Variant report

Variant	esv3439523
Chromosome Location	chr11:71279704-71284002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:43 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr11:71281541-71282202	GM12878	blood:	n/a	n/a
2	BCL3	chr11:71281522-71282063	GM12878	blood:	n/a	n/a
3	CTCF	chr11:71282880-71283030	Caco-2	colon:	n/a	n/a
4	CTCF	chr11:71279660-71279810	MCF-7	breast:	n/a	n/a
5	CTCF	chr11:71279661-71279749	MCF-7	breast:	n/a	n/a
6	CTCF	chr11:71279653-71279762	MCF-7	breast:	n/a	n/a
7	CTCF	chr11:71282940-71283090	Caco-2	colon:	n/a	n/a
8	CTCF	chr11:71280593-71280657	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr11:71279620-71279770	NHEK	skin:	n/a	n/a
10	CTCF	chr11:71279657-71279768	MCF-7	breast:	n/a	n/a
11	CTCF	chr11:71279680-71279740	MCF-7	breast:	n/a	n/a
12	CTCF	chr11:71279659-71279765	MCF-7	breast:	n/a	n/a
13	CTCF	chr11:71279640-71279790	MCF-7	breast:	n/a	n/a
14	EP300	chr11:71279462-71279902	MCF-7	breast:	n/a	n/a
15	FOXA1	chr11:71279488-71279909	HepG2	liver:	n/a	n/a
16	FOXA1	chr11:71279506-71279753	HepG2	liver:	n/a	n/a
17	FOXA2	chr11:71279461-71279796	A549	lung:	n/a	n/a
18	FOXA2	chr11:71279486-71279724	HepG2	liver:	n/a	n/a
19	GATA2	chr11:71279383-71280187	SH-SY5Y	brain:	n/a	chr11:71279443-71279453
20	GATA3	chr11:71279246-71280070	MCF-7	breast:	n/a	chr11:71279443-71279453
21	GATA3	chr11:71279409-71280124	SH-SY5Y	brain:	n/a	chr11:71279443-71279453
22	GATA3	chr11:71279459-71280166	MCF-7	breast:	n/a	n/a
23	GATA3	chr11:71279929-71280028	MCF-7	breast:	n/a	n/a
24	GATA3	chr11:71279405-71280187	MCF-7	breast:	n/a	chr11:71279443-71279453
25	GATA3	chr11:71279557-71279726	MCF-7	breast:	n/a	n/a
26	HDAC2	chr11:71279493-71279890	MCF-7	breast:	n/a	n/a
27	HNF4A	chr11:71282845-71283189	HepG2	liver:	n/a	chr11:71283023-71283038
28	HNF4A	chr11:71282819-71283168	HepG2	liver:	n/a	chr11:71283023-71283038
29	MYC	chr11:71280875-71280890	H1-hESC	embryonic stem cell:	n/a	n/a
30	MYC	chr11:71282317-71282424	HUVEC	blood vessel:	n/a	n/a
31	MYC	chr11:71279680-71279719	MCF-7	breast:	n/a	n/a
32	MYC	chr11:71279777-71279975	MCF-7	breast:	n/a	n/a
33	MYC	chr11:71279722-71279772	MCF-7	breast:	n/a	n/a
34	NFATC1	chr11:71281510-71281903	GM12878	blood:	n/a	n/a
35	NFATC1	chr11:71281518-71282123	GM12878	blood:	n/a	n/a
36	NR2F2	chr11:71279489-71279934	MCF-7	breast:	n/a	n/a
37	NR2F2	chr11:71279502-71279791	MCF-7	breast:	n/a	n/a
38	PBX3	chr11:71281543-71282140	GM12878	blood:	n/a	n/a
39	SIN3AK20	chr11:71279254-71280325	MCF-7	breast:	n/a	n/a
40	STAT5A	chr11:71281635-71282070	GM12878	blood:	n/a	n/a
41	SUZ12	chr11:71281907-71282134	H1-hESC	embryonic stem cell:	n/a	n/a
42	TCF3	chr11:71281678-71281889	GM12878	blood:	n/a	n/a
43	ZNF217	chr11:71279578-71280185	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71282718-71282768	GM06990	blood:	n/a
2	chr11:71282370-71282420	K562	blood:	n/a
3	chr11:71282718-71282768	HRCEpiC	kidney:	n/a
4	chr11:71282718-71282768	Caco-2	colon:	n/a
5	chr11:71282370-71282420	CMK	blood:	n/a
6	chr11:71282370-71282420	HCT-116	colon:	n/a
7	chr11:71282718-71282768	PrEC	prostate:	n/a
8	chr11:71282718-71282768	IMR90	lung:	fetal
9	chr11:71282370-71282420	HMEC	breast:	n/a
10	chr11:71282370-71282420	LNCaP	prostate:	n/a
11	chr11:71282718-71282768	GM12878	blood:	n/a
12	chr11:71282718-71282768	HCM	heart:	n/a
13	chr11:71282370-71282420	HUVEC	blood vessel:	n/a
14	chr11:71282718-71282768	PANC-1	pancreas:	n/a
15	chr11:71282370-71282420	GM12891	blood:	n/a
16	chr11:71282718-71282768	BJ	skin:	n/a
17	chr11:71282718-71282768	HIPEpiC	eye:	n/a
18	chr11:71282370-71282420	T-47D	breast:	n/a
19	chr11:71282370-71282420	NH-A	brain:	n/a
20	chr11:71282370-71282420	BE2_C	brain:	n/a
21	chr11:71282718-71282768	HUVEC	blood vessel:	n/a
22	chr11:71282718-71282768	HCF	heart:	n/a
23	chr11:71282718-71282768	HMEC	breast:	n/a
24	chr11:71282370-71282420	A549	lung:	n/a
25	chr11:71282718-71282768	CMK	blood:	n/a
26	chr11:71282370-71282420	MCF-7	breast:	n/a
27	chr11:71282370-71282420	Caco-2	colon:	n/a
28	chr11:71282718-71282768	AG04449	skin:	fetal
29	chr11:71282370-71282420	NB4	blood:	n/a
30	chr11:71282718-71282768	ECC-1	luminal epithelium:	n/a
31	chr11:71282718-71282768	T-47D	breast:	n/a
32	chr11:71282718-71282768	SAEC	small airway:	n/a
33	chr11:71282370-71282420	ovcar-3	ovarian:	n/a
34	chr11:71282718-71282768	BE2_C	brain:	n/a
35	chr11:71282718-71282768	Hela-S3	cervix:	n/a
36	chr11:71282370-71282420	ECC-1	luminal epithelium:	n/a
37	chr11:71282370-71282420	SK-N-SH	brain:	n/a
38	chr11:71282718-71282768	AG09309	skin:	n/a
39	chr11:71282370-71282420	ProgFib	skin:	n/a
40	chr11:71282718-71282768	NHBE	bronchial:	n/a
41	chr11:71282370-71282420	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:71282718-71282768	H1-hESC	embryonic stem cell:	embryo
43	chr11:71282718-71282768	GM12892	blood:	n/a
44	chr11:71282718-71282768	SK-N-SH	brain:	n/a
45	chr11:71282370-71282420	AG09309	skin:	n/a
46	chr11:71282370-71282420	Hela-S3	cervix:	n/a
47	chr11:71282370-71282420	HL-60	blood:	n/a
48	chr11:71282718-71282768	ProgFib	skin:	n/a
49	chr11:71282718-71282768	MCF-7	breast:	n/a
50	chr11:71282370-71282420	IMR90	lung:	fetal

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71162651..71164294-chr11:71282060..71284159,2	K562	blood:
2	chr11:71158604..71160379-chr11:71280505..71283180,2	MCF-7	breast:
3	chr11:71272055..71274887-chr11:71280546..71282110,2	K562	blood:
4	chr11:71278628..71280477-chr11:71289049..71291000,2	MCF-7	breast:
5	chr11:71282448..71285837-chr11:71286010..71289392,3	MCF-7	breast:
6	chr11:71279845..71280406-chr11:71290008..71290749,2	MCF-7	breast:
7	chr11:71198072..71200599-chr11:71283906..71285709,2	MCF-7	breast:
8	chr11:71279425..71280036-chr11:71290519..71291383,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTAP5-10-1	chr11:71279726-71279980	NONHSAT022692

No data

Variant related genes	Relation type
ENSG00000248903	TF binding region
ENSG00000248903	CpG island
ENSG00000172893	chromatin interactions
ENSG00000249387	chromatin interactions
ENSG00000172890	chromatin interactions
ENSG00000254682	chromatin interactions

Extended variants
information (count: 272 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374350043	chr11:71279725-71279726	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs557413070	chr11:71279757-71279758	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs370246933	chr11:71279790-71279791	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs575583349	chr11:71279798-71279799	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs112936370	chr11:71279839-71279840	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs186393988	chr11:71279847-71279848	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs191202370	chr11:71279862-71279863	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs540392100	chr11:71279864-71279865	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs143753543	chr11:71279869-71279870	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs61890232	chr11:71279872-71279873	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs28710033	chr11:71279892-71279893	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs9651733	chr11:71279894-71279895	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs111962306	chr11:71279902-71279903	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs565081425	chr11:71279905-71279906	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs9651734	chr11:71279906-71279907	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs111350381	chr11:71279907-71279908	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs111351399	chr11:71279922-71279923	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs114510875	chr11:71279935-71279936	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs72475645	chr11:71279936-71279937	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs200834593	chr11:71279995-71279996	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532254830	chr11:71280018-71280019	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111626347	chr11:71280031-71280032	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs141928568	chr11:71280034-71280035	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559984723	chr11:71280051-71280052	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150828882	chr11:71280052-71280053	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547802813	chr11:71280065-71280066	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530275474	chr11:71280070-71280071	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78987639	chr11:71280089-71280090	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs566196067	chr11:71280092-71280093	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560685738	chr11:71280099-71280100	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533650625	chr11:71280110-71280111	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs59486429	chr11:71280120-71280121	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs114853616	chr11:71280122-71280123	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs182848826	chr11:71280129-71280130	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs375120582	chr11:71280136-71280137	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557615550	chr11:71280137-71280138	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs60034732	chr11:71280145-71280146	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536616416	chr11:71280158-71280159	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs555015772	chr11:71280160-71280161	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573330763	chr11:71280161-71280162	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs540728209	chr11:71280171-71280172	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs559134695	chr11:71280174-71280175	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576953339	chr11:71280184-71280185	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs61517798	chr11:71280188-71280189	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs562772851	chr11:71280196-71280197	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532446324	chr11:71280197-71280198	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs72256065	chr11:71280203-71280204	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187449121	chr11:71280212-71280213	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115824748	chr11:71280213-71280214	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191078344	chr11:71280218-71280219	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71277200-71280400	Enhancers	Adipose Nuclei	Adipose
2	chr11:71277400-71279800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:71277600-71279800	Weak transcription	Left Ventricle	heart
4	chr11:71277600-71280400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:71277600-71281600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:71277600-71282800	Weak transcription	Fetal Intestine Small	intestine
7	chr11:71277600-71290400	Weak transcription	Right Atrium	heart
8	chr11:71278000-71279800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr11:71278200-71281600	Weak transcription	Spleen	Spleen
10	chr11:71278400-71279800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr11:71279000-71280200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:71279000-71280600	Enhancers	Fetal Muscle Leg	muscle
13	chr11:71279000-71281200	Enhancers	Fetal Stomach	stomach
14	chr11:71279200-71280400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:71279400-71280000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr11:71279400-71281400	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr11:71279600-71280200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr11:71279600-71280200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr11:71279600-71280200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:71279600-71280200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:71279600-71280200	Enhancers	Psoas Muscle	Psoas
22	chr11:71279600-71280200	Enhancers	Stomach Smooth Muscle	stomach
23	chr11:71279600-71280200	Flanking Bivalent TSS/Enh	HepG2	liver
24	chr11:71279600-71280400	Enhancers	Fetal Lung	lung
25	chr11:71279600-71282000	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr11:71279800-71280000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr11:71279800-71280000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:71279800-71280200	Enhancers	Colon Smooth Muscle	Colon
29	chr11:71279800-71280200	Enhancers	Left Ventricle	heart
30	chr11:71279800-71280400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr11:71279800-71280400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr11:71279800-71280600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr11:71280000-71280200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr11:71280000-71280200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:71280000-71280400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr11:71280000-71281800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr11:71280200-71280400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr11:71280200-71280400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr11:71280200-71280400	Bivalent Enhancer	HepG2	liver
40	chr11:71280200-71281800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr11:71281200-71281400	Bivalent Enhancer	Fetal Stomach	stomach
42	chr11:71281400-71281800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
43	chr11:71281600-71281800	Enhancers	Spleen	Spleen
44	chr11:71281600-71282000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:71281800-71282000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr11:71281800-71282000	Enhancers	H9 Cell Line	embryonic stem cell
47	chr11:71281800-71282000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr11:71281800-71282000	Bivalent Enhancer	Fetal Kidney	kidney
49	chr11:71282000-71282200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr11:71282000-71285000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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