Variant report

Variant	esv3363568
Chromosome Location	chr11:71237277-71275754
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:651)
CpG islands
(count:1283)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:651 , 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	chr11:71262610-71263131	GM12878	blood:	n/a	n/a
5	ATF2	chr11:71251483-71252131	GM12878	blood:	n/a	n/a
6	ATF2	chr11:71251016-71252199	GM12878	blood:	n/a	n/a
7	ATF2	chr11:71241553-71242059	GM12878	blood:	n/a	n/a
8	ATF2	chr11:71251026-71251407	GM12878	blood:	n/a	n/a
9	ATF2	chr11:71254252-71254755	GM12878	blood:	n/a	n/a
10	ATF2	chr11:71254369-71254678	GM12878	blood:	n/a	n/a
11	BACH1	chr11:71262761-71263011	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:71262748-71263014	K562	blood:	n/a	n/a
13	BATF	chr11:71251533-71252059	GM12878	blood:	n/a	n/a
14	BATF	chr11:71250991-71251419	GM12878	blood:	n/a	n/a
15	BATF	chr11:71254310-71254769	GM12878	blood:	n/a	n/a
16	BATF	chr11:71254317-71254656	GM12878	blood:	n/a	n/a
17	BATF	chr11:71251039-71251366	GM12878	blood:	n/a	n/a
18	BATF	chr11:71262648-71263064	GM12878	blood:	n/a	chr11:71262880-71262891
19	BATF	chr11:71262740-71263045	GM12878	blood:	n/a	chr11:71262880-71262891
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	chr11:71251487-71252042	GM12878	blood:	n/a	n/a
24	BCLAF1	chr11:71250921-71251422	GM12878	blood:	n/a	chr11:71251210-71251219
25	BCLAF1	chr11:71241632-71241998	GM12878	blood:	n/a	n/a
26	BCLAF1	chr11:71251510-71252067	GM12878	blood:	n/a	n/a
27	BHLHE40	chr11:71246155-71246217	K562	blood:	n/a	n/a
28	BHLHE40	chr11:71251215-71251234	GM12878	blood:	n/a	n/a
29	BHLHE40	chr11:71274540-71274790	GM12878	blood:	n/a	n/a
30	BHLHE40	chr11:71254944-71255240	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:71251666-71251812	GM12878	blood:	n/a	n/a
32	BHLHE40	chr11:71242536-71242718	K562	blood:	n/a	n/a
33	BRCA1	chr11:71274467-71274725	HepG2	liver:	n/a	n/a
34	CEBPB	chr11:71237228-71237488	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:71243014-71243347	HepG2	liver:	n/a	chr11:71243155-71243166
36	CEBPB	chr11:71242999-71243345	K562	blood:	n/a	chr11:71243155-71243166
37	CEBPB	chr11:71267943-71268156	IMR90	lung:	n/a	n/a
38	CEBPB	chr11:71246443-71246484	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:71264971-71265142	K562	blood:	n/a	n/a
40	CEBPB	chr11:71243045-71243245	IMR90	lung:	n/a	chr11:71243155-71243166
41	CEBPB	chr11:71243021-71243338	K562	blood:	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	chr11:71252046-71252130	K562	blood:	n/a	n/a
45	CHD2	chr11:71274596-71274796	HepG2	liver:	n/a	n/a
46	CREB1	chr11:71241529-71242085	GM12878	blood:	n/a	n/a
47	CREB1	chr11:71241508-71242063	GM12878	blood:	n/a	n/a
48	CTCF	chr11:71274625-71274857	GM12891	blood:	n/a	n/a
49	CTCF	chr11:71240914-71240945	GM19238	blood:	n/a	n/a
50	CTCF	chr11:71274660-71274810	K562	blood:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71250073-71250123	AG09309	skin:	n/a
2	chr11:71259439-71259489	HL-60	blood:	n/a
3	chr11:71250073-71250123	AG09309	skin:	n/a
4	chr11:71259439-71259489	HL-60	blood:	n/a
5	chr11:71238270-71238320	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:71259439-71259489	PANC-1	pancreas:	n/a
7	chr11:71250073-71250123	HNPCEpiC	eye:	n/a
8	chr11:71238225-71238275	ECC-1	luminal epithelium:	n/a
9	chr11:71249212-71249262	H1-hESC	embryonic stem cell:	embryo
10	chr11:71260323-71260373	MCF10A-Er-Src	breast:	n/a
11	chr11:71259251-71259301	NT2-D1	testis:	n/a
12	chr11:71238270-71238320	NB4	blood:	n/a
13	chr11:71249212-71249262	AG09309	skin:	n/a
14	chr11:71259581-71259631	GM12891	blood:	n/a
15	chr11:71258392-71258442	Caco-2	colon:	n/a
16	chr11:71237522-71237572	AoSMC	blood vessel:	n/a
17	chr11:71248906-71248956	NH-A	brain:	n/a
18	chr11:71248448-71248498	Caco-2	colon:	n/a
19	chr11:71258392-71258442	AG10803	skin:	n/a
20	chr11:71247746-71247796	SK-N-MC	brain:	n/a
21	chr11:71260323-71260373	HRCEpiC	kidney:	n/a
22	chr11:71259581-71259631	HUVEC	blood vessel:	n/a
23	chr11:71259581-71259631	HepG2	liver:	n/a
24	chr11:71259341-71259391	SK-N-SH	brain:	n/a
25	chr11:71238382-71238432	GM12878	blood:	n/a
26	chr11:71239055-71239105	SKMC	muscle:	n/a
27	chr11:71248741-71248791	AG09319	gingival:	n/a
28	chr11:71259251-71259301	PANC-1	pancreas:	n/a
29	chr11:71238270-71238320	Hela-S3	cervix:	n/a
30	chr11:71259292-71259342	PrEC	prostate:	n/a
31	chr11:71259439-71259489	T-47D	breast:	n/a
32	chr11:71238382-71238432	SK-N-SH_RA	brain:	n/a
33	chr11:71259341-71259391	AG10803	skin:	n/a
34	chr11:71238382-71238432	RPTEC	kidney:	n/a
35	chr11:71259439-71259489	HUVEC	blood vessel:	n/a
36	chr11:71238382-71238432	ECC-1	luminal epithelium:	n/a
37	chr11:71248906-71248956	IMR90	lung:	fetal
38	chr11:71258392-71258442	HMEC	breast:	n/a
39	chr11:71238270-71238320	HEK293	kidney:	embryo
40	chr11:71238270-71238320	HCPEpiC	choroid plexus:	n/a
41	chr11:71260323-71260373	A549	lung:	n/a
42	chr11:71238270-71238320	AG09319	gingival:	n/a
43	chr11:71259292-71259342	NT2-D1	testis:	n/a
44	chr11:71250073-71250123	SK-N-SH_RA	brain:	n/a
45	chr11:71260323-71260373	AoSMC	blood vessel:	n/a
46	chr11:71259292-71259342	GM19239	blood:	n/a
47	chr11:71248741-71248791	NH-A	brain:	n/a
48	chr11:71237522-71237572	HNPCEpiC	eye:	n/a
49	chr11:71259439-71259489	NB4	blood:	n/a
50	chr11:71248906-71248956	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr11:71253515..71257343-chr11:71260479..71262893,3	MCF-7	breast:
2	chr11:71198148..71200436-chr11:71273726..71275977,2	MCF-7	breast:
3	chr11:71189071..71191550-chr11:71272066..71273804,2	MCF-7	breast:
4	chr11:71156732..71161621-chr11:71272936..71276184,4	MCF-7	breast:
5	chr11:71253515..71257343-chr11:71260479..71262893,3	MCF-7	breast:
6	chr11:71254168..71255682-chr11:71257713..71259935,2	MCF-7	breast:
7	chr11:71209230..71212129-chr11:71251545..71253303,2	MCF-7	breast:
8	chr11:71272055..71274887-chr11:71280546..71282110,2	K562	blood:
9	chr11:71257442..71259140-chr11:71259571..71262525,2	K562	blood:
10	chr11:71159116..71165503-chr11:71274687..71279227,9	MCF-7	breast:
11	chr11:71257442..71259140-chr11:71259571..71262525,2	K562	blood:
12	chr11:71176264..71179140-chr11:71273245..71275842,2	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
ENSG00000172890	chromatin interactions
ENSG00000254997	chromatin interactions
ENSG00000254682	chromatin interactions
ENSG00000172893	chromatin interactions

Extended variants
information (count: 1731 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1731 , 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	rs74829560	chr11:71237306-71237307	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs75354897	chr11:71237318-71237319	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs78033754	chr11:71237348-71237349	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs76930048	chr11:71237365-71237366	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs371434631	chr11:71237378-71237379	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536198728	chr11:71237383-71237384	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs554848994	chr11:71237384-71237385	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566623084	chr11:71237436-71237437	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs75925844	chr11:71237439-71237440	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs78337038	chr11:71237445-71237446	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs80211050	chr11:71237448-71237449	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs77298144	chr11:71237449-71237450	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562088089	chr11:71237466-71237467	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs76604776	chr11:71237478-71237479	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs534001085	chr11:71237487-71237488	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs74995203	chr11:71237492-71237493	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs181096970	chr11:71237497-71237498	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs578170269	chr11:71237500-71237501	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs545509474	chr11:71237521-71237522	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs185733489	chr11:71237522-71237523	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs575599500	chr11:71237563-71237564	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs190507650	chr11:71237571-71237572	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs574250162	chr11:71237583-71237584	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs7114252	chr11:71237606-71237607	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs7103591	chr11:71237619-71237620	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs541129106	chr11:71237646-71237647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540452640	chr11:71237651-71237652	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs145800930	chr11:71237652-71237653	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs530643016	chr11:71237686-71237687	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs550645869	chr11:71237692-71237693	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs7130829	chr11:71237702-71237703	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs200327283	chr11:71237710-71237711	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs547849416	chr11:71237719-71237720	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs566803671	chr11:71237743-71237744	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200593146	chr11:71237749-71237750	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs534067380	chr11:71237774-71237775	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs371686085	chr11:71237812-71237813	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs10645872	chr11:71237818-71237819	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs35710928	chr11:71237819-71237820	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs10658273	chr11:71237820-71237821	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs201619143	chr11:71237821-71237822	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs558828529	chr11:71237865-71237866	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs570658015	chr11:71237955-71237956	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs537993881	chr11:71237995-71237996	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557438168	chr11:71238022-71238023	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs575614694	chr11:71238047-71238048	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs536671371	chr11:71238048-71238049	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs554644882	chr11:71238083-71238084	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs573235099	chr11:71238085-71238086	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs76060954	chr11:71238132-71238133	Enhancers Weak transcription Flanking Active TSS	TF binding 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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71232800-71243600	Weak transcription	Brain Angular Gyrus	brain
2	chr11:71232800-71245800	Weak transcription	Pancreas	Pancrea
3	chr11:71232800-71259800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:71235800-71238000	Enhancers	HepG2	liver
5	chr11:71236200-71239200	Enhancers	Liver	Liver
6	chr11:71236400-71237800	Enhancers	A549	lung
7	chr11:71236600-71237400	Enhancers	Stomach Mucosa	stomach
8	chr11:71237200-71238800	Enhancers	Fetal Intestine Large	intestine
9	chr11:71237400-71238200	Enhancers	Fetal Intestine Small	intestine
10	chr11:71238000-71238200	Flanking Active TSS	HepG2	liver
11	chr11:71238200-71238600	Active TSS	HepG2	liver
12	chr11:71238600-71239000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr11:71238600-71239000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:71238600-71239000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr11:71238600-71239200	Flanking Active TSS	HepG2	liver
16	chr11:71239000-71241400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr11:71239000-71246400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr11:71239200-71239800	Enhancers	HepG2	liver
19	chr11:71239800-71241600	Weak transcription	HepG2	liver
20	chr11:71241400-71242600	Enhancers	GM12878-XiMat	blood
21	chr11:71241400-71244400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr11:71241600-71242600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:71241600-71243400	Enhancers	HepG2	liver
24	chr11:71241800-71243600	Enhancers	K562	blood
25	chr11:71243400-71244000	Weak transcription	HepG2	liver
26	chr11:71243600-71244000	Weak transcription	K562	blood
27	chr11:71244000-71245800	Enhancers	HepG2	liver
28	chr11:71244000-71247200	Enhancers	K562	blood
29	chr11:71244400-71245200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr11:71245200-71247200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr11:71245400-71246800	Enhancers	Fetal Intestine Large	intestine
32	chr11:71245400-71247200	Enhancers	Fetal Intestine Small	intestine
33	chr11:71245400-71247400	Enhancers	Liver	Liver
34	chr11:71245800-71246400	Flanking Active TSS	HepG2	liver
35	chr11:71245800-71246600	Enhancers	Pancreas	Pancrea
36	chr11:71245800-71246800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:71246000-71246200	Enhancers	GM12878-XiMat	blood
38	chr11:71246200-71246600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr11:71246200-71247000	Weak transcription	GM12878-XiMat	blood
40	chr11:71246400-71246800	Active TSS	HepG2	liver
41	chr11:71246800-71247000	Flanking Active TSS	HepG2	liver
42	chr11:71246800-71247800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:71247000-71247400	ZNF genes & repeats	GM12878-XiMat	blood
44	chr11:71247000-71251200	Enhancers	HepG2	liver
45	chr11:71247400-71248600	Weak transcription	GM12878-XiMat	blood
46	chr11:71248600-71250600	Enhancers	GM12878-XiMat	blood
47	chr11:71249800-71250000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr11:71249800-71250000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr11:71250000-71254000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr11:71250600-71250800	Flanking Active TSS	GM12878-XiMat	blood

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