Variant report

Variant	nsv1054575
Chromosome Location	chr11:71352127-71536860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3184)
CpG islands
(count:2076)
Chromatin interactive
region (count:10)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3184 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
2	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
3	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
4	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
6	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
7	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
8	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
9	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
10	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
11	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
12	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
13	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
14	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
15	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
16	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
17	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
18	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
20	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
21	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
23	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
24	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
25	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
26	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
27	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
28	BATF	chr11:71376144-71376697	GM12878	blood:	n/a	n/a
29	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
30	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
31	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
32	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
33	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
34	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
35	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
36	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
37	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890
38	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
39	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
40	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
41	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
42	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
43	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
44	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
45	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
46	BATF	chr11:71532357-71532883	GM12878	blood:	n/a	n/a
47	BATF	chr11:71364018-71364247	GM12878	blood:	n/a	chr11:71364110-71364121
48	BATF	chr11:71364307-71364538	GM12878	blood:	n/a	n/a
49	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
50	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a

(count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71417713-71417763	BJ	skin:	n/a
2	chr11:71493933-71493983	HNPCEpiC	eye:	n/a
3	chr11:71417713-71417763	BJ	skin:	n/a
4	chr11:71493933-71493983	HNPCEpiC	eye:	n/a
5	chr11:71352122-71352172	GM19239	blood:	n/a
6	chr11:71499117-71499167	HL-60	blood:	n/a
7	chr11:71456947-71456997	ovcar-3	ovarian:	n/a
8	chr11:71497688-71497738	HRE	kidney:	n/a
9	chr11:71524540-71524590	MCF10A-Er-Src	breast:	n/a
10	chr11:71498202-71498252	GM12892	blood:	n/a
11	chr11:71353991-71354041	NHDF-neo	bronchial:	n/a
12	chr11:71499006-71499056	GM12878	blood:	n/a
13	chr11:71352122-71352172	IMR90	lung:	fetal
14	chr11:71522461-71522511	U87	brain:	n/a
15	chr11:71499006-71499056	NB4	blood:	n/a
16	chr11:71421380-71421430	Hela-S3	cervix:	n/a
17	chr11:71456947-71456997	AG10803	skin:	n/a
18	chr11:71352122-71352172	GM06990	blood:	n/a
19	chr11:71524971-71525021	GM19239	blood:	n/a
20	chr11:71527895-71527945	NH-A	brain:	n/a
21	chr11:71511486-71511536	Hepatocyte	liver:	n/a
22	chr11:71524971-71525021	AoSMC	blood vessel:	n/a
23	chr11:71417657-71417707	AoSMC	blood vessel:	n/a
24	chr11:71462582-71462632	HNPCEpiC	eye:	n/a
25	chr11:71524734-71524784	SK-N-SH_RA	brain:	n/a
26	chr11:71524971-71525021	GM12878	blood:	n/a
27	chr11:71524971-71525021	NHDF-neo	bronchial:	n/a
28	chr11:71353991-71354041	SAEC	small airway:	n/a
29	chr11:71522461-71522511	Hepatocyte	liver:	n/a
30	chr11:71499117-71499167	HCM	heart:	n/a
31	chr11:71462549-71462599	SK-N-SH_RA	brain:	n/a
32	chr11:71485830-71485880	HepG2	liver:	n/a
33	chr11:71524971-71525021	MCF10A-Er-Src	breast:	n/a
34	chr11:71497552-71497602	Hepatocyte	liver:	n/a
35	chr11:71524734-71524784	HCM	heart:	n/a
36	chr11:71420485-71420535	IMR90	lung:	fetal
37	chr11:71522461-71522511	MCF10A-Er-Src	breast:	n/a
38	chr11:71420947-71420997	ProgFib	skin:	n/a
39	chr11:71456947-71456997	Hela-S3	cervix:	n/a
40	chr11:71498609-71498659	AG04449	skin:	fetal
41	chr11:71352122-71352172	HCM	heart:	n/a
42	chr11:71457160-71457210	SAEC	small airway:	n/a
43	chr11:71499006-71499056	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:71457160-71457210	HIPEpiC	eye:	n/a
45	chr11:71497688-71497738	BE2_C	brain:	n/a
46	chr11:71498715-71498765	U87	brain:	n/a
47	chr11:71524971-71525021	HCM	heart:	n/a
48	chr11:71420485-71420535	Jurkat	blood:	n/a
49	chr11:71418204-71418254	AG04449	skin:	fetal
50	chr11:71499006-71499056	HCF	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:3442224..3443750-chr11:71497854..71499382,2	MCF-7	breast:
2	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
3	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
4	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
5	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
6	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
7	chr11:71498143..71498944-chr16:5147397..5148064,2	Hela-S3	cervix:
8	chr11:71489714..71493464-chr11:71497648..71499552,3	MCF-7	breast:
9	chr11:71502585..71504558-chr11:71523085..71525009,2	MCF-7	breast:
10	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
2	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3
3	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
4	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
5	lnc-RP11-849H4.2.1-1	chr11:71527956-71528142	ENSG00000248671.3
6	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
7	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
8	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
9	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713
10	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
11	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+
12	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
13	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
14	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
15	lnc-AP000867.1-2	chr11:71383721-71384047	ENSG00000254504.1
16	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
17	lnc-RP11-849H4.2.1-1	chr11:71529199-71529284	ENSG00000248671.3
18	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701

No data

Variant related genes	Relation type
FAM86C1	TF binding region
ENSG00000248671	TF binding region
ZNF705E	TF binding region
ENSG00000223235	TF binding region
ENSG00000264091	TF binding region
ENSG00000254805	TF binding region
ALG1L9P	TF binding region
ENPP7P8	TF binding region
ENSG00000254972	TF binding region
ENSG00000221458	TF binding region
RPS3AP41	TF binding region
FAM86C1	CpG island
ENSG00000248671	CpG island
ZNF705E	CpG island
ENSG00000223235	CpG island
ENSG00000264091	CpG island
ENSG00000254805	CpG island
ALG1L9P	CpG island
ENPP7P8	CpG island
ENSG00000254972	CpG island
ENSG00000221458	CpG island
RPS3AP41	CpG island
ENSG00000160172	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000244026	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000118894	chromatin interactions

Extended variants
information (count: 9611 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:9611 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577782705	chr11:71352142-71352143	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs193282234	chr11:71352159-71352160	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144619129	chr11:71352169-71352170	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575847114	chr11:71352186-71352187	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543342849	chr11:71352199-71352200	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531112509	chr11:71352202-71352203	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139013278	chr11:71352225-71352226	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373825415	chr11:71352226-71352227	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547085406	chr11:71352229-71352230	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116555735	chr11:71352233-71352234	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142287733	chr11:71352245-71352246	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550552019	chr11:71352288-71352289	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184602091	chr11:71352303-71352304	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7395840	chr11:71352315-71352316	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs569223347	chr11:71352326-71352327	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536116596	chr11:71352364-71352365	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146394654	chr11:71352382-71352383	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566104629	chr11:71352414-71352415	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370405002	chr11:71352417-71352418	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539856513	chr11:71352422-71352423	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374573635	chr11:71352423-71352424	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139344562	chr11:71352472-71352473	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576510715	chr11:71352492-71352493	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537995050	chr11:71352498-71352499	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191131297	chr11:71352540-71352541	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575802205	chr11:71352550-71352551	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542902420	chr11:71352552-71352553	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551832983	chr11:71352599-71352600	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4945101	chr11:71352608-71352609	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370758413	chr11:71352640-71352641	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184004475	chr11:71352649-71352650	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540614951	chr11:71352650-71352651	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190041746	chr11:71352651-71352652	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56033693	chr11:71352667-71352668	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532648893	chr11:71352693-71352694	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551095363	chr11:71352696-71352697	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562498290	chr11:71352716-71352717	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112225655	chr11:71352738-71352739	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529920386	chr11:71352763-71352764	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181233129	chr11:71352764-71352765	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4945102	chr11:71352767-71352768	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs78740078	chr11:71352807-71352808	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533861150	chr11:71352808-71352809	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551749804	chr11:71352819-71352820	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570150998	chr11:71352824-71352825	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372161720	chr11:71352840-71352841	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4945103	chr11:71352881-71352882	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs151227086	chr11:71352943-71352944	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200747156	chr11:71352994-71352995	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201367915	chr11:71353014-71353015	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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 cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71350800-71354400	Weak transcription	Esophagus	oesophagus
2	chr11:71351200-71353400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:71351800-71352200	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:71352000-71352200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
5	chr11:71352000-71352200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
6	chr11:71352000-71352200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:71352000-71357600	Weak transcription	Fetal Intestine Large	intestine
8	chr11:71352000-71357800	Weak transcription	Fetal Intestine Small	intestine
9	chr11:71352200-71352400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr11:71353400-71359800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:71353800-71354000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr11:71354000-71366400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr11:71357600-71359400	Enhancers	Fetal Intestine Large	intestine
14	chr11:71357800-71359800	Enhancers	Fetal Intestine Small	intestine
15	chr11:71358400-71360000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr11:71358800-71360000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:71359000-71359600	Enhancers	Primary hematopoietic stem cells	blood
18	chr11:71359000-71360400	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr11:71359200-71360200	Enhancers	Stomach Mucosa	stomach
20	chr11:71359600-71360400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr11:71359800-71360000	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr11:71359800-71360400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:71359800-71367600	Weak transcription	Fetal Intestine Small	intestine
24	chr11:71360000-71360200	Enhancers	Lung	lung
25	chr11:71360400-71362000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr11:71360400-71373000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:71362200-71362400	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr11:71362400-71362800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr11:71363600-71364600	Enhancers	GM12878-XiMat	blood
30	chr11:71366400-71366800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr11:71366400-71367800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr11:71367200-71367400	Enhancers	Fetal Intestine Large	intestine
33	chr11:71367200-71367800	Enhancers	A549	lung
34	chr11:71367400-71367600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr11:71367600-71368000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr11:71367600-71368200	Enhancers	Fetal Intestine Small	intestine
37	chr11:71368000-71368200	Enhancers	Fetal Intestine Large	intestine
38	chr11:71368200-71395600	Weak transcription	Fetal Intestine Small	intestine
39	chr11:71385800-71386000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr11:71394000-71396800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:71395600-71396200	Enhancers	Fetal Intestine Large	intestine
42	chr11:71395600-71396200	Enhancers	Fetal Intestine Small	intestine
43	chr11:71396200-71396400	Weak transcription	Fetal Intestine Large	intestine
44	chr11:71396200-71398000	Active TSS	Fetal Intestine Small	intestine
45	chr11:71396400-71398000	Active TSS	Fetal Intestine Large	intestine
46	chr11:71396800-71404000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:71400200-71400600	Enhancers	K562	blood
48	chr11:71400600-71403400	Weak transcription	K562	blood
49	chr11:71403400-71403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr11:71403400-71404400	Enhancers	K562	blood

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