription	Fetal Intestine Large	intestine
11	chr11:71849200-71852800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr11:71849800-71853600	Genic enhancers	Primary monocytes fromperipheralblood	blood
13	chr11:71850000-71851000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:71850000-71851200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:71850400-71851000	Weak transcription	Primary B cells from cord blood	blood
16	chr11:71850400-71851200	Enhancers	Esophagus	oesophagus
17	chr11:71850400-71852000	Enhancers	NHEK	skin
18	chr11:71850600-71851800	Strong transcription	Spleen	Spleen
19	chr11:71850600-71852400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:71850600-71852400	Enhancers	HSMM	muscle
21	chr11:71850600-71853400	Enhancers	NHDF-Ad	bronchial
22	chr11:71850800-71852000	Enhancers	Muscle Satellite Cultured Cells	--
23	chr11:71850800-71852400	Enhancers	Osteobl	bone
24	chr11:71850800-71853000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:71850800-71853200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:71850800-71853400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr11:71850800-71853400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr11:71850800-71853600	Enhancers	Hela-S3	cervix
29	chr11:71850800-71856200	Enhancers	HMEC	breast
30	chr11:71851000-71851200	Enhancers	Primary B cells from cord blood	blood
31	chr11:71851000-71851200	Enhancers	Fetal Intestine Large	intestine
32	chr11:71851000-71851200	Enhancers	Placenta Amnion	Placenta Amnion
33	chr11:71851000-71851200	Enhancers	A549	lung
34	chr11:71851000-71851200	Enhancers	NHLF	lung
35	chr11:71851000-71851800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr11:71851000-71852000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr11:71851000-71852000	Enhancers	NH-A	brain
38	chr11:71851000-71852800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr11:71851000-71853200	Enhancers	Placenta	Placenta
40	chr11:71851000-71853400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr11:71851200-71851800	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr11:71851200-71851800	Weak transcription	NHLF	lung
43	chr11:71851200-71852400	Weak transcription	Primary B cells from cord blood	blood
44	chr11:71851200-71852400	Weak transcription	A549	lung
45	chr11:71851200-71856200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr11:71851400-71853400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
47	chr11:71851600-71853200	Genic enhancers	Monocytes-CD14+_RO01746	blood
48	chr11:71851800-71852000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr11:71851800-71852200	Weak transcription	Spleen	Spleen
50	chr11:71851800-71852600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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