Variant report

Variant	nsv1037092
Chromosome Location	chr11:71443870-71527699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2326)
CpG islands
(count:1406)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2326 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
2	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
3	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
5	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
6	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
7	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
8	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
9	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
10	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
12	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
13	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
14	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
15	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
16	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
17	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
18	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
19	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
20	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
21	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
22	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
23	BCL11A	chr11:71498840-71499221	GM12878	blood:	n/a	chr11:71498863-71498876
24	BCL11A	chr11:71497628-71497822	GM12878	blood:	n/a	n/a
25	BCL11A	chr11:71511333-71511561	GM12878	blood:	n/a	n/a
26	BCL11A	chr11:71503781-71503969	GM12878	blood:	n/a	n/a
27	BCL11A	chr11:71445521-71445844	GM12878	blood:	n/a	n/a
28	BCL11A	chr11:71473978-71474126	GM12878	blood:	n/a	n/a
29	BCL11A	chr11:71511419-71511802	GM12878	blood:	n/a	n/a
30	BCL11A	chr11:71498971-71499169	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:71499963-71500296	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:71457382-71457727	GM12878	blood:	n/a	n/a
33	BHLHE40	chr11:71511560-71511619	K562	blood:	n/a	n/a
34	BHLHE40	chr11:71460130-71460465	K562	blood:	n/a	n/a
35	BHLHE40	chr11:71524868-71525086	GM12878	blood:	n/a	n/a
36	BHLHE40	chr11:71511539-71511623	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:71475943-71476039	K562	blood:	n/a	n/a
38	BHLHE40	chr11:71498674-71498871	K562	blood:	n/a	n/a
39	BHLHE40	chr11:71497560-71498099	HepG2	liver:	n/a	n/a
40	BHLHE40	chr11:71497790-71498250	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:71498981-71499167	HepG2	liver:	n/a	n/a
42	BHLHE40	chr11:71454564-71454761	K562	blood:	n/a	n/a
43	BHLHE40	chr11:71498569-71498859	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:71497885-71498210	K562	blood:	n/a	n/a
45	BRCA1	chr11:71498122-71498649	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr11:71475856-71475966	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr11:71499265-71499372	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr11:71483127-71483599	K562	blood:	n/a	n/a
49	CBX3	chr11:71511474-71511747	K562	blood:	n/a	n/a
50	CBX3	chr11:71454384-71455190	K562	blood:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71524971-71525021	U87	brain:	n/a
2	chr11:71502816-71502866	GM12891	blood:	n/a
3	chr11:71524734-71524784	HL-60	blood:	n/a
4	chr11:71524971-71525021	U87	brain:	n/a
5	chr11:71502816-71502866	GM12891	blood:	n/a
6	chr11:71524734-71524784	HL-60	blood:	n/a
7	chr11:71524540-71524590	Hela-S3	cervix:	n/a
8	chr11:71498609-71498659	HEK293	kidney:	embryo
9	chr11:71493933-71493983	AG09309	skin:	n/a
10	chr11:71511486-71511536	AG04450	lung:	fetal
11	chr11:71456947-71456997	HRCEpiC	kidney:	n/a
12	chr11:71456947-71456997	Jurkat	blood:	n/a
13	chr11:71462582-71462632	IMR90	lung:	fetal
14	chr11:71497575-71497625	A549	lung:	n/a
15	chr11:71498202-71498252	Hepatocyte	liver:	n/a
16	chr11:71502816-71502866	HCPEpiC	choroid plexus:	n/a
17	chr11:71511486-71511536	MCF-7	breast:	n/a
18	chr11:71493933-71493983	U87	brain:	n/a
19	chr11:71511486-71511536	HRCEpiC	kidney:	n/a
20	chr11:71498715-71498765	HepG2	liver:	n/a
21	chr11:71502816-71502866	AG04449	skin:	fetal
22	chr11:71499006-71499056	AG04449	skin:	fetal
23	chr11:71497688-71497738	GM12892	blood:	n/a
24	chr11:71462582-71462632	HCT-116	colon:	n/a
25	chr11:71457160-71457210	Hepatocyte	liver:	n/a
26	chr11:71462549-71462599	HepG2	liver:	n/a
27	chr11:71502816-71502866	BJ	skin:	n/a
28	chr11:71522461-71522511	SAEC	small airway:	n/a
29	chr11:71522461-71522511	SK-N-SH	brain:	n/a
30	chr11:71462149-71462199	BJ	skin:	n/a
31	chr11:71522461-71522511	HRCEpiC	kidney:	n/a
32	chr11:71502816-71502866	Hepatocyte	liver:	n/a
33	chr11:71524500-71524550	SK-N-MC	brain:	n/a
34	chr11:71497688-71497738	ProgFib	skin:	n/a
35	chr11:71499006-71499056	HRE	kidney:	n/a
36	chr11:71498609-71498659	RPTEC	kidney:	n/a
37	chr11:71524971-71525021	GM12878	blood:	n/a
38	chr11:71502816-71502866	NB4	blood:	n/a
39	chr11:71462582-71462632	HRCEpiC	kidney:	n/a
40	chr11:71462582-71462632	PFSK-1	brain:	n/a
41	chr11:71498202-71498252	AG09309	skin:	n/a
42	chr11:71497552-71497602	Hepatocyte	liver:	n/a
43	chr11:71499117-71499167	HAEpiC	amniotic membrane:	n/a
44	chr11:71498202-71498252	GM12891	blood:	n/a
45	chr11:71493933-71493983	A549	lung:	n/a
46	chr11:71462149-71462199	Hepatocyte	liver:	n/a
47	chr11:71524734-71524784	NH-A	brain:	n/a
48	chr11:71457160-71457210	ProgFib	skin:	n/a
49	chr11:71498609-71498659	NB4	blood:	n/a
50	chr11:71485830-71485880	T-47D	breast:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3
2	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713
3	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713

No data

Variant related genes	Relation type
FAM86C1	TF binding region
ENSG00000248671	TF binding region
ENSG00000264091	TF binding region
ALG1L9P	TF binding region
FAM86C1	CpG island
ENSG00000248671	CpG island
ENSG00000264091	CpG island
ALG1L9P	CpG island
ENSG00000158483	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000118894	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000244026	chromatin interactions
ENSG00000160172	chromatin interactions

Extended variants
information (count: 4255 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:4255 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573373494	chr11:71443872-71443873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs61891862	chr11:71443878-71443879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138377078	chr11:71443884-71443885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546886925	chr11:71443891-71443892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61891863	chr11:71443903-71443904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188400414	chr11:71443943-71443944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368500588	chr11:71443944-71443945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs193192190	chr11:71443952-71443953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568348087	chr11:71443975-71443976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376918129	chr11:71443983-71443984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10898489	chr11:71444016-71444017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12284378	chr11:71444043-71444044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187996972	chr11:71444046-71444047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192421355	chr11:71444078-71444079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs202048523	chr11:71444102-71444103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372548272	chr11:71444103-71444104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544239376	chr11:71444117-71444118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183848351	chr11:71444128-71444129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189291943	chr11:71444186-71444187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181286247	chr11:71444188-71444189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12279882	chr11:71444193-71444194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs144443770	chr11:71444200-71444201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373530437	chr11:71444201-71444202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546040888	chr11:71444220-71444221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185071870	chr11:71444222-71444223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10898491	chr11:71444253-71444254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376049084	chr11:71444256-71444257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10898492	chr11:71444258-71444259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71467451	chr11:71444259-71444260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs59758292	chr11:71444275-71444276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs57984285	chr11:71444282-71444283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs56658996	chr11:71444283-71444284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201206837	chr11:71444349-71444350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549831026	chr11:71444350-71444351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201958998	chr11:71444351-71444352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs57179220	chr11:71444355-71444356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201109432	chr11:71444359-71444360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200226473	chr11:71444374-71444375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115489099	chr11:71444407-71444408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189533279	chr11:71444410-71444411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78172139	chr11:71444417-71444418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs57206725	chr11:71444424-71444425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137919735	chr11:71444428-71444429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60766946	chr11:71444436-71444437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200281166	chr11:71444468-71444469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201060631	chr11:71444497-71444498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56933119	chr11:71444516-71444517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185784637	chr11:71444522-71444523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199642285	chr11:71444527-71444528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56361830	chr11:71444528-71444529	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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 ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71434800-71449000	Weak transcription	Fetal Intestine Small	intestine
2	chr11:71442600-71446000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:71445800-71446400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr11:71445800-71446600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr11:71445800-71446600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr11:71446000-71446800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr11:71446000-71447200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:71446400-71447600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr11:71447200-71447600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:71447600-71447800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:71447600-71447800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr11:71447600-71449800	Enhancers	K562	blood
13	chr11:71449000-71449600	ZNF genes & repeats	Fetal Intestine Small	intestine
14	chr11:71449600-71459400	Weak transcription	Fetal Intestine Small	intestine
15	chr11:71449800-71451000	Weak transcription	K562	blood
16	chr11:71451000-71455000	Enhancers	K562	blood
17	chr11:71451000-71464200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:71451600-71454000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:71451800-71456000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:71453400-71453800	Enhancers	Primary hematopoietic stem cells	blood
21	chr11:71454000-71454800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:71454400-71454600	Enhancers	Fetal Lung	lung
23	chr11:71454400-71456800	Enhancers	Stomach Mucosa	stomach
24	chr11:71454800-71455400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:71455000-71455600	Flanking Active TSS	K562	blood
26	chr11:71455600-71456400	Active TSS	K562	blood
27	chr11:71455800-71456200	Enhancers	Duodenum Mucosa	Duodenum
28	chr11:71456200-71456600	Enhancers	Pancreas	Pancrea
29	chr11:71456200-71456800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
30	chr11:71456400-71456600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:71456400-71456800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr11:71456400-71456800	Enhancers	NHEK	skin
33	chr11:71456400-71457000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr11:71456400-71457200	Enhancers	K562	blood
35	chr11:71456400-71457400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:71456600-71457400	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr11:71456600-71457400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr11:71456600-71457400	Active TSS	Pancreas	Pancrea
39	chr11:71457000-71457400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:71457000-71457400	Active TSS	Colonic Mucosa	Colon
41	chr11:71457000-71457400	Active TSS	Duodenum Mucosa	Duodenum
42	chr11:71457000-71457400	Active TSS	Esophagus	oesophagus
43	chr11:71457000-71457400	Active TSS	Rectal Mucosa Donor 29	rectum
44	chr11:71457000-71457400	Active TSS	Rectal Mucosa Donor 31	rectum
45	chr11:71457000-71457400	Enhancers	HMEC	breast
46	chr11:71457000-71457400	Active TSS	NHEK	skin
47	chr11:71457200-71459600	Weak transcription	K562	blood
48	chr11:71457400-71458800	Weak transcription	Duodenum Mucosa	Duodenum
49	chr11:71457400-71460200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr11:71457400-71460200	Weak transcription	NHEK	skin

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