Variant report

Variant	nsv975603
Chromosome Location	chr12:1611168-1616803
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:41)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:41 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:1612100-1612250	GM12872	blood:	n/a	n/a
2	CTCF	chr12:1614982-1615003	HepG2	liver:	n/a	n/a
3	CTCF	chr12:1612100-1612250	BJ	skin:	n/a	n/a
4	CTCF	chr12:1612040-1612190	GM12864	blood:	n/a	n/a
5	CTCF	chr12:1612107-1612222	MCF-7	breast:	n/a	n/a
6	CTCF	chr12:1612080-1612230	AG09309	skin:	n/a	n/a
7	CTCF	chr12:1612160-1612310	AG09319	gingival:	n/a	n/a
8	CTCF	chr12:1613238-1613339	GM10248	blood:	n/a	n/a
9	CTCF	chr12:1612100-1612250	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr12:1612080-1612230	A549	lung:	n/a	n/a
11	CTCF	chr12:1611980-1612130	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr12:1612120-1612270	HRPEpiC	eye:	n/a	n/a
13	CTCF	chr12:1612080-1612230	AG10803	skin:	n/a	n/a
14	CTCF	chr12:1612120-1612270	AG10803	skin:	n/a	n/a
15	CTCF	chr12:1612060-1612210	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr12:1612060-1612210	GM12872	blood:	n/a	n/a
17	CTCF	chr12:1612080-1612230	AG09319	gingival:	n/a	n/a
18	CTCF	chr12:1612140-1612290	GM12866	blood:	n/a	n/a
19	CTCF	chr12:1612040-1612190	SAEC	small airway:	n/a	n/a
20	CTCF	chr12:1612140-1612290	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr12:1612060-1612210	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr12:1612448-1612608	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr12:1612122-1612204	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:1614881-1615014	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr12:1614900-1615050	HepG2	liver:	n/a	n/a
26	CTCF	chr12:1612082-1612233	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr12:1614800-1615044	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr12:1614879-1615117	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr12:1612380-1612530	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr12:1611840-1611990	HRPEpiC	eye:	n/a	n/a
31	KAP1	chr12:1610885-1611272	K562	blood:	n/a	n/a
32	POLR2A	chr12:1611101-1611469	K562	blood:	n/a	n/a
33	POLR2A	chr12:1616245-1616294	GM12878	blood:	n/a	n/a
34	POLR2A	chr12:1616217-1616241	GM12878	blood:	n/a	n/a
35	RAD21	chr12:1614718-1615145	H1-hESC	embryonic stem cell:	n/a	n/a
36	RAD21	chr12:1611982-1612257	H1-hESC	embryonic stem cell:	n/a	n/a
37	RAD21	chr12:1614835-1615045	H1-hESC	embryonic stem cell:	n/a	n/a
38	RAD21	chr12:1614858-1615058	H1-hESC	embryonic stem cell:	n/a	n/a
39	RAD21	chr12:1611923-1612655	H1-hESC	embryonic stem cell:	n/a	n/a
40	SPI1	chr12:1613380-1613887	HL-60	blood:	n/a	chr12:1613643-1613652 chr12:1613641-1613654
41	ZEB1	chr12:1613807-1613987	GM12878	blood:	n/a	chr12:1613881-1613890 chr12:1613852-1613861

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1614439-1614489	HL-60	blood:	n/a
2	chr12:1614439-1614489	MCF10A-Er-Src	breast:	n/a
3	chr12:1614380-1614430	ECC-1	luminal epithelium:	n/a
4	chr12:1614380-1614430	NB4	blood:	n/a
5	chr12:1614439-1614489	HRPEpiC	eye:	n/a
6	chr12:1614380-1614430	AG04449	skin:	fetal
7	chr12:1612664-1612714	GM12892	blood:	n/a
8	chr12:1612672-1612722	Caco-2	colon:	n/a
9	chr12:1614439-1614489	AG04449	skin:	fetal
10	chr12:1614380-1614430	NH-A	brain:	n/a
11	chr12:1612770-1612820	SKMC	muscle:	n/a
12	chr12:1614380-1614430	U87	brain:	n/a
13	chr12:1612664-1612714	HMEC	breast:	n/a
14	chr12:1612664-1612714	SK-N-SH	brain:	n/a
15	chr12:1614439-1614489	GM12878	blood:	n/a
16	chr12:1612770-1612820	H1-hESC	embryonic stem cell:	embryo
17	chr12:1612664-1612714	HEK293	kidney:	embryo
18	chr12:1614380-1614430	NHDF-neo	bronchial:	n/a
19	chr12:1614380-1614430	PrEC	prostate:	n/a
20	chr12:1612672-1612722	IMR90	lung:	fetal
21	chr12:1612664-1612714	NB4	blood:	n/a
22	chr12:1612664-1612714	HRPEpiC	eye:	n/a
23	chr12:1612770-1612820	HEK293	kidney:	embryo
24	chr12:1612672-1612722	HRE	kidney:	n/a
25	chr12:1612664-1612714	NT2-D1	testis:	n/a
26	chr12:1614380-1614430	HCPEpiC	choroid plexus:	n/a
27	chr12:1614380-1614430	HCF	heart:	n/a
28	chr12:1614380-1614430	GM12878	blood:	n/a
29	chr12:1614380-1614430	HIPEpiC	eye:	n/a
30	chr12:1612664-1612714	Jurkat	blood:	n/a
31	chr12:1614439-1614489	SK-N-MC	brain:	n/a
32	chr12:1614439-1614489	HCF	heart:	n/a
33	chr12:1614439-1614489	PrEC	prostate:	n/a
34	chr12:1614380-1614430	ovcar-3	ovarian:	n/a
35	chr12:1614380-1614430	CMK	blood:	n/a
36	chr12:1612664-1612714	HRE	kidney:	n/a
37	chr12:1612770-1612820	RPTEC	kidney:	n/a
38	chr12:1614380-1614430	AG09319	gingival:	n/a
39	chr12:1612770-1612820	HEEpiC	esophagus:	n/a
40	chr12:1614439-1614489	CMK	blood:	n/a
41	chr12:1614439-1614489	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:1612770-1612820	NT2-D1	testis:	n/a
43	chr12:1612770-1612820	Jurkat	blood:	n/a
44	chr12:1612664-1612714	Hepatocyte	liver:	n/a
45	chr12:1614380-1614430	AG10803	skin:	n/a
46	chr12:1612672-1612722	RPTEC	kidney:	n/a
47	chr12:1612770-1612820	HUVEC	blood vessel:	n/a
48	chr12:1612770-1612820	HRCEpiC	kidney:	n/a
49	chr12:1614439-1614489	HIPEpiC	eye:	n/a
50	chr12:1612672-1612722	HCT-116	colon:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:1603741..1607368-chr12:1607408..1611728,5	K562	blood:
2	chr12:1609960..1612455-chr12:1612690..1615017,2	K562	blood:
3	chr12:1603741..1607368-chr12:1607408..1611542,6	K562	blood:
4	chr12:1611483..1613501-chr12:1625253..1627123,2	K562	blood:
5	chr12:1609960..1612455-chr12:1612690..1615017,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERC1-1	chr12:1611627-1612636	ENSG00000249628
2	lnc-ERC1-1	chr12:1611633-1613590	XLOC_009615
3	lnc-ERC1-1	chr12:1615336-1616484	NONHSAT025400
4	lnc-ERC1-1	chr12:1611633-1612648	ENSG00000249628
5	lnc-ERC1-1	chr12:1611633-1612648	XLOC_009615
6	lnc-ERC1-1	chr12:1612440-1613590	NONHSAT025399
7	lnc-ERC1-1	chr12:1615339-1616484	XLOC_009615
8	lnc-FBXL14-1	chr12:1611627-1612636	ENSG00000249628
9	lnc-ERC1-1	chr12:1615339-1616484	ENSG00000249628
10	lnc-FBXL14-1	chr12:1615325-1616484	ENSG00000249628
11	lnc-ERC1-1	chr12:1615325-1616484	ENSG00000249628

No data

Variant related genes	Relation type
LINC00942	TF binding region
LINC00942	CpG island
RNMT	miRNA target sites
ATP8A2	miRNA target sites
PDCD10	miRNA target sites
PTPRK	miRNA target sites
PRPF4B	miRNA target sites

Extended variants
information (count: 295 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560544445	chr12:1611229-1611230	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs527555792	chr12:1611233-1611234	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs184596272	chr12:1611236-1611237	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs74057825	chr12:1611266-1611267	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs531516862	chr12:1611272-1611273	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs144897413	chr12:1611279-1611280	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs568942818	chr12:1611292-1611293	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs538739894	chr12:1611294-1611295	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs529928404	chr12:1611323-1611324	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs190343288	chr12:1611340-1611341	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs7311422	chr12:1611356-1611357	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs566272476	chr12:1611369-1611370	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs534199915	chr12:1611384-1611385	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs556003457	chr12:1611394-1611395	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs576746171	chr12:1611416-1611417	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs138743174	chr12:1611438-1611439	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs538041770	chr12:1611439-1611440	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs556389876	chr12:1611474-1611475	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs141775646	chr12:1611554-1611555	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs113617449	chr12:1611566-1611567	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs11061787	chr12:1611571-1611572	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572381657	chr12:1611581-1611582	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs146238274	chr12:1611607-1611608	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs552373956	chr12:1611615-1611616	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs375753976	chr12:1611618-1611619	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs559981296	chr12:1611665-1611666	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
27	rs551761800	chr12:1611666-1611667	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
28	rs115574048	chr12:1611716-1611717	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
29	rs367546573	chr12:1611722-1611723	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
30	rs367958154	chr12:1611743-1611744	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
31	rs561154649	chr12:1611758-1611759	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
32	rs531684116	chr12:1611773-1611774	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
33	rs140841227	chr12:1611799-1611800	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
34	rs139305320	chr12:1611800-1611801	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
35	rs34366431	chr12:1611801-1611802	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
36	rs149806500	chr12:1611814-1611815	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
37	rs60096705	chr12:1611824-1611825	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
38	rs565083462	chr12:1611842-1611843	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
39	rs4765821	chr12:1611846-1611847	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs181675950	chr12:1611859-1611860	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
41	rs138001980	chr12:1611881-1611882	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
42	rs4765822	chr12:1611894-1611895	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs547920574	chr12:1611964-1611965	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
44	rs567619291	chr12:1612007-1612008	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
45	rs575725253	chr12:1612012-1612013	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
46	rs77790501	chr12:1612036-1612037	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
47	rs556299823	chr12:1612054-1612055	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
48	rs186724173	chr12:1612055-1612056	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
49	rs538887869	chr12:1612075-1612076	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
50	rs554221246	chr12:1612076-1612077	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1600800-1612600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr12:1600800-1613600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr12:1602200-1611400	Weak transcription	Fetal Brain Female	brain
4	chr12:1602200-1613800	Weak transcription	Primary B cells from cord blood	blood
5	chr12:1603400-1611400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr12:1603600-1611200	Weak transcription	Brain Germinal Matrix	brain
7	chr12:1604800-1613400	Weak transcription	Primary T cells from cord blood	blood
8	chr12:1605000-1611600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:1605000-1611800	Weak transcription	Fetal Intestine Small	intestine
10	chr12:1606000-1611200	Weak transcription	Colonic Mucosa	Colon
11	chr12:1606000-1611200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr12:1606200-1611400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr12:1606200-1611800	Weak transcription	NHEK	skin
14	chr12:1607200-1611800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr12:1607200-1613800	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr12:1607400-1611200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:1608400-1613000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr12:1608800-1618600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:1609200-1611200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr12:1609400-1611600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:1609400-1612200	Enhancers	Fetal Muscle Leg	muscle
22	chr12:1609600-1611800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:1609600-1613400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:1609800-1611400	Weak transcription	Brain Anterior Caudate	brain
25	chr12:1609800-1612400	Weak transcription	Esophagus	oesophagus
26	chr12:1609800-1613400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr12:1609800-1613600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:1610000-1611200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:1610000-1611600	Weak transcription	Fetal Brain Male	brain
30	chr12:1610000-1611800	Enhancers	HSMM	muscle
31	chr12:1610000-1612400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr12:1610000-1613800	Weak transcription	Placenta	Placenta
33	chr12:1610200-1611200	Weak transcription	NHDF-Ad	bronchial
34	chr12:1610200-1611200	Weak transcription	NHLF	lung
35	chr12:1610200-1612200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr12:1610200-1612400	Enhancers	Adipose Nuclei	Adipose
37	chr12:1610200-1613000	Enhancers	HSMMtube	muscle
38	chr12:1610400-1615000	Weak transcription	K562	blood
39	chr12:1610600-1612000	Enhancers	Brain Substantia Nigra	brain
40	chr12:1610800-1611200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr12:1610800-1611200	ZNF genes & repeats	Fetal Stomach	stomach
42	chr12:1610800-1611200	ZNF genes & repeats	Spleen	Spleen
43	chr12:1610800-1611800	Enhancers	Stomach Smooth Muscle	stomach
44	chr12:1610800-1612800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr12:1611000-1611400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr12:1611000-1611600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr12:1611000-1611800	Enhancers	Colon Smooth Muscle	Colon
48	chr12:1611000-1612400	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr12:1611000-1612400	Enhancers	Fetal Lung	lung
50	chr12:1611000-1612400	Enhancers	A549	lung

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