Variant report

Variant	nsv555405
Chromosome Location	chr11:71944667-71952345
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:746)
CpG islands
(count:552)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:71949146-71949549	GM12878	blood:	n/a	n/a
2	ATF2	chr11:71950345-71950869	GM12878	blood:	n/a	n/a
3	ATF2	chr11:71948937-71949664	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr11:71949019-71949601	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr11:71949208-71949529	K562	blood:	n/a	n/a
6	BACH1	chr11:71951991-71952347	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:71949157-71949418	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr11:71950226-71950969	A549	lung:	n/a	n/a
9	BCL3	chr11:71949402-71950016	A549	lung:	n/a	n/a
10	BCL3	chr11:71950436-71951227	GM12878	blood:	n/a	n/a
11	BCL3	chr11:71950862-71951168	GM12878	blood:	n/a	n/a
12	BCL3	chr11:71950550-71950854	GM12878	blood:	n/a	n/a
13	BCL3	chr11:71950198-71950904	A549	lung:	n/a	n/a
14	BCL3	chr11:71949148-71949594	A549	lung:	n/a	chr11:71949241-71949250 chr11:71949277-71949286
15	BHLHE40	chr11:71952174-71952190	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:71949252-71949460	K562	blood:	n/a	n/a
17	BRCA1	chr11:71949019-71949496	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr11:71949147-71949669	K562	blood:	n/a	n/a
19	CCNT2	chr11:71949044-71949516	K562	blood:	n/a	chr11:71949222-71949231
20	CCNT2	chr11:71950517-71951216	K562	blood:	n/a	n/a
21	CEBPB	chr11:71949260-71949450	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:71949231-71949488	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr11:71950540-71950738	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr11:71950536-71951267	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr11:71949084-71949546	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr11:71949068-71949544	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr11:71949212-71949524	K562	blood:	n/a	n/a
28	CHD2	chr11:71951044-71951378	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr11:71949345-71949395	HepG2	liver:	n/a	n/a
30	CREB1	chr11:71949009-71949571	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr11:71949215-71949459	A549	lung:	n/a	n/a
32	CREB1	chr11:71949044-71949652	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr11:71949111-71949623	A549	lung:	n/a	n/a
34	CTCF	chr11:71948300-71948450	HFF	foreskin:	n/a	n/a
35	CTCF	chr11:71948180-71948330	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr11:71949300-71949450	AG10803	skin:	n/a	n/a
37	CTCF	chr11:71949300-71949450	NHEK	skin:	n/a	n/a
38	CTCF	chr11:71949300-71949450	HCFaa	heart:	n/a	n/a
39	CTCF	chr11:71949247-71949469	ECC-1	luminal epithelium:	n/a	n/a
40	CTCF	chr11:71948080-71948230	K562	blood:	n/a	n/a
41	CTCF	chr11:71948140-71948290	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr11:71949280-71949430	GM12865	blood:	n/a	n/a
43	CTCF	chr11:71949280-71949430	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr11:71949234-71949514	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr11:71949340-71949490	HCM	heart:	n/a	n/a
46	CTCF	chr11:71949177-71949188	GM12891	blood:	n/a	n/a
47	CTCF	chr11:71951760-71951910	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr11:71949945-71950038	GM12892	blood:	n/a	n/a
49	CTCF	chr11:71948130-71948179	GM20000	blood:	n/a	n/a
50	CTCF	chr11:71948080-71948230	AG04449	skin:	n/a	n/a

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71950053-71950103	AG10803	skin:	n/a
2	chr11:71951279-71951329	LNCaP	prostate:	n/a
3	chr11:71950660-71950710	NHBE	bronchial:	n/a
4	chr11:71950053-71950103	AG10803	skin:	n/a
5	chr11:71951279-71951329	LNCaP	prostate:	n/a
6	chr11:71950660-71950710	NHBE	bronchial:	n/a
7	chr11:71952131-71952181	NHDF-neo	bronchial:	n/a
8	chr11:71950660-71950710	A549	lung:	n/a
9	chr11:71950053-71950103	HUVEC	blood vessel:	n/a
10	chr11:71951122-71951172	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:71952131-71952181	NHBE	bronchial:	n/a
12	chr11:71950053-71950103	T-47D	breast:	n/a
13	chr11:71950053-71950103	A549	lung:	n/a
14	chr11:71950053-71950103	PFSK-1	brain:	n/a
15	chr11:71952131-71952181	GM12892	blood:	n/a
16	chr11:71950053-71950103	HepG2	liver:	n/a
17	chr11:71950924-71950974	AG04449	skin:	fetal
18	chr11:71951122-71951172	AG04449	skin:	fetal
19	chr11:71948712-71948762	HEEpiC	esophagus:	n/a
20	chr11:71951122-71951172	ProgFib	skin:	n/a
21	chr11:71951279-71951329	PANC-1	pancreas:	n/a
22	chr11:71951714-71951764	HRE	kidney:	n/a
23	chr11:71950660-71950710	HCT-116	colon:	n/a
24	chr11:71950053-71950103	HL-60	blood:	n/a
25	chr11:71950660-71950710	Jurkat	blood:	n/a
26	chr11:71950924-71950974	Hepatocyte	liver:	n/a
27	chr11:71952131-71952181	HMEC	breast:	n/a
28	chr11:71946371-71946421	IMR90	lung:	fetal
29	chr11:71950053-71950103	U87	brain:	n/a
30	chr11:71950924-71950974	PANC-1	pancreas:	n/a
31	chr11:71951279-71951329	HIPEpiC	eye:	n/a
32	chr11:71951122-71951172	HRE	kidney:	n/a
33	chr11:71950924-71950974	PFSK-1	brain:	n/a
34	chr11:71946371-71946421	HRCEpiC	kidney:	n/a
35	chr11:71946371-71946421	HAEpiC	amniotic membrane:	n/a
36	chr11:71950053-71950103	MCF-7	breast:	n/a
37	chr11:71951122-71951172	RPTEC	kidney:	n/a
38	chr11:71946371-71946421	U87	brain:	n/a
39	chr11:71952131-71952181	NH-A	brain:	n/a
40	chr11:71946371-71946421	CMK	blood:	n/a
41	chr11:71952131-71952181	CMK	blood:	n/a
42	chr11:71950660-71950710	ovcar-3	ovarian:	n/a
43	chr11:71951714-71951764	SAEC	small airway:	n/a
44	chr11:71952131-71952181	LNCaP	prostate:	n/a
45	chr11:71951714-71951764	SK-N-MC	brain:	n/a
46	chr11:71951122-71951172	IMR90	lung:	fetal
47	chr11:71951122-71951172	ovcar-3	ovarian:	n/a
48	chr11:71946371-71946421	HEK293	kidney:	embryo
49	chr11:71952131-71952181	HCPEpiC	choroid plexus:	n/a
50	chr11:71948712-71948762	Hela-S3	cervix:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71948375..71952014-chr11:71952052..71958381,8	MCF-7	breast:
2	chr11:71734617..71736774-chr11:71947539..71949807,2	MCF-7	breast:
3	chr11:71894266..71895107-chr11:71949011..71949837,3	MCF-7	breast:
4	chr11:71949479..71951633-chr11:72139393..72142208,2	K562	blood:
5	chr11:71951601..71953593-chr11:71954198..71956638,2	K562	blood:
6	chr11:71812888..71815663-chr11:71949421..71951331,2	MCF-7	breast:
7	chr11:71948861..71949664-chr11:72144832..72145336,2	MCF-7	breast:
8	chr11:71815942..71818522-chr11:71943866..71946809,2	K562	blood:
9	chr11:71948375..71952014-chr11:71952052..71958381,8	MCF-7	breast:
10	chr11:71713190..71714745-chr11:71948791..71950410,2	K562	blood:
11	chr11:71723194..71726024-chr11:71949814..71951680,2	K562	blood:
12	chr11:71950675..71951425-chr12:120729547..120730055,2	Hela-S3	cervix:
13	chr11:71736273..71736838-chr11:71948885..71950174,5	K562	blood:
14	chr11:71948874..71949407-chr11:72144827..72145714,3	K562	blood:
15	chr11:71944736..71947658-chr11:71947860..71951396,7	K562	blood:
16	chr11:71810891..71813222-chr11:71944678..71946447,2	MCF-7	breast:
17	chr11:71822963..71824981-chr11:71949478..71951249,2	K562	blood:
18	chr11:71821211..71823051-chr11:71942558..71945428,2	K562	blood:
19	chr11:71822074..71824400-chr11:71947784..71949539,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	INPPL1	hsa-miR-205-5p	chr11:71949830-71949849
2	INPPL1	hsa-miR-205-5p	chr11:71949842-71949849
3	INPPL1	hsa-miR-184	chr11:71949831-71949837

Variant related genes	Relation type
INPPL1	TF binding region
PHOX2A	TF binding region
INPPL1	CpG island
PHOX2A	CpG island
ENSG00000202538	chromatin interactions
ENSG00000165458	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000184154	chromatin interactions
ENSG00000165462	chromatin interactions
ENSG00000137497	chromatin interactions
ENSG00000251143	chromatin interactions
ENSG00000238768	chromatin interactions
ENSG00000110200	chromatin interactions
ENSG00000162129	chromatin interactions

Extended variants
information (count: 322 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1006488	chr11:71944667-71944668	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151248494	chr11:71944684-71944685	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs145978702	chr11:71944724-71944725	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs139798970	chr11:71944736-71944737	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs116848359	chr11:71944737-71944738	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs397514512	chr11:71944740-71944741	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs35524893	chr11:71944767-71944768	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs141544846	chr11:71944775-71944776	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs370132708	chr11:71944814-71944815	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs374684737	chr11:71944828-71944829	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs190979516	chr11:71944834-71944835	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs183127059	chr11:71944850-71944851	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs188213012	chr11:71944863-71944864	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs538260033	chr11:71944874-71944875	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs547977606	chr11:71945009-71945010	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs574790730	chr11:71945010-71945011	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs559999694	chr11:71945025-71945026	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs140470303	chr11:71945042-71945043	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs182717109	chr11:71945056-71945057	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs150400009	chr11:71945063-71945064	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs374083827	chr11:71945098-71945099	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs570204792	chr11:71945116-71945117	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs554258474	chr11:71945140-71945141	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs79023399	chr11:71945145-71945146	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs549386968	chr11:71945171-71945172	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs199936814	chr11:71945287-71945288	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs374105274	chr11:71945291-71945292	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs377672050	chr11:71945319-71945320	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs371183739	chr11:71945326-71945327	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs373473641	chr11:71945327-71945328	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs370210488	chr11:71945329-71945330	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs61736312	chr11:71945332-71945333	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs139988373	chr11:71945367-71945368	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs374511786	chr11:71945397-71945398	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs149863494	chr11:71945409-71945410	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs370540380	chr11:71945447-71945448	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs374222226	chr11:71945462-71945463	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs138958741	chr11:71945514-71945515	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs368398054	chr11:71945530-71945531	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs372121385	chr11:71945542-71945543	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs202010794	chr11:71945559-71945560	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs375879606	chr11:71945561-71945562	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs61731648	chr11:71945574-71945575	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs368970014	chr11:71945575-71945576	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs371374978	chr11:71945641-71945642	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs144781166	chr11:71945645-71945646	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs538489867	chr11:71945651-71945652	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs375941017	chr11:71945654-71945655	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs148568665	chr11:71945658-71945659	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs655423	chr11:71945660-71945661	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71937000-71949200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:71937000-71950200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr11:71937000-71950600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr11:71937000-71950600	Weak transcription	Psoas Muscle	Psoas
5	chr11:71937400-71949600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:71937400-71950000	Strong transcription	NHLF	lung
7	chr11:71937600-71949000	Weak transcription	Right Atrium	heart
8	chr11:71937600-71949400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:71937800-71946400	Strong transcription	K562	blood
10	chr11:71937800-71947400	Strong transcription	Fetal Lung	lung
11	chr11:71937800-71948400	Strong transcription	Fetal Intestine Large	intestine
12	chr11:71937800-71948800	Strong transcription	Aorta	Aorta
13	chr11:71937800-71948800	Strong transcription	Spleen	Spleen
14	chr11:71937800-71949400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:71937800-71949400	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr11:71937800-71949400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr11:71937800-71950000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr11:71938000-71948600	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr11:71938000-71949200	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr11:71938200-71945200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr11:71938200-71948200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr11:71938200-71948800	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr11:71938200-71949600	Strong transcription	Liver	Liver
24	chr11:71938200-71949600	Strong transcription	Dnd41	blood
25	chr11:71938400-71947000	Strong transcription	Pancreas	Pancrea
26	chr11:71938400-71948000	Strong transcription	Colonic Mucosa	Colon
27	chr11:71938400-71950000	Strong transcription	NHEK	skin
28	chr11:71938400-71950400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr11:71938600-71948200	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr11:71938600-71948200	Strong transcription	Gastric	stomach
31	chr11:71938600-71948200	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr11:71938600-71949000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:71938600-71950000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:71938800-71945200	Strong transcription	Primary B cells from cord blood	blood
35	chr11:71938800-71946800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr11:71938800-71947800	Strong transcription	Duodenum Mucosa	Duodenum
37	chr11:71938800-71948600	Weak transcription	Fetal Brain Male	brain
38	chr11:71938800-71948800	Strong transcription	Esophagus	oesophagus
39	chr11:71938800-71949200	Strong transcription	Osteobl	bone
40	chr11:71939000-71948000	Strong transcription	Fetal Intestine Small	intestine
41	chr11:71939000-71949000	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr11:71939000-71949000	Strong transcription	Primary hematopoietic stem cells	blood
43	chr11:71939000-71949400	Strong transcription	Ovary	ovary
44	chr11:71939000-71949400	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr11:71939000-71949400	Strong transcription	Thymus	Thymus
46	chr11:71939200-71946200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr11:71939200-71946600	Strong transcription	HepG2	liver
48	chr11:71939200-71947200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:71939200-71948200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
50	chr11:71939200-71948200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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