Variant report

Variant	esv3451326
Chromosome Location	chr2:98289174-98304076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:0)
Chromatin interactive
region (count:21)
LncRNA
region (count:54)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:98290034-98290886	K562	blood:	n/a	n/a
2	ARID3A	chr2:98294924-98295124	K562	blood:	n/a	n/a
3	ATF1	chr2:98289774-98290894	K562	blood:	n/a	n/a
4	ATF2	chr2:98290274-98290771	GM12878	blood:	n/a	n/a
5	ATF2	chr2:98290233-98290789	GM12878	blood:	n/a	n/a
6	BACH1	chr2:98294882-98295200	K562	blood:	n/a	n/a
7	BACH1	chr2:98290384-98291178	K562	blood:	n/a	n/a
8	BATF	chr2:98293136-98293395	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:98290335-98290707	GM12878	blood:	n/a	n/a
10	BCL3	chr2:98290343-98290702	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:98291568-98291729	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:98291164-98291465	K562	blood:	n/a	n/a
13	BHLHE40	chr2:98289690-98290897	K562	blood:	n/a	n/a
14	BHLHE40	chr2:98290426-98290939	GM12878	blood:	n/a	n/a
15	CBX3	chr2:98289713-98290370	K562	blood:	n/a	n/a
16	CCNT2	chr2:98289981-98290644	K562	blood:	n/a	chr2:98290258-98290278
17	CEBPB	chr2:98290301-98290908	GM12878	blood:	n/a	n/a
18	CEBPB	chr2:98294205-98294270	K562	blood:	n/a	n/a
19	CEBPB	chr2:98294796-98295063	K562	blood:	n/a	n/a
20	CEBPD	chr2:98289991-98290393	K562	blood:	n/a	n/a
21	CHD2	chr2:98290271-98290734	GM12878	blood:	n/a	n/a
22	CHD2	chr2:98289973-98290358	K562	blood:	n/a	n/a
23	CREB1	chr2:98290269-98290826	GM12878	blood:	n/a	n/a
24	CTCF	chr2:98289900-98290050	HepG2	liver:	n/a	n/a
25	CUX1	chr2:98289765-98290963	K562	blood:	n/a	n/a
26	EBF1	chr2:98290517-98290720	GM12878	blood:	n/a	n/a
27	EBF1	chr2:98290366-98290716	GM12878	blood:	n/a	n/a
28	EBF1	chr2:98293193-98293238	GM12878	blood:	n/a	n/a
29	ELF1	chr2:98289603-98289887	K562	blood:	n/a	chr2:98289697-98289710
30	ELK1	chr2:98290113-98290428	K562	blood:	n/a	n/a
31	EP300	chr2:98290314-98290744	GM12878	blood:	n/a	n/a
32	EP300	chr2:98290234-98290883	GM12878	blood:	n/a	chr2:98290829-98290836
33	EP300	chr2:98289994-98290858	K562	blood:	n/a	chr2:98290829-98290836 chr2:98290140-98290147
34	EP300	chr2:98294890-98295169	K562	blood:	n/a	n/a
35	EP300	chr2:98291506-98291706	GM12878	blood:	n/a	n/a
36	EP300	chr2:98290130-98290883	GM12878	blood:	n/a	chr2:98290829-98290836 chr2:98290140-98290147
37	FOS	chr2:98294169-98294201	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr2:98293288-98293445	MCF10A-Er-Src	breast:	n/a	chr2:98293343-98293352
39	FOS	chr2:98293966-98294357	HUVEC	blood vessel:	n/a	n/a
40	FOS	chr2:98294120-98294257	MCF10A-Er-Src	breast:	n/a	n/a
41	FOXM1	chr2:98290276-98290811	GM12878	blood:	n/a	n/a
42	GABPA	chr2:98290096-98290429	K562	blood:	n/a	n/a
43	GATA2	chr2:98289955-98290423	K562	blood:	n/a	chr2:98290267-98290276 chr2:98290258-98290275 chr2:98290267-98290277 chr2:98290265-98290278 chr2:98290269-98290276
44	HCFC1	chr2:98290150-98290481	K562	blood:	n/a	n/a
45	HDAC2	chr2:98290091-98290315	K562	blood:	n/a	chr2:98290268-98290277
46	HMGN3	chr2:98289880-98290729	K562	blood:	n/a	n/a
47	IRF1	chr2:98289378-98289569	K562	blood:	n/a	chr2:98289409-98289429 chr2:98289415-98289429 chr2:98289413-98289427 chr2:98289417-98289428 chr2:98289411-98289425
48	IRF1	chr2:98290558-98290822	K562	blood:	n/a	n/a
49	JUN	chr2:98294955-98295190	K562	blood:	n/a	n/a
50	JUND	chr2:98294860-98295116	K562	blood:	n/a	n/a

No data

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:98294916..98296768-chr2:98299787..98302603,2	K562	blood:
2	chr2:98277540..98280673-chr2:98288354..98290107,4	K562	blood:
3	chr2:98286306..98287909-chr2:98288768..98291732,2	MCF-7	breast:
4	chr2:98280058..98282999-chr2:98300256..98302493,2	MCF-7	breast:
5	chr2:98292299..98294118-chr2:98294260..98295884,2	MCF-7	breast:
6	chr2:98261851..98263583-chr2:98294061..98295719,2	K562	blood:
7	chr2:98281331..98283543-chr2:98299701..98302618,2	K562	blood:
8	chr2:98284536..98287001-chr2:98294282..98297040,2	MCF-7	breast:
9	chr2:98261015..98264268-chr2:98289158..98291782,3	K562	blood:
10	chr2:98292657..98295040-chr2:98297024..98299611,2	K562	blood:
11	chr2:98284406..98287115-chr2:98292594..98294105,2	K562	blood:
12	chr2:98292299..98294118-chr2:98294260..98295884,2	MCF-7	breast:
13	chr2:98288466..98292102-chr2:98293593..98297328,6	K562	blood:
14	chr2:98294916..98296768-chr2:98299787..98302603,2	K562	blood:
15	chr2:98292657..98295040-chr2:98297024..98299611,2	K562	blood:
16	chr2:98279513..98282179-chr2:98292256..98296228,3	MCF-7	breast:
17	chr2:98277787..98279697-chr2:98287927..98289913,2	MCF-7	breast:
18	chr2:98282003..98283543-chr2:98299701..98302691,2	K562	blood:
19	chr2:98261345..98263596-chr2:98299291..98301582,2	MCF-7	breast:
20	chr2:98279912..98282586-chr2:98290130..98292098,3	K562	blood:
21	chr2:98277609..98280060-chr2:98302722..98304227,2	MCF-7	breast:

(count:54 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZAP70-2	chr2:98290919-98291051	NONHSAT072667
2	lnc-ZAP70-2	chr2:98292094-98292184	ENSG00000228486.5
3	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
4	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
5	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
6	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
7	lnc-ZAP70-2	chr2:98292308-98292391	NR_038386
8	lnc-ZAP70-2	chr2:98293882-98294218	ENSG00000228486.5
9	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
10	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
11	lnc-ZAP70-2	chr2:98292284-98292391	ENSG00000228486.5
12	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
13	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
14	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
15	lnc-ZAP70-2	chr2:98292094-98292184	ENSG00000228486.5
16	lnc-ZAP70-2	chr2:98289635-98292184	NONHSAT072675
17	lnc-ZAP70-2	chr2:98289635-98291020	NONHSAT072676
18	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
19	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.2
20	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
21	lnc-ZAP70-2	chr2:98287806-98289283	NONHSAT072674
22	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
23	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
24	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
25	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
26	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
27	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
28	lnc-ZAP70-2	chr2:98292094-98292391	NONHSAT072676
29	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
30	lnc-ZAP70-2	chr2:98292094-98292184	NR_038386
31	lnc-ZAP70-2	chr2:98292284-98292391	ENSG00000228486.2
32	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
33	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
34	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.2
35	lnc-ZAP70-2	chr2:98290919-98291020	NR_038386
36	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
37	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
38	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.2
39	lnc-ZAP70-2	chr2:98290791-98291020	ENSG00000228486.5
40	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.2
41	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
42	lnc-ZAP70-2	chr2:98292094-98292184	ENSG00000228486.2
43	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
44	lnc-ZAP70-2	chr2:98292094-98292184	ENSG00000228486.5
45	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5
46	lnc-ZAP70-2	chr2:98292094-98292184	ENSG00000228486.5
47	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.2
48	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
49	lnc-ZAP70-2	chr2:98292308-98292391	ENSG00000228486.5
50	lnc-ZAP70-2	chr2:98290919-98291020	ENSG00000228486.5

No data

Variant related genes	Relation type
LINC01125	TF binding region
ENSG00000115073	chromatin interactions
ENSG00000135940	chromatin interactions
ENSG00000201806	chromatin interactions
ENSG00000228486	chromatin interactions

Extended variants
information (count: 480 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192254513	chr2:98289197-98289198	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs575694485	chr2:98289260-98289261	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs570699880	chr2:98289283-98289284	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs543591939	chr2:98289304-98289305	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs370866648	chr2:98289380-98289381	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs373956856	chr2:98289438-98289439	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs545790977	chr2:98289452-98289453	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs529056690	chr2:98289475-98289476	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs548837261	chr2:98289485-98289486	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs558072554	chr2:98289546-98289547	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs559236873	chr2:98289559-98289560	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs528060213	chr2:98289603-98289604	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs551118781	chr2:98289608-98289609	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs576622045	chr2:98289614-98289615	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs115130079	chr2:98289680-98289681	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs536787900	chr2:98289780-98289781	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs182830916	chr2:98289808-98289809	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs10496323	chr2:98289839-98289840	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs541153458	chr2:98289866-98289867	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs536862109	chr2:98289895-98289896	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs553670610	chr2:98289902-98289903	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs567208278	chr2:98289910-98289911	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs539029517	chr2:98289918-98289919	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs6745653	chr2:98289997-98289998	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs188402911	chr2:98290036-98290037	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs192243808	chr2:98290087-98290088	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs548053466	chr2:98290088-98290089	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs573466161	chr2:98290111-98290112	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs542446823	chr2:98290152-98290153	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs559201603	chr2:98290182-98290183	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs551353212	chr2:98290210-98290211	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
32	rs544981240	chr2:98290221-98290222	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs564685623	chr2:98290236-98290237	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs530534340	chr2:98290419-98290420	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs550379416	chr2:98290428-98290429	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs567387556	chr2:98290451-98290452	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs149266632	chr2:98290452-98290453	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs184681557	chr2:98290493-98290494	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs376151269	chr2:98290533-98290534	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
40	rs538920494	chr2:98290579-98290580	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs189295504	chr2:98290612-98290613	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
42	rs144502871	chr2:98290674-98290675	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
43	rs538253989	chr2:98290710-98290711	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs57183691	chr2:98290724-98290725	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs562900284	chr2:98290764-98290765	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
46	rs192325986	chr2:98290789-98290790	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
47	rs574619460	chr2:98290792-98290793	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
48	rs184714674	chr2:98290857-98290858	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
49	rs72493444	chr2:98290861-98290862	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76108604	chr2:98290867-98290868	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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	17483303	CNVD
Medulloblastoma	20607354	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
Ovarian cancer	21781307	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98281000-98290400	Weak transcription	Spleen	Spleen
2	chr2:98281000-98323800	Weak transcription	Gastric	stomach
3	chr2:98281200-98289600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr2:98281400-98289400	Weak transcription	Lung	lung
5	chr2:98281400-98290000	Weak transcription	Left Ventricle	heart
6	chr2:98281400-98295200	Weak transcription	Esophagus	oesophagus
7	chr2:98281600-98289600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:98281600-98289600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr2:98281600-98289800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:98281600-98290000	Weak transcription	Fetal Intestine Small	intestine
11	chr2:98281600-98290200	Weak transcription	Pancreas	Pancrea
12	chr2:98281600-98290400	Weak transcription	Thymus	Thymus
13	chr2:98281600-98291400	Weak transcription	Right Atrium	heart
14	chr2:98281600-98292000	Weak transcription	Adipose Nuclei	Adipose
15	chr2:98281600-98292800	Weak transcription	HSMM	muscle
16	chr2:98281600-98293200	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr2:98281600-98294800	Weak transcription	Brain Anterior Caudate	brain
18	chr2:98281600-98295400	Weak transcription	Right Ventricle	heart
19	chr2:98281600-98298800	Weak transcription	Aorta	Aorta
20	chr2:98281800-98289200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr2:98281800-98289600	Weak transcription	GM12878-XiMat	blood
22	chr2:98281800-98293800	Weak transcription	Brain Angular Gyrus	brain
23	chr2:98281800-98296200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:98281800-98296200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr2:98282000-98290000	Weak transcription	Brain Hippocampus Middle	brain
26	chr2:98282000-98292000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:98282000-98293800	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr2:98285600-98292200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr2:98286200-98292000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:98286400-98289600	Weak transcription	Fetal Stomach	stomach
31	chr2:98286400-98289800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:98288400-98289600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr2:98288600-98293600	Weak transcription	Fetal Muscle Leg	muscle
34	chr2:98289000-98289800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:98289200-98289800	Enhancers	K562	blood
36	chr2:98289200-98290000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:98289200-98291600	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr2:98289200-98292000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr2:98289400-98290400	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr2:98289400-98292200	Enhancers	Primary hematopoietic stem cells	blood
41	chr2:98289600-98289800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr2:98289600-98290000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr2:98289600-98290400	Enhancers	Fetal Thymus	thymus
44	chr2:98289600-98290400	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr2:98289600-98291600	Enhancers	GM12878-XiMat	blood
46	chr2:98289800-98290600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr2:98289800-98291000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:98289800-98291000	Flanking Active TSS	K562	blood
49	chr2:98289800-98293600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:98290000-98290200	Enhancers	Fetal Intestine Small	intestine

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