Variant report

Variant	nsv870101
Chromosome Location	chr11:19037931-19093952
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:306)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:19093741-19093747	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:19092648-19093101	K562	blood:	n/a	n/a
3	ARID3A	chr11:19092647-19093076	HepG2	liver:	n/a	n/a
4	ATF1	chr11:19092747-19093100	K562	blood:	n/a	n/a
5	ATF2	chr11:19092649-19093135	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:19092631-19093067	GM12878	blood:	n/a	n/a
7	ATF2	chr11:19092639-19093114	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr11:19092685-19093129	GM12878	blood:	n/a	chr11:19092868-19092879 chr11:19092870-19092878 chr11:19092868-19092879 chr11:19092868-19092881
9	ATF3	chr11:19092741-19093094	K562	blood:	n/a	chr11:19092868-19092879 chr11:19092870-19092878 chr11:19092868-19092879 chr11:19092868-19092881
10	BACH1	chr11:19092773-19093119	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr11:19048430-19048840	GM12878	blood:	n/a	n/a
12	BCL3	chr11:19048430-19048742	GM12878	blood:	n/a	n/a
13	BCLAF1	chr11:19092683-19093118	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:19093563-19093861	HepG2	liver:	n/a	n/a
15	BHLHE40	chr11:19093331-19093466	K562	blood:	n/a	n/a
16	BHLHE40	chr11:19092747-19093102	GM12878	blood:	n/a	n/a
17	BRCA1	chr11:19092764-19092957	HepG2	liver:	n/a	n/a
18	BRCA1	chr11:19092708-19093152	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr11:19092602-19093253	HCT-116	colon:	n/a	n/a
20	CBX3	chr11:19092718-19092997	K562	blood:	n/a	n/a
21	CBX3	chr11:19049746-19050118	HCT-116	colon:	n/a	n/a
22	CBX3	chr11:19092724-19093146	K562	blood:	n/a	n/a
23	CEBPB	chr11:19092730-19093077	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:19070911-19071248	H1-hESC	embryonic stem cell:	n/a	chr11:19071079-19071090
25	CEBPB	chr11:19075503-19075812	HepG2	liver:	n/a	chr11:19075655-19075666
26	CEBPB	chr11:19075566-19075841	MCF-7	breast:	n/a	chr11:19075655-19075666
27	CEBPB	chr11:19075550-19075793	A549	lung:	n/a	chr11:19075655-19075666
28	CEBPB	chr11:19070915-19071272	IMR90	lung:	n/a	chr11:19071079-19071090
29	CEBPB	chr11:19092703-19093066	A549	lung:	n/a	n/a
30	CEBPB	chr11:19075539-19075817	IMR90	lung:	n/a	chr11:19075655-19075666
31	CEBPB	chr11:19093404-19093603	K562	blood:	n/a	n/a
32	CEBPB	chr11:19070928-19071245	K562	blood:	n/a	chr11:19071079-19071090
33	CEBPB	chr11:19092708-19093097	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr11:19049458-19049658	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:19070121-19070197	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr11:19092733-19093067	K562	blood:	n/a	n/a
37	CEBPB	chr11:19070928-19071353	HepG2	liver:	n/a	chr11:19071079-19071090
38	CEBPB	chr11:19070945-19071259	Hela-S3	cervix:	n/a	chr11:19071079-19071090
39	CEBPB	chr11:19092732-19093066	IMR90	lung:	n/a	n/a
40	CEBPB	chr11:19075511-19075778	K562	blood:	n/a	chr11:19075655-19075666
41	CEBPB	chr11:19092787-19093018	K562	blood:	n/a	n/a
42	CEBPB	chr11:19092706-19093095	K562	blood:	n/a	n/a
43	CEBPB	chr11:19070943-19071260	A549	lung:	n/a	chr11:19071079-19071090
44	CEBPB	chr11:19092715-19093066	HepG2	liver:	n/a	n/a
45	CHD2	chr11:19092793-19093023	HepG2	liver:	n/a	n/a
46	CREB1	chr11:19092830-19093131	A549	lung:	n/a	n/a
47	CREB1	chr11:19092790-19093096	A549	lung:	n/a	n/a
48	CTCF	chr11:19092860-19093010	NHEK	skin:	n/a	chr11:19092929-19092947 chr11:19092932-19092945 chr11:19092876-19092883 chr11:19092874-19092895 chr11:19092932-19092941
49	CTCF	chr11:19092770-19093068	MCF-7	breast:	n/a	chr11:19092929-19092947 chr11:19092932-19092945 chr11:19092876-19092883 chr11:19092874-19092895 chr11:19092932-19092941
50	CTCF	chr11:19093211-19093317	GM12891	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:19081590-19081640	GM12891	blood:	n/a
2	chr11:19081590-19081640	GM12891	blood:	n/a
3	chr11:19083542-19083592	BE2_C	brain:	n/a
4	chr11:19077763-19077813	HUVEC	blood vessel:	n/a
5	chr11:19081590-19081640	A549	lung:	n/a
6	chr11:19082514-19082564	HIPEpiC	eye:	n/a
7	chr11:19083542-19083592	HEEpiC	esophagus:	n/a
8	chr11:19083542-19083592	HCT-116	colon:	n/a
9	chr11:19083542-19083592	MCF10A-Er-Src	breast:	n/a
10	chr11:19077763-19077813	Hepatocyte	liver:	n/a
11	chr11:19078052-19078102	Jurkat	blood:	n/a
12	chr11:19082514-19082564	NT2-D1	testis:	n/a
13	chr11:19083542-19083592	AoSMC	blood vessel:	n/a
14	chr11:19078052-19078102	HRE	kidney:	n/a
15	chr11:19082514-19082564	HAEpiC	amniotic membrane:	n/a
16	chr11:19082514-19082564	HRCEpiC	kidney:	n/a
17	chr11:19077763-19077813	PANC-1	pancreas:	n/a
18	chr11:19078052-19078102	T-47D	breast:	n/a
19	chr11:19083542-19083592	GM06990	blood:	n/a
20	chr11:19081590-19081640	HL-60	blood:	n/a
21	chr11:19083542-19083592	RPTEC	kidney:	n/a
22	chr11:19082514-19082564	AG04450	lung:	fetal
23	chr11:19081590-19081640	IMR90	lung:	fetal
24	chr11:19077763-19077813	ovcar-3	ovarian:	n/a
25	chr11:19078052-19078102	HMEC	breast:	n/a
26	chr11:19082514-19082564	SK-N-SH	brain:	n/a
27	chr11:19078052-19078102	SK-N-SH	brain:	n/a
28	chr11:19077763-19077813	HAEpiC	amniotic membrane:	n/a
29	chr11:19077763-19077813	Jurkat	blood:	n/a
30	chr11:19082514-19082564	Hela-S3	cervix:	n/a
31	chr11:19083542-19083592	Hela-S3	cervix:	n/a
32	chr11:19082514-19082564	HNPCEpiC	eye:	n/a
33	chr11:19081590-19081640	NH-A	brain:	n/a
34	chr11:19081590-19081640	NB4	blood:	n/a
35	chr11:19081590-19081640	Hela-S3	cervix:	n/a
36	chr11:19082514-19082564	ProgFib	skin:	n/a
37	chr11:19081590-19081640	HCPEpiC	choroid plexus:	n/a
38	chr11:19078052-19078102	HEEpiC	esophagus:	n/a
39	chr11:19078052-19078102	HCPEpiC	choroid plexus:	n/a
40	chr11:19081590-19081640	U87	brain:	n/a
41	chr11:19082514-19082564	HRPEpiC	eye:	n/a
42	chr11:19077763-19077813	GM19239	blood:	n/a
43	chr11:19078052-19078102	ProgFib	skin:	n/a
44	chr11:19081590-19081640	T-47D	breast:	n/a
45	chr11:19082514-19082564	MCF10A-Er-Src	breast:	n/a
46	chr11:19082514-19082564	AG10803	skin:	n/a
47	chr11:19083542-19083592	Hepatocyte	liver:	n/a
48	chr11:19081590-19081640	GM19239	blood:	n/a
49	chr11:19081590-19081640	ProgFib	skin:	n/a
50	chr11:19078052-19078102	HCF	heart:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:19040852..19043849-chr11:19051453..19053254,2	K562	blood:
2	chr11:19092510..19093247-chr11:19579344..19580002,2	MCF-7	breast:
3	chr11:19092474..19093535-chr11:19131007..19132483,9	MCF-7	breast:
4	chr11:19093295..19097207-chr11:19260781..19264758,3	K562	blood:
5	chr11:19092701..19093408-chr11:19575271..19576064,4	MCF-7	breast:
6	chr11:19092605..19093423-chr11:19578784..19579949,4	MCF-7	breast:
7	chr11:19092805..19093359-chr11:19763994..19764827,2	MCF-7	breast:
8	chr10:35195660..35196160-chr11:19092631..19093233,2	MCF-7	breast:
9	chr11:19092409..19092994-chr11:19579154..19579874,2	K562	blood:
10	chr11:19092645..19093311-chr5:141695576..141696096,4	MCF-7	breast:
11	chr11:19092467..19093363-chr11:19280997..19281539,2	MCF-7	breast:
12	chr11:19092526..19093289-chr11:19182527..19183071,2	MCF-7	breast:
13	chr11:19092484..19094846-chr11:19096156..19098835,2	MCF-7	breast:
14	chr11:19092311..19093429-chr11:19574985..19576236,16	MCF-7	breast:
15	chr11:19092338..19093322-chr11:19281072..19281919,3	K562	blood:
16	chr11:19093222..19095138-chr11:19125990..19128293,2	MCF-7	breast:
17	chr11:19092482..19093281-chr11:19347628..19348265,2	MCF-7	breast:
18	chr11:19091906..19093550-chr11:19574860..19576001,19	K562	blood:
19	chr11:19092362..19093374-chr11:19131560..19132799,3	MCF-7	breast:
20	chr11:19081397..19083267-chr11:19138143..19140482,2	MCF-7	breast:
21	chr11:19092360..19092956-chr11:19138799..19139467,2	MCF-7	breast:
22	chr11:18948757..18949726-chr11:19092570..19093333,3	MCF-7	breast:
23	chr10:35195660..35196180-chr11:19092642..19093348,2	MCF-7	breast:
24	chr11:19092441..19093031-chr11:19138770..19139494,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRGPRX2-1	chr11:19051244-19051985	NONHSAT018325

No data

Variant related genes	Relation type
ENSG00000255424	TF binding region
MRGPRX2	TF binding region
ENSG00000255424	CpG island
MRGPRX2	CpG island
ENSG00000177054	chromatin interactions
ENSG00000129173	chromatin interactions
ENSG00000255424	chromatin interactions

Extended variants
information (count: 739 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569773317	chr11:19040853-19040854	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs115369222	chr11:19040881-19040882	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs141904590	chr11:19040882-19040883	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568376344	chr11:19040948-19040949	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs561684973	chr11:19040972-19040973	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573562179	chr11:19041032-19041033	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371768008	chr11:19041033-19041034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs540674393	chr11:19041037-19041038	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554037030	chr11:19041101-19041102	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530976350	chr11:19041119-19041120	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529175975	chr11:19041137-19041138	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs35110586	chr11:19041180-19041181	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375173320	chr11:19041183-19041184	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572367225	chr11:19041188-19041189	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10766523	chr11:19041203-19041204	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184806634	chr11:19041242-19041243	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs188095919	chr11:19041261-19041262	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150629577	chr11:19041292-19041293	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs34716026	chr11:19041327-19041328	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113121872	chr11:19041328-19041329	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs16936009	chr11:19041394-19041395	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs375855804	chr11:19041450-19041451	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12292273	chr11:19041455-19041456	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs74815561	chr11:19041512-19041513	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559788017	chr11:19041526-19041527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10833043	chr11:19041527-19041528	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs114407433	chr11:19041548-19041549	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs191345181	chr11:19041551-19041552	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs112465449	chr11:19041579-19041580	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs138727495	chr11:19041585-19041586	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565585474	chr11:19041665-19041666	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549061640	chr11:19041685-19041686	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs567291456	chr11:19041693-19041694	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534424478	chr11:19041726-19041727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184781299	chr11:19041753-19041754	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577231603	chr11:19041760-19041761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539726300	chr11:19041865-19041866	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373029121	chr11:19041894-19041895	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576574879	chr11:19041932-19041933	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543694283	chr11:19041952-19041953	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189596567	chr11:19041982-19041983	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574135857	chr11:19041983-19041984	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541559402	chr11:19041995-19041996	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369011674	chr11:19042053-19042054	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533400696	chr11:19042059-19042060	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551632292	chr11:19042061-19042062	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs563482874	chr11:19042063-19042064	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143049812	chr11:19042126-19042127	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs118049145	chr11:19042130-19042131	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs115081577	chr11:19042152-19042153	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:19045400-19048000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr11:19045600-19048400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr11:19045800-19046000	Bivalent Enhancer	HMEC	breast
4	chr11:19046000-19046200	Bivalent Enhancer	HUVEC	blood vessel
5	chr11:19046400-19048800	Enhancers	Fetal Heart	heart
6	chr11:19046600-19046800	Bivalent Enhancer	Brain Germinal Matrix	brain
7	chr11:19046600-19050600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr11:19046800-19048200	Enhancers	Brain Germinal Matrix	brain
9	chr11:19047000-19047200	Enhancers	Right Atrium	heart
10	chr11:19047000-19047400	Bivalent Enhancer	Fetal Brain Female	brain
11	chr11:19047000-19047800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:19047000-19048000	Enhancers	HUVEC	blood vessel
13	chr11:19047200-19048000	Weak transcription	Right Atrium	heart
14	chr11:19047200-19048800	Enhancers	NHDF-Ad	bronchial
15	chr11:19047200-19050000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr11:19047400-19047600	Enhancers	Fetal Brain Male	brain
17	chr11:19047400-19047600	Bivalent Enhancer	HMEC	breast
18	chr11:19047400-19047800	Enhancers	Fetal Brain Female	brain
19	chr11:19047400-19048000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr11:19047600-19047800	Flanking Active TSS	Fetal Brain Male	brain
21	chr11:19047600-19047800	Enhancers	NHEK	skin
22	chr11:19047600-19048800	Enhancers	Left Ventricle	heart
23	chr11:19047800-19048000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:19047800-19048000	Enhancers	Fetal Brain Male	brain
25	chr11:19047800-19048600	Enhancers	Stomach Mucosa	stomach
26	chr11:19048000-19048400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:19048000-19048800	Enhancers	Right Atrium	heart
28	chr11:19048000-19049400	Weak transcription	HUVEC	blood vessel
29	chr11:19048200-19048600	Bivalent Enhancer	HMEC	breast
30	chr11:19048400-19049800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:19048400-19050800	Enhancers	NHEK	skin
32	chr11:19048600-19048800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:19048600-19049600	Weak transcription	Stomach Mucosa	stomach
34	chr11:19048600-19050600	Enhancers	HMEC	breast
35	chr11:19048800-19049600	Weak transcription	NHDF-Ad	bronchial
36	chr11:19048800-19050000	Enhancers	NH-A	brain
37	chr11:19048800-19050600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:19048800-19050600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr11:19049400-19049800	Enhancers	Hela-S3	cervix
40	chr11:19049600-19049800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:19049600-19049800	Enhancers	HUVEC	blood vessel
42	chr11:19049600-19049800	Enhancers	NHDF-Ad	bronchial
43	chr11:19049600-19049800	Flanking Active TSS	Osteobl	bone
44	chr11:19049600-19050000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr11:19049600-19050000	Enhancers	Esophagus	oesophagus
46	chr11:19049600-19050000	Enhancers	Stomach Mucosa	stomach
47	chr11:19049800-19050400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr11:19050400-19051800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr11:19051200-19051800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr11:19076200-19076800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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