Variant report

Variant	nsv2881
Chromosome Location	chr2:113800805-113846597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:802)
CpG islands
(count:1526)
Chromatin interactive
region (count:52)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:113846123-113846581	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:113841883-113842184	K562	blood:	n/a	n/a
3	ARID3A	chr2:113837679-113838000	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:113841833-113842200	HepG2	liver:	n/a	n/a
5	ATF1	chr2:113842468-113842646	K562	blood:	n/a	n/a
6	BACH1	chr2:113830298-113830596	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr2:113808248-113808885	K562	blood:	n/a	n/a
8	BCLAF1	chr2:113808322-113808787	K562	blood:	n/a	n/a
9	BHLHE40	chr2:113841852-113842105	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:113840778-113841046	K562	blood:	n/a	n/a
11	BHLHE40	chr2:113837657-113838066	K562	blood:	n/a	n/a
12	BHLHE40	chr2:113841820-113842100	K562	blood:	n/a	n/a
13	BRCA1	chr2:113837843-113837851	HepG2	liver:	n/a	n/a
14	CBX3	chr2:113808363-113808794	K562	blood:	n/a	n/a
15	CBX3	chr2:113812744-113813121	K562	blood:	n/a	n/a
16	CBX3	chr2:113812793-113813116	K562	blood:	n/a	n/a
17	CBX3	chr2:113841780-113842272	HCT-116	colon:	n/a	n/a
18	CBX3	chr2:113808267-113808819	K562	blood:	n/a	n/a
19	CBX3	chr2:113816930-113817185	K562	blood:	n/a	chr2:113816968-113816979
20	CCNT2	chr2:113817119-113817278	K562	blood:	n/a	n/a
21	CCNT2	chr2:113808487-113808687	K562	blood:	n/a	n/a
22	CEBPB	chr2:113846307-113846455	HepG2	liver:	n/a	chr2:113846389-113846401
23	CEBPB	chr2:113813626-113813695	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:113817993-113818199	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:113835807-113836288	MCF-7	breast:	n/a	n/a
26	CEBPB	chr2:113846229-113846478	HepG2	liver:	n/a	chr2:113846389-113846401
27	CEBPB	chr2:113837776-113838100	K562	blood:	n/a	n/a
28	CEBPB	chr2:113825406-113825531	HepG2	liver:	n/a	chr2:113825428-113825439
29	CEBPB	chr2:113835560-113836255	MCF-7	breast:	n/a	n/a
30	CEBPB	chr2:113813636-113813677	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:113846209-113846551	HepG2	liver:	n/a	chr2:113846389-113846401
32	CHD2	chr2:113808657-113808709	K562	blood:	n/a	n/a
33	CTCF	chr2:113843180-113843330	HMEC	breast:	n/a	n/a
34	CTCF	chr2:113837690-113837971	GM19239	blood:	n/a	n/a
35	CTCF	chr2:113842220-113842370	HCM	heart:	n/a	n/a
36	CTCF	chr2:113837740-113837890	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr2:113841480-113841630	HEK293	kidney:	n/a	n/a
38	CTCF	chr2:113808660-113808810	HMEC	breast:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
39	CTCF	chr2:113841740-113842240	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:113808680-113808830	HCM	heart:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808682-113808695
41	CTCF	chr2:113837740-113837890	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr2:113841340-113841490	AG10803	skin:	n/a	n/a
43	CTCF	chr2:113842580-113842730	GM12865	blood:	n/a	n/a
44	CTCF	chr2:113808654-113808738	MCF-7	breast:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
45	CTCF	chr2:113842025-113842089	GM13976	blood:	n/a	n/a
46	CTCF	chr2:113837760-113837910	BJ	skin:	n/a	n/a
47	CTCF	chr2:113841859-113842224	GM12878	blood:	n/a	n/a
48	CTCF	chr2:113837760-113837910	HEK293	kidney:	n/a	n/a
49	CTCF	chr2:113829960-113830110	AoAF	blood vessel:	n/a	chr2:113830061-113830070
50	CTCF	chr2:113837780-113837930	HVMF	connective:	n/a	n/a

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113810244-113810294	MCF10A-Er-Src	breast:	n/a
2	chr2:113810244-113810294	MCF10A-Er-Src	breast:	n/a
3	chr2:113811250-113811300	NHDF-neo	bronchial:	n/a
4	chr2:113825513-113825563	PANC-1	pancreas:	n/a
5	chr2:113831203-113831253	T-47D	breast:	n/a
6	chr2:113808452-113808502	MCF10A-Er-Src	breast:	n/a
7	chr2:113825234-113825284	Caco-2	colon:	n/a
8	chr2:113830191-113830241	NB4	blood:	n/a
9	chr2:113820090-113820140	IMR90	lung:	fetal
10	chr2:113817043-113817093	GM12892	blood:	n/a
11	chr2:113817043-113817093	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:113831203-113831253	U87	brain:	n/a
13	chr2:113832957-113833007	NH-A	brain:	n/a
14	chr2:113808683-113808733	SK-N-MC	brain:	n/a
15	chr2:113820090-113820140	U87	brain:	n/a
16	chr2:113811250-113811300	HMEC	breast:	n/a
17	chr2:113837401-113837451	HCPEpiC	choroid plexus:	n/a
18	chr2:113817043-113817093	HCF	heart:	n/a
19	chr2:113811250-113811300	HL-60	blood:	n/a
20	chr2:113811250-113811300	BJ	skin:	n/a
21	chr2:113817043-113817093	HL-60	blood:	n/a
22	chr2:113810743-113810793	NT2-D1	testis:	n/a
23	chr2:113816662-113816712	NB4	blood:	n/a
24	chr2:113825302-113825352	HEK293	kidney:	embryo
25	chr2:113825513-113825563	NT2-D1	testis:	n/a
26	chr2:113808755-113808805	U87	brain:	n/a
27	chr2:113825882-113825932	BE2_C	brain:	n/a
28	chr2:113817043-113817093	HNPCEpiC	eye:	n/a
29	chr2:113817043-113817093	Hepatocyte	liver:	n/a
30	chr2:113824657-113824707	Hela-S3	cervix:	n/a
31	chr2:113829866-113829916	LNCaP	prostate:	n/a
32	chr2:113816832-113816882	PANC-1	pancreas:	n/a
33	chr2:113816662-113816712	GM12878	blood:	n/a
34	chr2:113811250-113811300	HRCEpiC	kidney:	n/a
35	chr2:113808683-113808733	Jurkat	blood:	n/a
36	chr2:113832957-113833007	Caco-2	colon:	n/a
37	chr2:113832957-113833007	HNPCEpiC	eye:	n/a
38	chr2:113820090-113820140	HCT-116	colon:	n/a
39	chr2:113808530-113808580	GM06990	blood:	n/a
40	chr2:113829468-113829518	Hepatocyte	liver:	n/a
41	chr2:113832957-113833007	MCF10A-Er-Src	breast:	n/a
42	chr2:113810743-113810793	AG04450	lung:	fetal
43	chr2:113808452-113808502	BJ	skin:	n/a
44	chr2:113816662-113816712	AG04450	lung:	fetal
45	chr2:113837401-113837451	AG04449	skin:	fetal
46	chr2:113808755-113808805	A549	lung:	n/a
47	chr2:113820090-113820140	AoSMC	blood vessel:	n/a
48	chr2:113824657-113824707	ECC-1	luminal epithelium:	n/a
49	chr2:113831203-113831253	SK-N-MC	brain:	n/a
50	chr2:113825882-113825932	HL-60	blood:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:113837325..113838487-chr2:113894163..113895181,5	K562	blood:
2	chr2:113817115..113819025-chr2:113830617..113832382,2	MCF-7	breast:
3	chr2:113835663..113838530-chr2:113914513..113916116,2	MCF-7	breast:
4	chr2:113826651..113828655-chr2:113831530..113833461,2	K562	blood:
5	chr2:113815048..113817991-chr2:113819572..113821911,4	K562	blood:
6	chr2:113798210..113800371-chr2:113830392..113832016,2	MCF-7	breast:
7	chr2:113816094..113817595-chr2:113914612..113916340,2	MCF-7	breast:
8	chr2:113840278..113841811-chr2:113847020..113849083,2	K562	blood:
9	chr2:113840604..113842115-chr2:113843174..113845209,2	K562	blood:
10	chr2:113842260..113843239-chr2:113894352..113895397,3	MCF-7	breast:
11	chr2:113842067..113843806-chr2:113845279..113847597,2	K562	blood:
12	chr2:113835964..113840226-chr2:113955452..113959687,5	MCF-7	breast:
13	chr2:113815048..113817991-chr2:113819572..113821911,4	K562	blood:
14	chr2:113840365..113842107-chr2:113890479..113892989,2	MCF-7	breast:
15	chr2:113808473..113809153-chr2:113816777..113817326,2	K562	blood:
16	chr2:113718593..113720289-chr2:113834611..113837557,2	MCF-7	breast:
17	chr2:113816411..113818730-chr2:113824215..113826075,2	K562	blood:
18	chr2:113837374..113837912-chr2:114127892..114128718,2	K562	blood:
19	chr2:113809110..113811211-chr2:113812737..113815572,2	K562	blood:
20	chr2:113836433..113838367-chr2:113961484..113963853,2	MCF-7	breast:
21	chr2:113808741..113811211-chr2:113813910..113818157,4	K562	blood:
22	chr2:113825741..113828601-chr2:113834628..113836423,2	MCF-7	breast:
23	chr2:113838578..113840540-chr2:113849414..113851474,2	MCF-7	breast:
24	chr2:113837374..113838246-chr2:113894254..113895056,3	MCF-7	breast:
25	chr2:113836933..113837467-chr2:113934054..113934934,2	MCF-7	breast:
26	chr2:113834467..113836706-chr2:113841489..113843964,2	MCF-7	breast:
27	chr2:113840473..113842575-chr2:113882514..113884830,2	MCF-7	breast:
28	chr2:113815604..113817991-chr2:113819036..113821911,2	K562	blood:
29	chr2:113827867..113831764-chr2:113833015..113836168,5	MCF-7	breast:
30	chr2:113842067..113843806-chr2:113845279..113847597,2	K562	blood:
31	chr2:113837298..113838414-chr2:113957612..113958528,4	MCF-7	breast:
32	chr2:113808741..113811211-chr2:113813910..113818157,4	K562	blood:
33	chr2:113839317..113841682-chr2:113938699..113940328,2	K562	blood:
34	chr2:113836939..113839548-chr2:113991525..113994507,2	MCF-7	breast:
35	chr2:113841554..113842111-chr2:113896078..113896943,2	MCF-7	breast:
36	chr2:113835706..113838400-chr2:113880453..113883939,3	MCF-7	breast:
37	chr2:113815604..113817991-chr2:113819036..113821911,2	K562	blood:
38	chr2:113741483..113743922-chr2:113839528..113841138,2	K562	blood:
39	chr2:113799300..113800125-chr2:113836934..113837726,3	MCF-7	breast:
40	chr2:113819021..113821885-chr2:113822119..113824184,2	MCF-7	breast:
41	chr2:113834467..113836706-chr2:113841489..113843964,2	MCF-7	breast:
42	chr2:113826166..113827834-chr2:113829745..113831406,2	K562	blood:
43	chr2:113825741..113828601-chr2:113834628..113836423,2	MCF-7	breast:
44	chr2:113819855..113821776-chr2:113826453..113828275,2	MCF-7	breast:
45	chr2:113837662..113838271-chr2:113961226..113962104,2	MCF-7	breast:
46	chr2:113837862..113838404-chr2:113956604..113957377,3	MCF-7	breast:
47	chr2:113816411..113818730-chr2:113824215..113826075,2	K562	blood:
48	chr2:113837765..113839725-chr2:113955649..113957205,2	MCF-7	breast:
49	chr2:113820207..113823045-chr2:113825463..113827849,2	MCF-7	breast:
50	chr2:113837351..113838104-chr2:114147540..114148341,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL36RN-2	chr2:113802726-113802812	l_1927_chr2:113799151-113802812_thyroid

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	IL36RN	hsa-miR-16-5p	chr2:113821266-113821272

Variant related genes	Relation type
IL36B	TF binding region
RNU6-1180P	TF binding region
IL1F10	TF binding region
IL36RN	TF binding region
IL36B	CpG island
RNU6-1180P	CpG island
IL1F10	CpG island
IL36RN	CpG island
ENSG00000125637	chromatin interactions
ENSG00000136695	chromatin interactions
ENSG00000125618	chromatin interactions
ENSG00000136697	chromatin interactions
ENSG00000201805	chromatin interactions
ENSG00000189223	chromatin interactions
ENSG00000136696	chromatin interactions

Extended variants
information (count: 1883 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1883 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563996132	chr2:113802738-113802739	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs577427483	chr2:113802747-113802748	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs77976833	chr2:113802758-113802759	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs575296721	chr2:113802764-113802765	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs146504191	chr2:113802774-113802775	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs575010389	chr2:113804610-113804611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192089826	chr2:113804660-113804661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371088220	chr2:113804674-113804675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138570520	chr2:113804694-113804695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34498045	chr2:113804744-113804745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532541175	chr2:113804745-113804746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552261559	chr2:113804780-113804781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35805200	chr2:113804791-113804792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141152799	chr2:113804806-113804807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569255726	chr2:113804821-113804822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374677144	chr2:113804836-113804837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182315566	chr2:113804837-113804838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567582865	chr2:113804847-113804848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536169546	chr2:113804879-113804880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550019365	chr2:113804912-113804913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368542435	chr2:113804921-113804922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569866817	chr2:113804930-113804931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540219713	chr2:113804993-113804994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35151387	chr2:113804996-113804997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13398479	chr2:113804997-113804998	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs371356046	chr2:113805000-113805001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558728492	chr2:113805017-113805018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539601918	chr2:113805044-113805045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189976128	chr2:113805053-113805054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537918596	chr2:113805054-113805055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555033563	chr2:113805057-113805058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575017995	chr2:113805060-113805061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534641619	chr2:113805071-113805072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10179714	chr2:113805118-113805119	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs182603414	chr2:113805136-113805137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543782334	chr2:113805163-113805164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs367668683	chr2:113805177-113805178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34645153	chr2:113805229-113805230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs113009521	chr2:113805237-113805238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545983924	chr2:113805243-113805244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150707817	chr2:113805281-113805282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542843202	chr2:113805312-113805313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34294724	chr2:113805369-113805370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542271738	chr2:113805385-113805386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553246913	chr2:113805388-113805389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561959184	chr2:113805408-113805409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573132447	chr2:113805419-113805420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183506850	chr2:113805423-113805424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549817697	chr2:113805467-113805468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188389852	chr2:113805495-113805496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113804600-113805400	Enhancers	Fetal Intestine Large	intestine
2	chr2:113804600-113805400	Enhancers	Fetal Intestine Small	intestine
3	chr2:113805400-113805600	Weak transcription	Fetal Intestine Small	intestine
4	chr2:113805400-113805800	Weak transcription	Fetal Intestine Large	intestine
5	chr2:113805600-113806000	Enhancers	Fetal Intestine Small	intestine
6	chr2:113805800-113806000	Enhancers	Fetal Intestine Large	intestine
7	chr2:113806000-113808600	Weak transcription	Fetal Intestine Large	intestine
8	chr2:113806000-113809000	Weak transcription	Fetal Intestine Small	intestine
9	chr2:113808400-113808800	Weak transcription	Right Atrium	heart
10	chr2:113808600-113811600	Enhancers	Fetal Intestine Large	intestine
11	chr2:113809000-113809200	Enhancers	Fetal Intestine Small	intestine
12	chr2:113809000-113809200	ZNF genes & repeats	Right Atrium	heart
13	chr2:113809200-113809600	Weak transcription	Fetal Intestine Small	intestine
14	chr2:113809400-113813800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:113809600-113811200	Enhancers	Fetal Intestine Small	intestine
16	chr2:113811200-113814400	ZNF genes & repeats	Fetal Intestine Small	intestine
17	chr2:113812400-113812600	Bivalent/Poised TSS	Sigmoid Colon	Sigmoid Colon
18	chr2:113812400-113812800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:113812600-113812800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr2:113813800-113814200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr2:113813800-113815200	Enhancers	Fetal Intestine Large	intestine
22	chr2:113814200-113816200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:113814400-113815000	Weak transcription	Fetal Intestine Small	intestine
24	chr2:113814600-113818400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:113815000-113815200	Enhancers	Fetal Intestine Small	intestine
26	chr2:113815000-113815200	Enhancers	Placenta	Placenta
27	chr2:113815200-113816200	Weak transcription	Placenta	Placenta
28	chr2:113815800-113817400	Enhancers	NHEK	skin
29	chr2:113816000-113817000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr2:113816000-113817000	Enhancers	HMEC	breast
31	chr2:113816000-113818400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:113816200-113816800	Enhancers	Esophagus	oesophagus
33	chr2:113816200-113817000	Enhancers	Placenta	Placenta
34	chr2:113816200-113817600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr2:113816400-113817200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr2:113816400-113817400	Enhancers	Fetal Lung	lung
37	chr2:113816400-113817800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr2:113816800-113817400	Flanking Active TSS	Esophagus	oesophagus
39	chr2:113817000-113817400	Flanking Active TSS	Placenta	Placenta
40	chr2:113817000-113818000	Weak transcription	HMEC	breast
41	chr2:113817000-113825400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:113817200-113819200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr2:113817400-113817600	Active TSS	Esophagus	oesophagus
44	chr2:113817400-113817800	Weak transcription	NHEK	skin
45	chr2:113817400-113821600	Enhancers	Placenta	Placenta
46	chr2:113817600-113826200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:113817800-113818400	Enhancers	NHEK	skin
48	chr2:113817800-113820400	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr2:113818000-113818200	Weak transcription	Esophagus	oesophagus
50	chr2:113818000-113818400	Enhancers	HMEC	breast

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