Variant report

Variant	nsv825266
Chromosome Location	chr10:19807019-20037182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:980)
CpG islands
(count:488)
Chromatin interactive
region (count:16)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:19927475-19927788	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:19928010-19928135	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:19945416-19945759	HepG2	liver:	n/a	n/a
4	ATF1	chr10:20031092-20031318	K562	blood:	n/a	n/a
5	ATF1	chr10:20019092-20019388	K562	blood:	n/a	n/a
6	ATF1	chr10:20024073-20024273	K562	blood:	n/a	n/a
7	BACH1	chr10:19836112-19836113	K562	blood:	n/a	n/a
8	BACH1	chr10:19867582-19867705	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr10:20035644-20035814	GM12878	blood:	n/a	n/a
10	BATF	chr10:19807634-19807887	GM12878	blood:	n/a	chr10:19807691-19807699
11	BATF	chr10:20035664-20035859	GM12878	blood:	n/a	n/a
12	BCL11A	chr10:20036910-20037233	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:20035655-20035827	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:19807647-19807851	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:20035672-20035886	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:20036959-20037247	HepG2	liver:	n/a	n/a
17	BHLHE40	chr10:20035652-20035896	HepG2	liver:	n/a	n/a
18	BRCA1	chr10:19884779-19884781	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:19867948-19868304	HepG2	liver:	n/a	chr10:19868119-19868132 chr10:19868201-19868218 chr10:19868119-19868130
20	CEBPB	chr10:19940438-19941029	IMR90	lung:	n/a	chr10:19940638-19940649
21	CEBPB	chr10:20002775-20003063	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr10:19940544-19940874	MCF-7	breast:	n/a	chr10:19940638-19940649
23	CEBPB	chr10:19927464-19927923	MCF-7	breast:	n/a	chr10:19927714-19927725
24	CEBPB	chr10:19867958-19868244	A549	lung:	n/a	chr10:19868119-19868132 chr10:19868201-19868218 chr10:19868119-19868130
25	CEBPB	chr10:19923178-19923460	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:19918561-19918761	HepG2	liver:	n/a	chr10:19918689-19918700 chr10:19918691-19918702
27	CEBPB	chr10:19936413-19936751	A549	lung:	n/a	chr10:19936565-19936576 chr10:19936564-19936575 chr10:19936566-19936575
28	CEBPB	chr10:20023681-20023947	HepG2	liver:	n/a	n/a
29	CEBPB	chr10:19929221-19929407	HepG2	liver:	n/a	chr10:19929358-19929371 chr10:19929358-19929369
30	CEBPB	chr10:19929221-19929493	IMR90	lung:	n/a	chr10:19929358-19929371 chr10:19929358-19929369
31	CEBPB	chr10:19859072-19859448	HepG2	liver:	n/a	chr10:19859255-19859268 chr10:19859256-19859267 chr10:19859255-19859266 chr10:19859255-19859268 chr10:19859308-19859319
32	CEBPB	chr10:19835213-19835386	H1-hESC	embryonic stem cell:	n/a	chr10:19835318-19835331 chr10:19835318-19835329 chr10:19835320-19835331 chr10:19835318-19835331
33	CEBPB	chr10:20023742-20023942	A549	lung:	n/a	n/a
34	CEBPB	chr10:19945429-19945775	IMR90	lung:	n/a	n/a
35	CEBPB	chr10:19923117-19923490	HepG2	liver:	n/a	n/a
36	CEBPB	chr10:19835154-19835476	HepG2	liver:	n/a	chr10:19835318-19835331 chr10:19835318-19835329 chr10:19835320-19835331 chr10:19835318-19835331
37	CEBPB	chr10:19991211-19991537	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:19936399-19936732	HepG2	liver:	n/a	chr10:19936565-19936576 chr10:19936564-19936575 chr10:19936566-19936575
39	CEBPB	chr10:19945428-19945658	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:19838464-19838764	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr10:19859086-19859357	K562	blood:	n/a	chr10:19859255-19859268 chr10:19859256-19859267 chr10:19859255-19859266 chr10:19859255-19859268 chr10:19859308-19859319
42	CEBPB	chr10:19917762-19918070	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr10:19859084-19859439	IMR90	lung:	n/a	chr10:19859255-19859268 chr10:19859256-19859267 chr10:19859255-19859266 chr10:19859255-19859268 chr10:19859308-19859319
44	CEBPB	chr10:20005435-20005535	A549	lung:	n/a	n/a
45	CEBPB	chr10:19918532-19918884	IMR90	lung:	n/a	chr10:19918689-19918700 chr10:19918691-19918702
46	CEBPB	chr10:19940473-19940806	A549	lung:	n/a	chr10:19940638-19940649
47	CEBPB	chr10:19918971-19918989	A549	lung:	n/a	n/a
48	CEBPB	chr10:20006851-20006880	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:19996466-19996579	A549	lung:	n/a	chr10:19996526-19996537 chr10:19996526-19996539
50	CEBPB	chr10:19867955-19868271	IMR90	lung:	n/a	chr10:19868119-19868132 chr10:19868201-19868218 chr10:19868119-19868130

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:19918310-19918360	HCF	heart:	n/a
2	chr10:20023014-20023064	CMK	blood:	n/a
3	chr10:20009221-20009271	T-47D	breast:	n/a
4	chr10:20023014-20023064	BE2_C	brain:	n/a
5	chr10:19993393-19993443	HEK293	kidney:	embryo
6	chr10:19918310-19918360	PrEC	prostate:	n/a
7	chr10:20023014-20023064	Hela-S3	cervix:	n/a
8	chr10:20023014-20023064	Caco-2	colon:	n/a
9	chr10:19946093-19946143	AG09309	skin:	n/a
10	chr10:20017996-20018046	SK-N-SH_RA	brain:	n/a
11	chr10:20017996-20018046	HEEpiC	esophagus:	n/a
12	chr10:20023014-20023064	PANC-1	pancreas:	n/a
13	chr10:19946093-19946143	PFSK-1	brain:	n/a
14	chr10:19946093-19946143	HEK293	kidney:	embryo
15	chr10:20019641-20019691	HCPEpiC	choroid plexus:	n/a
16	chr10:19918310-19918360	ovcar-3	ovarian:	n/a
17	chr10:19918310-19918360	NHDF-neo	bronchial:	n/a
18	chr10:20023014-20023064	AG04450	lung:	fetal
19	chr10:20009221-20009271	AG10803	skin:	n/a
20	chr10:20009221-20009271	NT2-D1	testis:	n/a
21	chr10:19972179-19972229	PrEC	prostate:	n/a
22	chr10:19972179-19972229	T-47D	breast:	n/a
23	chr10:20017996-20018046	HUVEC	blood vessel:	n/a
24	chr10:20023014-20023064	HCF	heart:	n/a
25	chr10:19918310-19918360	BJ	skin:	n/a
26	chr10:19993393-19993443	AG04449	skin:	fetal
27	chr10:19972179-19972229	HMEC	breast:	n/a
28	chr10:19972179-19972229	NHBE	bronchial:	n/a
29	chr10:20023014-20023064	U87	brain:	n/a
30	chr10:20017996-20018046	Jurkat	blood:	n/a
31	chr10:19918310-19918360	HIPEpiC	eye:	n/a
32	chr10:19918310-19918360	HCT-116	colon:	n/a
33	chr10:19946093-19946143	HNPCEpiC	eye:	n/a
34	chr10:20023014-20023064	SK-N-SH	brain:	n/a
35	chr10:19993393-19993443	SK-N-MC	brain:	n/a
36	chr10:19918310-19918360	AG04449	skin:	fetal
37	chr10:19946093-19946143	T-47D	breast:	n/a
38	chr10:20023014-20023064	PFSK-1	brain:	n/a
39	chr10:19946093-19946143	U87	brain:	n/a
40	chr10:20023014-20023064	HRE	kidney:	n/a
41	chr10:19946093-19946143	HCPEpiC	choroid plexus:	n/a
42	chr10:19972179-19972229	HNPCEpiC	eye:	n/a
43	chr10:20019641-20019691	AG04450	lung:	fetal
44	chr10:20023014-20023064	BJ	skin:	n/a
45	chr10:20009221-20009271	CMK	blood:	n/a
46	chr10:20023014-20023064	GM19239	blood:	n/a
47	chr10:20019641-20019691	LNCaP	prostate:	n/a
48	chr10:19972179-19972229	AoSMC	blood vessel:	n/a
49	chr10:20017996-20018046	PrEC	prostate:	n/a
50	chr10:19993393-19993443	AoSMC	blood vessel:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:19806044..19808111-chr10:19811941..19813567,2	K562	blood:
2	chr10:19928272..19930845-chr10:19944987..19947653,2	K562	blood:
3	chr10:19874981..19877744-chr10:19939869..19941893,2	MCF-7	breast:
4	chr10:20020129..20021732-chr10:20034774..20036880,2	MCF-7	breast:
5	chr10:19884872..19887449-chr10:19896760..19899723,2	MCF-7	breast:
6	chr1:114251553..114252290-chr10:19972729..19973619,2	MCF-7	breast:
7	chr10:19813535..19816224-chr10:19819107..19822084,2	MCF-7	breast:
8	chr10:19943628..19945748-chr10:19960912..19962861,2	K562	blood:
9	chr10:19814024..19815559-chr10:19817040..19818969,2	K562	blood:
10	chr10:19813535..19816224-chr10:19819107..19822084,2	MCF-7	breast:
11	chr10:19806044..19808111-chr10:19811941..19813567,2	K562	blood:
12	chr10:19928272..19930845-chr10:19944987..19947653,2	K562	blood:
13	chr10:19814024..19815559-chr10:19817040..19818969,2	K562	blood:
14	chr10:19874981..19877744-chr10:19939869..19941893,2	MCF-7	breast:
15	chr10:19943628..19945748-chr10:19960912..19962861,2	K562	blood:
16	chr10:20019487..20021486-chr10:20023021..20025929,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.2
2	lnc-C10orf112-1	chr10:19981387-19981483	NONHSAT011665
3	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.2
4	lnc-NEBL-2	chr10:19999257-20000217	ENSG00000233968.1
5	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1
6	lnc-C10orf112-1	chr10:19981239-19981290	NONHSAT011665
7	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.1
8	lnc-NEBL-2	chr10:20010907-20011154	ENSG00000233968.1
9	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.2
10	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.1
11	lnc-NEBL-2	chr10:20011259-20011517	ENSG00000233968.1
12	lnc-PLXDC2-4	chr10:19887176-19887391	NONHSAT011663
13	lnc-NEBL-2	chr10:20011043-20011154	ENSG00000233968.1
14	lnc-NEBL-2	chr10:20010626-20011154	ENSG00000233968.1
15	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1
16	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.1
17	lnc-NEBL-2	chr10:20010517-20011154	ENSG00000233968.2
18	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1
19	lnc-NEBL-2	chr10:20005728-20005819	ENSG00000233968.1
20	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.1

No data

Variant related genes	Relation type
MALRD1	TF binding region
RNA5SP303	TF binding region
MTND2P16	TF binding region
ENSG00000233968	TF binding region
ENSG00000200545	TF binding region
MALRD1	CpG island
RNA5SP303	CpG island
MTND2P16	CpG island
ENSG00000233968	CpG island
ENSG00000200545	CpG island
ENSG00000230818	chromatin interactions
ENSG00000200545	chromatin interactions
ENSG00000204740	chromatin interactions

Extended variants
information (count: 10219 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:10219 , 50 per page) page: 1 2 3 4 5 6 7 ... 205

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531675207	chr10:19807025-19807026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139243682	chr10:19807079-19807080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568136498	chr10:19807101-19807102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535410633	chr10:19807134-19807135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547784660	chr10:19807135-19807136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530301494	chr10:19807173-19807174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566353228	chr10:19807177-19807178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539692575	chr10:19807182-19807183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13377162	chr10:19807332-19807333	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs576091805	chr10:19807359-19807360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11010227	chr10:19807401-19807402	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs145336559	chr10:19807414-19807415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376735267	chr10:19807415-19807416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573684857	chr10:19807449-19807450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113821773	chr10:19807483-19807484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540989985	chr10:19807496-19807497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574871104	chr10:19807516-19807517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541919943	chr10:19807589-19807590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs61841396	chr10:19807591-19807592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147250223	chr10:19807593-19807594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201258931	chr10:19807594-19807595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552699202	chr10:19807615-19807616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11813490	chr10:19807620-19807621	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs11813491	chr10:19807623-19807624	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs377590139	chr10:19807665-19807666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192757788	chr10:19807680-19807681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184820260	chr10:19807705-19807706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17793004	chr10:19807722-19807723	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs189332328	chr10:19807742-19807743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180880076	chr10:19807768-19807769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144725498	chr10:19807776-19807777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566273639	chr10:19807819-19807820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7905333	chr10:19807820-19807821	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184880605	chr10:19807822-19807823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10494868	chr10:19807875-19807876	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs145812044	chr10:19807885-19807886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs17200688	chr10:19807926-19807927	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs7905457	chr10:19807946-19807947	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370674919	chr10:19807963-19807964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79866639	chr10:19807978-19807979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552916161	chr10:19807980-19807981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569251802	chr10:19808039-19808040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371130528	chr10:19808041-19808042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577529753	chr10:19808062-19808063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545309406	chr10:19808071-19808072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556929031	chr10:19808119-19808120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575105156	chr10:19808131-19808132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7905735	chr10:19808137-19808138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34145118	chr10:19808138-19808139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561893563	chr10:19808142-19808143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intracranial aneurysm	16715129	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19796200-19839400	Weak transcription	Aorta	Aorta
2	chr10:19806800-19821800	Weak transcription	Fetal Intestine Large	intestine
3	chr10:19807400-19808000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr10:19807400-19821000	Weak transcription	Fetal Intestine Small	intestine
5	chr10:19818800-19827000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr10:19819600-19820400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr10:19819800-19820400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:19819800-19822600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr10:19820000-19820400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:19821000-19821400	Strong transcription	Fetal Intestine Small	intestine
11	chr10:19821400-19822400	Weak transcription	Fetal Intestine Small	intestine
12	chr10:19821800-19825400	Strong transcription	Fetal Intestine Large	intestine
13	chr10:19822400-19822800	Strong transcription	Fetal Intestine Small	intestine
14	chr10:19822800-19823800	Weak transcription	Fetal Intestine Small	intestine
15	chr10:19822800-19825800	Weak transcription	Fetal Lung	lung
16	chr10:19823800-19824200	Strong transcription	Fetal Intestine Small	intestine
17	chr10:19824200-19839400	Weak transcription	Fetal Intestine Small	intestine
18	chr10:19825400-19832400	Weak transcription	Fetal Intestine Large	intestine
19	chr10:19832000-19832800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr10:19832200-19833000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr10:19832400-19832800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr10:19832400-19832800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr10:19832400-19832800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr10:19832400-19833000	Strong transcription	Fetal Intestine Large	intestine
25	chr10:19833000-19833400	Weak transcription	Fetal Intestine Large	intestine
26	chr10:19833400-19834000	Strong transcription	Fetal Intestine Large	intestine
27	chr10:19834000-19840000	Weak transcription	Fetal Intestine Large	intestine
28	chr10:19835000-19836600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr10:19837800-19838200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr10:19838000-19838400	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr10:19838000-19838800	Enhancers	Colon Smooth Muscle	Colon
32	chr10:19839400-19839600	ZNF genes & repeats	Aorta	Aorta
33	chr10:19839400-19839800	ZNF genes & repeats	Fetal Intestine Small	intestine
34	chr10:19839600-19840000	Weak transcription	Aorta	Aorta
35	chr10:19839800-19875400	Weak transcription	Fetal Intestine Small	intestine
36	chr10:19840000-19840400	ZNF genes & repeats	Fetal Intestine Large	intestine
37	chr10:19840400-19856400	Weak transcription	Fetal Intestine Large	intestine
38	chr10:19850000-19850200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr10:19850200-19850800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr10:19850400-19850600	Enhancers	Fetal Brain Male	brain
41	chr10:19850800-19851600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:19851600-19858800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr10:19852400-19852800	Enhancers	Brain Germinal Matrix	brain
44	chr10:19852400-19853000	Enhancers	Aorta	Aorta
45	chr10:19852600-19853000	Enhancers	Fetal Brain Male	brain
46	chr10:19853000-19866400	Weak transcription	Aorta	Aorta
47	chr10:19856400-19857200	Strong transcription	Fetal Intestine Large	intestine
48	chr10:19857200-19861800	Weak transcription	Fetal Intestine Large	intestine
49	chr10:19858800-19859000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr10:19859000-19859200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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