Variant report

Variant	nsv897899
Chromosome Location	chr11:71234107-71277981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:672)
CpG islands
(count:1648)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71246189-71246536	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:71237205-71237575	HepG2	liver:	n/a	n/a
3	ATF1	chr11:71274374-71274763	K562	blood:	n/a	n/a
4	ATF2	chr11:71254369-71254678	GM12878	blood:	n/a	n/a
5	ATF2	chr11:71251016-71252199	GM12878	blood:	n/a	n/a
6	ATF2	chr11:71251026-71251407	GM12878	blood:	n/a	n/a
7	ATF2	chr11:71241553-71242059	GM12878	blood:	n/a	n/a
8	ATF2	chr11:71262610-71263131	GM12878	blood:	n/a	n/a
9	ATF2	chr11:71254252-71254755	GM12878	blood:	n/a	n/a
10	ATF2	chr11:71251483-71252131	GM12878	blood:	n/a	n/a
11	BACH1	chr11:71262748-71263014	K562	blood:	n/a	n/a
12	BACH1	chr11:71262761-71263011	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr11:71262740-71263045	GM12878	blood:	n/a	chr11:71262880-71262891
14	BATF	chr11:71251533-71252059	GM12878	blood:	n/a	n/a
15	BATF	chr11:71251039-71251366	GM12878	blood:	n/a	n/a
16	BATF	chr11:71254310-71254769	GM12878	blood:	n/a	n/a
17	BATF	chr11:71262648-71263064	GM12878	blood:	n/a	chr11:71262880-71262891
18	BATF	chr11:71254317-71254656	GM12878	blood:	n/a	n/a
19	BATF	chr11:71250991-71251419	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:71241675-71242012	GM12878	blood:	n/a	n/a
21	BCL3	chr11:71267088-71267530	GM12878	blood:	n/a	n/a
22	BCL3	chr11:71251547-71252137	GM12878	blood:	n/a	n/a
23	BCLAF1	chr11:71241632-71241998	GM12878	blood:	n/a	n/a
24	BCLAF1	chr11:71251487-71252042	GM12878	blood:	n/a	n/a
25	BCLAF1	chr11:71251510-71252067	GM12878	blood:	n/a	n/a
26	BCLAF1	chr11:71250921-71251422	GM12878	blood:	n/a	chr11:71251210-71251219
27	BHLHE40	chr11:71246155-71246217	K562	blood:	n/a	n/a
28	BHLHE40	chr11:71242536-71242718	K562	blood:	n/a	n/a
29	BHLHE40	chr11:71274540-71274790	GM12878	blood:	n/a	n/a
30	BHLHE40	chr11:71251215-71251234	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:71251666-71251812	GM12878	blood:	n/a	n/a
32	BHLHE40	chr11:71254944-71255240	GM12878	blood:	n/a	n/a
33	BRCA1	chr11:71274467-71274725	HepG2	liver:	n/a	n/a
34	CEBPB	chr11:71242999-71243345	K562	blood:	n/a	chr11:71243155-71243166
35	CEBPB	chr11:71267943-71268156	IMR90	lung:	n/a	n/a
36	CEBPB	chr11:71237228-71237488	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:71246443-71246484	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:71243021-71243338	K562	blood:	n/a	chr11:71243155-71243166
39	CEBPB	chr11:71243045-71243245	IMR90	lung:	n/a	chr11:71243155-71243166
40	CEBPB	chr11:71264971-71265142	K562	blood:	n/a	n/a
41	CEBPB	chr11:71243014-71243347	HepG2	liver:	n/a	chr11:71243155-71243166
42	CEBPD	chr11:71245996-71246415	K562	blood:	n/a	n/a
43	CHD2	chr11:71239563-71239592	HepG2	liver:	n/a	n/a
44	CHD2	chr11:71274596-71274796	HepG2	liver:	n/a	n/a
45	CHD2	chr11:71252046-71252130	K562	blood:	n/a	n/a
46	CREB1	chr11:71241508-71242063	GM12878	blood:	n/a	n/a
47	CREB1	chr11:71241529-71242085	GM12878	blood:	n/a	n/a
48	CTCF	chr11:71240881-71241001	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr11:71240906-71240912	GM19238	blood:	n/a	n/a
50	CTCF	chr11:71274640-71274790	HA-sp	spinal cord:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71239055-71239105	AG09309	skin:	n/a
2	chr11:71239055-71239105	AG09309	skin:	n/a
3	chr11:71235111-71235161	T-47D	breast:	n/a
4	chr11:71248741-71248791	H1-hESC	embryonic stem cell:	embryo
5	chr11:71259439-71259489	PFSK-1	brain:	n/a
6	chr11:71248906-71248956	HRCEpiC	kidney:	n/a
7	chr11:71235111-71235161	A549	lung:	n/a
8	chr11:71237650-71237700	U87	brain:	n/a
9	chr11:71238382-71238432	GM19239	blood:	n/a
10	chr11:71237522-71237572	PFSK-1	brain:	n/a
11	chr11:71259439-71259489	AG04449	skin:	fetal
12	chr11:71249212-71249262	SKMC	muscle:	n/a
13	chr11:71238270-71238320	HL-60	blood:	n/a
14	chr11:71275784-71275834	HMEC	breast:	n/a
15	chr11:71248906-71248956	SK-N-SH	brain:	n/a
16	chr11:71237650-71237700	BE2_C	brain:	n/a
17	chr11:71259341-71259391	PFSK-1	brain:	n/a
18	chr11:71275784-71275834	AG10803	skin:	n/a
19	chr11:71276557-71276607	HMEC	breast:	n/a
20	chr11:71258392-71258442	AoSMC	blood vessel:	n/a
21	chr11:71258392-71258442	AG10803	skin:	n/a
22	chr11:71239055-71239105	HEK293	kidney:	embryo
23	chr11:71259292-71259342	GM19239	blood:	n/a
24	chr11:71275784-71275834	Caco-2	colon:	n/a
25	chr11:71249212-71249262	HRPEpiC	eye:	n/a
26	chr11:71277473-71277523	BJ	skin:	n/a
27	chr11:71250073-71250123	HRCEpiC	kidney:	n/a
28	chr11:71248741-71248791	GM12878	blood:	n/a
29	chr11:71238382-71238432	Hepatocyte	liver:	n/a
30	chr11:71239055-71239105	H1-hESC	embryonic stem cell:	embryo
31	chr11:71258392-71258442	NHDF-neo	bronchial:	n/a
32	chr11:71258392-71258442	ovcar-3	ovarian:	n/a
33	chr11:71237522-71237572	HPAEpiC	pulmonary alveolar:	n/a
34	chr11:71237522-71237572	GM12892	blood:	n/a
35	chr11:71259341-71259391	HRE	kidney:	n/a
36	chr11:71238270-71238320	SK-N-SH_RA	brain:	n/a
37	chr11:71250073-71250123	RPTEC	kidney:	n/a
38	chr11:71259439-71259489	GM12891	blood:	n/a
39	chr11:71248448-71248498	SK-N-SH	brain:	n/a
40	chr11:71238382-71238432	AG04449	skin:	fetal
41	chr11:71248906-71248956	HCT-116	colon:	n/a
42	chr11:71249212-71249262	A549	lung:	n/a
43	chr11:71258392-71258442	HCT-116	colon:	n/a
44	chr11:71238225-71238275	T-47D	breast:	n/a
45	chr11:71248448-71248498	HRPEpiC	eye:	n/a
46	chr11:71259341-71259391	AG04450	lung:	fetal
47	chr11:71276557-71276607	Hepatocyte	liver:	n/a
48	chr11:71249212-71249262	SK-N-SH_RA	brain:	n/a
49	chr11:71259341-71259391	Hela-S3	cervix:	n/a
50	chr11:71276557-71276607	ProgFib	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71257442..71259140-chr11:71259571..71262525,2	K562	blood:
2	chr11:71176264..71179140-chr11:71273245..71275842,2	MCF-7	breast:
3	chr11:71198148..71200436-chr11:71273726..71275977,2	MCF-7	breast:
4	chr11:71159116..71165503-chr11:71274687..71279227,9	MCF-7	breast:
5	chr11:71257442..71259140-chr11:71259571..71262525,2	K562	blood:
6	chr11:71156732..71161621-chr11:71272936..71276184,4	MCF-7	breast:
7	chr11:71253515..71257343-chr11:71260479..71262893,3	MCF-7	breast:
8	chr11:71254168..71255682-chr11:71257713..71259935,2	MCF-7	breast:
9	chr11:71253515..71257343-chr11:71260479..71262893,3	MCF-7	breast:
10	chr11:71209230..71212129-chr11:71251545..71253303,2	MCF-7	breast:
11	chr11:71272055..71274887-chr11:71280546..71282110,2	K562	blood:
12	chr11:71189071..71191550-chr11:71272066..71273804,2	MCF-7	breast:

No data

Variant related genes	Relation type
KRTAP5-10	TF binding region
KRTAP5-7	TF binding region
KRTAP5-9	TF binding region
ENSG00000248903	TF binding region
KRTAP5-8	TF binding region
KRTAP5-10	CpG island
KRTAP5-7	CpG island
KRTAP5-9	CpG island
ENSG00000248903	CpG island
KRTAP5-8	CpG island
ENSG00000172893	chromatin interactions
ENSG00000254997	chromatin interactions
ENSG00000172890	chromatin interactions
ENSG00000254682	chromatin interactions

Extended variants
information (count: 2021 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2021 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11234027	chr11:71234107-71234108	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369347453	chr11:71234132-71234133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117444721	chr11:71234133-71234134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs28481909	chr11:71234146-71234147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566335957	chr11:71234206-71234207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540051064	chr11:71234209-71234210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183385528	chr11:71234210-71234211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199987525	chr11:71234221-71234222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576229302	chr11:71234237-71234238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202013496	chr11:71234245-71234246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375831159	chr11:71234254-71234255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs28468070	chr11:71234324-71234325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573561717	chr11:71234362-71234363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536493622	chr11:71234385-71234386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545128841	chr11:71234400-71234401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142380094	chr11:71234426-71234427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs80243360	chr11:71234474-71234475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151310281	chr11:71234525-71234526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75819606	chr11:71234531-71234532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186270124	chr11:71234548-71234549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140495926	chr11:71234582-71234583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550003583	chr11:71234597-71234598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190643891	chr11:71234615-71234616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541333065	chr11:71234654-71234655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553834445	chr11:71234716-71234717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547734687	chr11:71234728-71234729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183251419	chr11:71234800-71234801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540499461	chr11:71234828-71234829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540114188	chr11:71234954-71234955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555554276	chr11:71234970-71234971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558420881	chr11:71235023-71235024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570251837	chr11:71235095-71235096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577178476	chr11:71235112-71235113	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs537608150	chr11:71235121-71235122	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs555182606	chr11:71235127-71235128	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs370258082	chr11:71235154-71235155	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs2155420	chr11:71235177-71235178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2186773	chr11:71235194-71235195	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111676332	chr11:71235299-71235300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2096801	chr11:71235314-71235315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192215163	chr11:71235357-71235358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2096800	chr11:71235374-71235375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150436017	chr11:71235414-71235415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182962428	chr11:71235446-71235447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531872236	chr11:71235448-71235449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187930575	chr11:71235509-71235510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192997968	chr11:71235547-71235548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138134855	chr11:71235564-71235565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184329243	chr11:71235582-71235583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529358155	chr11:71235599-71235600	Weak transcription	n/a	n/a	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
Breast cancer	21785460	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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71215600-71236600	Weak transcription	Brain Anterior Caudate	brain
2	chr11:71216400-71235400	Weak transcription	Brain Substantia Nigra	brain
3	chr11:71230400-71235800	Weak transcription	Brain Hippocampus Middle	brain
4	chr11:71232800-71236400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr11:71232800-71236600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr11:71232800-71243600	Weak transcription	Brain Angular Gyrus	brain
7	chr11:71232800-71245800	Weak transcription	Pancreas	Pancrea
8	chr11:71232800-71259800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr11:71233000-71235600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr11:71235800-71238000	Enhancers	HepG2	liver
11	chr11:71236200-71239200	Enhancers	Liver	Liver
12	chr11:71236400-71237800	Enhancers	A549	lung
13	chr11:71236600-71236800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
14	chr11:71236600-71237400	Enhancers	Stomach Mucosa	stomach
15	chr11:71236800-71237000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr11:71237200-71238800	Enhancers	Fetal Intestine Large	intestine
17	chr11:71237400-71238200	Enhancers	Fetal Intestine Small	intestine
18	chr11:71238000-71238200	Flanking Active TSS	HepG2	liver
19	chr11:71238200-71238600	Active TSS	HepG2	liver
20	chr11:71238600-71239000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr11:71238600-71239000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr11:71238600-71239000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr11:71238600-71239200	Flanking Active TSS	HepG2	liver
24	chr11:71239000-71241400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr11:71239000-71246400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr11:71239200-71239800	Enhancers	HepG2	liver
27	chr11:71239800-71241600	Weak transcription	HepG2	liver
28	chr11:71241400-71242600	Enhancers	GM12878-XiMat	blood
29	chr11:71241400-71244400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr11:71241600-71242600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr11:71241600-71243400	Enhancers	HepG2	liver
32	chr11:71241800-71243600	Enhancers	K562	blood
33	chr11:71243400-71244000	Weak transcription	HepG2	liver
34	chr11:71243600-71244000	Weak transcription	K562	blood
35	chr11:71244000-71245800	Enhancers	HepG2	liver
36	chr11:71244000-71247200	Enhancers	K562	blood
37	chr11:71244400-71245200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:71245200-71247200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr11:71245400-71246800	Enhancers	Fetal Intestine Large	intestine
40	chr11:71245400-71247200	Enhancers	Fetal Intestine Small	intestine
41	chr11:71245400-71247400	Enhancers	Liver	Liver
42	chr11:71245800-71246400	Flanking Active TSS	HepG2	liver
43	chr11:71245800-71246600	Enhancers	Pancreas	Pancrea
44	chr11:71245800-71246800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr11:71246000-71246200	Enhancers	GM12878-XiMat	blood
46	chr11:71246200-71246600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr11:71246200-71247000	Weak transcription	GM12878-XiMat	blood
48	chr11:71246400-71246800	Active TSS	HepG2	liver
49	chr11:71246800-71247000	Flanking Active TSS	HepG2	liver
50	chr11:71246800-71247800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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