Variant report

Variant	esv3338485
Chromosome Location	chr2:99347070-99348418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:99347710-99347908	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:99348284-99349093	HepG2	liver:	n/a	n/a
3	BACH1	chr2:99347838-99348187	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr2:99347751-99348118	GM12878	blood:	n/a	chr2:99348042-99348058
5	BRCA1	chr2:99347882-99347930	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:99347750-99347916	HepG2	liver:	n/a	n/a
7	CCNT2	chr2:99347175-99347456	K562	blood:	n/a	n/a
8	CEBPB	chr2:99348249-99348809	HepG2	liver:	n/a	n/a
9	CEBPD	chr2:99347639-99347979	HepG2	liver:	n/a	n/a
10	CEBPD	chr2:99346652-99347301	HepG2	liver:	n/a	n/a
11	CEBPD	chr2:99347647-99347927	HepG2	liver:	n/a	n/a
12	CHD1	chr2:99348067-99348246	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr2:99347958-99347989	GM12878	blood:	n/a	n/a
14	CHD2	chr2:99347720-99348370	HepG2	liver:	n/a	n/a
15	CHD2	chr2:99347694-99348352	GM12878	blood:	n/a	n/a
16	CHD2	chr2:99347101-99347164	HepG2	liver:	n/a	n/a
17	CREB1	chr2:99346553-99348804	HepG2	liver:	n/a	n/a
18	CREB1	chr2:99347648-99348058	A549	lung:	n/a	n/a
19	CTCF	chr2:99347315-99347451	Kidney_OC	kidney:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
20	CTCF	chr2:99347280-99347430	HAc	cerebellar:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
21	CTCF	chr2:99347341-99347410	Lung_OC	lung:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
22	CTCF	chr2:99347296-99347446	A549	lung:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
23	CTCF	chr2:99347280-99347430	GM12873	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
24	CTCF	chr2:99347280-99347430	HRPEpiC	eye:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
25	CTCF	chr2:99347330-99347336	NHEK	skin:	n/a	n/a
26	CTCF	chr2:99347300-99347450	GM12866	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
27	CTCF	chr2:99347226-99347431	HepG2	liver:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
28	CTCF	chr2:99347240-99347390	BJ	skin:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
29	CTCF	chr2:99347300-99347450	GM06990	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
30	CTCF	chr2:99347280-99347430	GM12871	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
31	CTCF	chr2:99347337-99347426	NHEK	skin:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
32	CTCF	chr2:99347287-99347438	LNCaP	prostate:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
33	CTCF	chr2:99347240-99347390	GM12872	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
34	CTCF	chr2:99347260-99347410	GM12878	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
35	CTCF	chr2:99347321-99347390	MCF-7	breast:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
36	CTCF	chr2:99347330-99347388	LNCaP	prostate:	n/a	chr2:99347374-99347382
37	CTCF	chr2:99347325-99347365	GM10248	blood:	n/a	n/a
38	CTCF	chr2:99347220-99347370	HMEC	breast:	n/a	n/a
39	CTCF	chr2:99347340-99347490	GM12874	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
40	CTCF	chr2:99347300-99347450	GM12865	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
41	CTCF	chr2:99347240-99347390	HRPEpiC	eye:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
42	CTCF	chr2:99347322-99347416	IMR90	lung:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
43	CTCF	chr2:99347260-99347410	Caco-2	colon:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
44	CTCF	chr2:99347273-99347400	SK-N-SH_RA	brain:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
45	CTCF	chr2:99346940-99347090	GM12868	blood:	n/a	n/a
46	CTCF	chr2:99347230-99347495	K562	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
47	CTCF	chr2:99347240-99347390	HPF	lung:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
48	CTCF	chr2:99347300-99347450	GM12867	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
49	CTCF	chr2:99347300-99347450	HCT-116	colon:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
50	CTCF	chr2:99347280-99347430	GM12866	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99347422-99347472	HMEC	breast:	n/a
2	chr2:99348232-99348282	NT2-D1	testis:	n/a
3	chr2:99347422-99347472	HEEpiC	esophagus:	n/a
4	chr2:99347987-99348037	HEEpiC	esophagus:	n/a
5	chr2:99347987-99348037	GM19239	blood:	n/a
6	chr2:99347854-99347904	H1-hESC	embryonic stem cell:	embryo
7	chr2:99347854-99347904	AG04450	lung:	fetal
8	chr2:99347987-99348037	SK-N-MC	brain:	n/a
9	chr2:99347422-99347472	IMR90	lung:	fetal
10	chr2:99347979-99348029	MCF-7	breast:	n/a
11	chr2:99348176-99348226	BE2_C	brain:	n/a
12	chr2:99348232-99348282	MCF10A-Er-Src	breast:	n/a
13	chr2:99347987-99348037	CMK	blood:	n/a
14	chr2:99347979-99348029	RPTEC	kidney:	n/a
15	chr2:99347987-99348037	LNCaP	prostate:	n/a
16	chr2:99347979-99348029	SK-N-SH	brain:	n/a
17	chr2:99348176-99348226	K562	blood:	n/a
18	chr2:99348176-99348226	GM12891	blood:	n/a
19	chr2:99347422-99347472	ECC-1	luminal epithelium:	n/a
20	chr2:99348232-99348282	SKMC	muscle:	n/a
21	chr2:99348176-99348226	HRPEpiC	eye:	n/a
22	chr2:99347854-99347904	RPTEC	kidney:	n/a
23	chr2:99347979-99348029	MCF10A-Er-Src	breast:	n/a
24	chr2:99347422-99347472	AoSMC	blood vessel:	n/a
25	chr2:99347854-99347904	Hepatocyte	liver:	n/a
26	chr2:99347987-99348037	HMEC	breast:	n/a
27	chr2:99348232-99348282	HIPEpiC	eye:	n/a
28	chr2:99347979-99348029	AG04450	lung:	fetal
29	chr2:99347854-99347904	NT2-D1	testis:	n/a
30	chr2:99348176-99348226	PrEC	prostate:	n/a
31	chr2:99347422-99347472	Hepatocyte	liver:	n/a
32	chr2:99348232-99348282	ovcar-3	ovarian:	n/a
33	chr2:99347987-99348037	HCPEpiC	choroid plexus:	n/a
34	chr2:99348232-99348282	Hela-S3	cervix:	n/a
35	chr2:99348232-99348282	RPTEC	kidney:	n/a
36	chr2:99347422-99347472	NH-A	brain:	n/a
37	chr2:99347979-99348029	GM12892	blood:	n/a
38	chr2:99347854-99347904	IMR90	lung:	fetal
39	chr2:99347854-99347904	HEK293	kidney:	embryo
40	chr2:99347987-99348037	HepG2	liver:	n/a
41	chr2:99347422-99347472	SK-N-SH_RA	brain:	n/a
42	chr2:99348176-99348226	HCM	heart:	n/a
43	chr2:99347979-99348029	HNPCEpiC	eye:	n/a
44	chr2:99348176-99348226	HCF	heart:	n/a
45	chr2:99347422-99347472	HCT-116	colon:	n/a
46	chr2:99347422-99347472	NHBE	bronchial:	n/a
47	chr2:99347854-99347904	ovcar-3	ovarian:	n/a
48	chr2:99347987-99348037	SK-N-SH	brain:	n/a
49	chr2:99347422-99347472	SAEC	small airway:	n/a
50	chr2:99347422-99347472	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:99336480..99339286-chr2:99347871..99349769,2	MCF-7	breast:
2	chr2:99342514..99344879-chr2:99346177..99348798,2	K562	blood:
3	chr2:99345360..99347894-chr2:99396622..99399352,2	MCF-7	breast:
4	chr2:99221557..99223102-chr2:99346482..99348239,2	MCF-7	breast:
5	chr2:99345368..99349321-chr2:99385005..99390572,6	MCF-7	breast:
6	chr2:99342228..99344879-chr2:99346177..99348874,2	K562	blood:
7	chr2:99344922..99348721-chr2:99382903..99389092,6	MCF-7	breast:
8	chr2:99348346..99350092-chr2:99446085..99447956,2	MCF-7	breast:
9	chr2:99343338..99345259-chr2:99346373..99348700,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC50-1	chr2:99347828-99348158	NONHSAT072721
2	lnc-UNC50-1	chr2:99348118-99348158	XLOC_001587

Variant related genes	Relation type
MGAT4A	TF binding region
MGAT4A	CpG island
ENSG00000071073	chromatin interactions
ENSG00000226791	chromatin interactions
ENSG00000201070	chromatin interactions
ENSG00000183513	chromatin interactions

Extended variants
information (count: 35 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541957490	chr2:99347084-99347085	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs555574282	chr2:99347181-99347182	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs185816156	chr2:99347197-99347198	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs572429905	chr2:99347200-99347201	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs34841901	chr2:99347210-99347211	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs190236428	chr2:99347240-99347241	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs560411925	chr2:99347348-99347349	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs532418149	chr2:99347507-99347508	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs546023815	chr2:99347509-99347510	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs559389584	chr2:99347563-99347564	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs562632243	chr2:99347698-99347699	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs5008045	chr2:99347699-99347700	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs369385191	chr2:99347724-99347725	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs568042354	chr2:99347757-99347758	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs527317674	chr2:99347758-99347759	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs547045548	chr2:99347846-99347847	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
17	rs570833849	chr2:99347861-99347862	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs373393595	chr2:99347879-99347880	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs556350722	chr2:99347905-99347906	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs7420869	chr2:99347917-99347918	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs369165851	chr2:99347920-99347921	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs141803663	chr2:99347943-99347944	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs528302020	chr2:99347992-99347993	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs555862268	chr2:99348114-99348115	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs537930306	chr2:99348151-99348152	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs572413384	chr2:99348152-99348153	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs541437417	chr2:99348161-99348162	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs557819636	chr2:99348209-99348210	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs185679578	chr2:99348216-99348217	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs546159755	chr2:99348239-99348240	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs562768468	chr2:99348266-99348267	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs541459569	chr2:99348291-99348292	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs111408008	chr2:99348320-99348321	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs376530906	chr2:99348335-99348336	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs541645181	chr2:99348402-99348403	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 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
T-cell prolymphocytic leukemia	17713554	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99344200-99348400	Active TSS	Primary T cells fromperipheralblood	blood
2	chr2:99344600-99348600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr2:99344800-99348600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
4	chr2:99345000-99348800	Active TSS	Duodenum Mucosa	Duodenum
5	chr2:99345200-99348400	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr2:99345400-99348400	Active TSS	Primary T cells from cord blood	blood
7	chr2:99345600-99348400	Active TSS	Primary T helper cells PMA-I stimulated	--
8	chr2:99345600-99348400	Active TSS	Fetal Intestine Large	intestine
9	chr2:99345600-99349200	Active TSS	Colonic Mucosa	Colon
10	chr2:99345800-99348200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
11	chr2:99345800-99348200	Active TSS	Brain Anterior Caudate	brain
12	chr2:99345800-99348200	Active TSS	Stomach Smooth Muscle	stomach
13	chr2:99345800-99348400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
14	chr2:99345800-99348400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
15	chr2:99345800-99348400	Active TSS	Ovary	ovary
16	chr2:99345800-99348400	Active TSS	Psoas Muscle	Psoas
17	chr2:99345800-99348400	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr2:99345800-99348400	Active TSS	Sigmoid Colon	Sigmoid Colon
19	chr2:99345800-99348400	Active TSS	Small Intestine	intestine
20	chr2:99345800-99348600	Active TSS	Right Atrium	heart
21	chr2:99345800-99348800	Active TSS	Duodenum Smooth Muscle	Duodenum
22	chr2:99345800-99348800	Active TSS	Fetal Intestine Small	intestine
23	chr2:99345800-99348800	Active TSS	Right Ventricle	heart
24	chr2:99345800-99349400	Active TSS	Pancreas	Pancrea
25	chr2:99346000-99348200	Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr2:99346000-99348400	Active TSS	Brain Hippocampus Middle	brain
27	chr2:99346000-99348400	Active TSS	Brain Substantia Nigra	brain
28	chr2:99346000-99348600	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr2:99346000-99348600	Bivalent/Poised TSS	HepG2	liver
30	chr2:99346200-99348200	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr2:99346200-99348400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
32	chr2:99346200-99348600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr2:99346200-99348600	Active TSS	Aorta	Aorta
34	chr2:99346200-99348800	Active TSS	Left Ventricle	heart
35	chr2:99346200-99348800	Active TSS	Lung	lung
36	chr2:99346200-99348800	Active TSS	Thymus	Thymus
37	chr2:99346400-99348200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
38	chr2:99346400-99348200	Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr2:99346400-99348200	Active TSS	Brain Cingulate Gyrus	brain
40	chr2:99346400-99348200	Active TSS	Stomach Mucosa	stomach
41	chr2:99346400-99348400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:99346400-99348400	Active TSS	Brain Angular Gyrus	brain
43	chr2:99346400-99348600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr2:99346400-99348600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
45	chr2:99346600-99347200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
46	chr2:99346600-99347200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr2:99346600-99347200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:99346600-99347200	Active TSS	Fetal Kidney	kidney
49	chr2:99346600-99347200	Bivalent/Poised TSS	HSMMtube	muscle
50	chr2:99346600-99348000	Active TSS	Primary T regulatory cells fromperipheralblood	blood

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