Variant report

Variant	esv1795347
Chromosome Location	chr12:29458556-29471835
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	chr12:29470763-29471106	K562	blood:	n/a	n/a
2	ARID3A	chr12:29470763-29471089	HepG2	liver:	n/a	n/a
3	ATF1	chr12:29470766-29471083	K562	blood:	n/a	n/a
4	BHLHE40	chr12:29470552-29471099	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:29470724-29471094	K562	blood:	n/a	n/a
6	BRCA1	chr12:29470761-29471060	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:29470724-29471090	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:29470698-29471088	MCF-7	breast:	n/a	n/a
9	CEBPB	chr12:29470717-29471047	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr12:29462340-29462490	HMEC	breast:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
11	CTCF	chr12:29470820-29470970	HEEpiC	esophagus:	n/a	chr12:29470852-29470870
12	CTCF	chr12:29470820-29470970	GM12866	blood:	n/a	chr12:29470852-29470870
13	CTCF	chr12:29470760-29470910	WI-38	lung:	n/a	chr12:29470852-29470870
14	CTCF	chr12:29470840-29470990	GM12872	blood:	n/a	chr12:29470852-29470870
15	CTCF	chr12:29470638-29471133	GM12878	blood:	n/a	chr12:29470852-29470870
16	CTCF	chr12:29462379-29462511	GM10248	blood:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
17	CTCF	chr12:29462580-29462730	GM12872	blood:	n/a	n/a
18	CTCF	chr12:29470800-29470950	AoAF	blood vessel:	n/a	chr12:29470852-29470870
19	CTCF	chr12:29462440-29462590	HVMF	connective:	n/a	chr12:29462440-29462461 chr12:29462441-29462454
20	CTCF	chr12:29470820-29470970	WERI-Rb-1	eye:	n/a	chr12:29470852-29470870
21	CTCF	chr12:29462364-29462533	Spleen_OC	spleen:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
22	CTCF	chr12:29470800-29470950	AG10803	skin:	n/a	chr12:29470852-29470870
23	CTCF	chr12:29470800-29470950	HCT-116	colon:	n/a	chr12:29470852-29470870
24	CTCF	chr12:29462320-29462470	Caco-2	colon:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
25	CTCF	chr12:29462327-29462556	K562	blood:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
26	CTCF	chr12:29470840-29470990	AG09309	skin:	n/a	chr12:29470852-29470870
27	CTCF	chr12:29470725-29471069	Lung_OC	lung:	n/a	chr12:29470852-29470870
28	CTCF	chr12:29470800-29470950	GM12872	blood:	n/a	chr12:29470852-29470870
29	CTCF	chr12:29470820-29470970	SK-N-SH_RA	brain:	n/a	chr12:29470852-29470870
30	CTCF	chr12:29470448-29471228	A549	lung:	n/a	chr12:29470852-29470870
31	CTCF	chr12:29470762-29471058	GM13977	blood:	n/a	chr12:29470852-29470870
32	CTCF	chr12:29470840-29470990	HA-sp	spinal cord:	n/a	chr12:29470852-29470870
33	CTCF	chr12:29470840-29470990	GM12801	blood:	n/a	chr12:29470852-29470870
34	CTCF	chr12:29470840-29470990	Caco-2	colon:	n/a	chr12:29470852-29470870
35	CTCF	chr12:29470744-29471059	LNCaP	prostate:	n/a	chr12:29470852-29470870
36	CTCF	chr12:29470623-29471085	H1-hESC	embryonic stem cell:	n/a	chr12:29470852-29470870
37	CTCF	chr12:29462340-29462490	GM12874	blood:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
38	CTCF	chr12:29462340-29462490	AG10803	skin:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
39	CTCF	chr12:29470828-29470987	H1-hESC	embryonic stem cell:	n/a	chr12:29470852-29470870
40	CTCF	chr12:29462357-29462534	K562	blood:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
41	CTCF	chr12:29470592-29471195	K562	blood:	n/a	chr12:29470852-29470870
42	CTCF	chr12:29470820-29470970	GM12873	blood:	n/a	chr12:29470852-29470870
43	CTCF	chr12:29470800-29470950	HBMEC	blood vessel:	n/a	chr12:29470852-29470870
44	CTCF	chr12:29470800-29470950	GM12866	blood:	n/a	chr12:29470852-29470870
45	CTCF	chr12:29462357-29462531	LNCaP	prostate:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
46	CTCF	chr12:29470840-29470990	NHEK	skin:	n/a	chr12:29470852-29470870
47	CTCF	chr12:29462306-29462565	A549	lung:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
48	CTCF	chr12:29462340-29462490	AoAF	blood vessel:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
49	CTCF	chr12:29462400-29462550	GM12878	blood:	n/a	chr12:29462440-29462461 chr12:29462441-29462454 chr12:29462438-29462456
50	CTCF	chr12:29470800-29470950	HA-sp	spinal cord:	n/a	chr12:29470852-29470870

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:29470962-29471012	SK-N-SH	brain:	n/a
2	chr12:29470962-29471012	T-47D	breast:	n/a
3	chr12:29470962-29471012	HEK293	kidney:	embryo
4	chr12:29470962-29471012	NHBE	bronchial:	n/a
5	chr12:29470962-29471012	HRPEpiC	eye:	n/a
6	chr12:29470962-29471012	HUVEC	blood vessel:	n/a
7	chr12:29470962-29471012	PANC-1	pancreas:	n/a
8	chr12:29470962-29471012	HCT-116	colon:	n/a
9	chr12:29470962-29471012	Hela-S3	cervix:	n/a
10	chr12:29470962-29471012	A549	lung:	n/a
11	chr12:29470962-29471012	HepG2	liver:	n/a
12	chr12:29470962-29471012	MCF-7	breast:	n/a
13	chr12:29470962-29471012	NT2-D1	testis:	n/a
14	chr12:29470962-29471012	U87	brain:	n/a
15	chr12:29470962-29471012	HMEC	breast:	n/a
16	chr12:29470962-29471012	LNCaP	prostate:	n/a
17	chr12:29470962-29471012	AG04450	lung:	fetal
18	chr12:29470962-29471012	AG09309	skin:	n/a
19	chr12:29470962-29471012	SK-N-SH_RA	brain:	n/a
20	chr12:29470962-29471012	H1-hESC	embryonic stem cell:	embryo
21	chr12:29470962-29471012	HCF	heart:	n/a
22	chr12:29470962-29471012	HCM	heart:	n/a
23	chr12:29470962-29471012	GM19239	blood:	n/a
24	chr12:29470962-29471012	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:29470962-29471012	NB4	blood:	n/a
26	chr12:29470962-29471012	SK-N-MC	brain:	n/a
27	chr12:29470962-29471012	Jurkat	blood:	n/a
28	chr12:29470962-29471012	GM12891	blood:	n/a
29	chr12:29470962-29471012	HL-60	blood:	n/a
30	chr12:29470962-29471012	PFSK-1	brain:	n/a
31	chr12:29470962-29471012	HNPCEpiC	eye:	n/a
32	chr12:29470962-29471012	GM12892	blood:	n/a
33	chr12:29470962-29471012	GM12878	blood:	n/a
34	chr12:29470962-29471012	ovcar-3	ovarian:	n/a
35	chr12:29470962-29471012	AG10803	skin:	n/a
36	chr12:29470962-29471012	NH-A	brain:	n/a
37	chr12:29470962-29471012	HCPEpiC	choroid plexus:	n/a
38	chr12:29470962-29471012	RPTEC	kidney:	n/a
39	chr12:29470962-29471012	HIPEpiC	eye:	n/a
40	chr12:29470962-29471012	Hepatocyte	liver:	n/a
41	chr12:29470962-29471012	IMR90	lung:	fetal
42	chr12:29470962-29471012	SKMC	muscle:	n/a
43	chr12:29470962-29471012	HEEpiC	esophagus:	n/a
44	chr12:29470962-29471012	SAEC	small airway:	n/a
45	chr12:29470962-29471012	PrEC	prostate:	n/a
46	chr12:29470962-29471012	NHDF-neo	bronchial:	n/a
47	chr12:29470962-29471012	GM06990	blood:	n/a
48	chr12:29470962-29471012	HRCEpiC	kidney:	n/a
49	chr12:29470962-29471012	Caco-2	colon:	n/a
50	chr12:29470962-29471012	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:29462295..29465782-chr12:29467175..29469867,4	K562	blood:
2	chr12:29462295..29464942-chr12:29467954..29469867,2	K562	blood:
3	chr12:29462346..29462982-chr12:29670343..29670928,2	K562	blood:
4	chr12:29462295..29465782-chr12:29467175..29469867,4	K562	blood:
5	chr12:29458406..29460957-chr12:29462899..29465425,2	K562	blood:
6	chr12:29462295..29464942-chr12:29467954..29469867,2	K562	blood:
7	chr12:29458406..29460957-chr12:29462899..29465425,2	K562	blood:
8	chr12:29461962..29462875-chr12:29672549..29673138,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERGIC2-2	chr12:29462704-29462836	ENSG00000257176.1
2	lnc-ERGIC2-2	chr12:29460783-29460977	NONHSAT027487
3	lnc-ERGIC2-2	chr12:29470641-29470781	ENSG00000257176.1
4	lnc-ERGIC2-2	chr12:29462704-29462836	NONHSAT027487
5	lnc-ERGIC2-2	chr12:29470641-29470781	NONHSAT027487
6	lnc-ERGIC2-2	chr12:29460783-29460977	ENSG00000257176.1
7	lnc-ERGIC2-2	chr12:29460783-29460977	ENSG00000245593
8	lnc-ERGIC2-2	chr12:29462704-29462836	ENSG00000245593

Variant related genes	Relation type
ENSG00000257176	TF binding region
FAR2	TF binding region
ENSG00000257176	CpG island
FAR2	CpG island
ENSG00000257456	chromatin interactions
LIN28B	miRNA target sites
TAF15	miRNA target sites

Extended variants
information (count: 423 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11609540	chr12:29458556-29458557	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs16934124	chr12:29458616-29458617	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150261729	chr12:29458627-29458628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575570487	chr12:29458629-29458630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546082186	chr12:29458662-29458663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375788298	chr12:29458672-29458673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183806687	chr12:29458679-29458680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188912354	chr12:29458681-29458682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561795925	chr12:29458755-29458756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147932217	chr12:29458760-29458761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559685891	chr12:29458772-29458773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75887502	chr12:29458781-29458782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550586988	chr12:29458814-29458815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568861841	chr12:29458854-29458855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193120312	chr12:29458905-29458906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78849682	chr12:29458930-29458931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75584328	chr12:29458931-29458932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551660668	chr12:29459134-29459135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115913546	chr12:29459145-29459146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12231997	chr12:29459168-29459169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533944991	chr12:29459243-29459244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185087551	chr12:29459269-29459270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574909511	chr12:29459283-29459284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7954278	chr12:29459290-29459291	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs557370018	chr12:29459293-29459294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575193525	chr12:29459297-29459298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187400397	chr12:29459369-29459370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191630416	chr12:29459379-29459380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570204850	chr12:29459383-29459384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564408465	chr12:29459514-29459515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117303218	chr12:29459607-29459608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141700235	chr12:29459728-29459729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7954871	chr12:29459732-29459733	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs536430326	chr12:29459736-29459737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61917164	chr12:29459812-29459813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146968920	chr12:29459822-29459823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552758511	chr12:29459899-29459900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562477343	chr12:29460000-29460001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532922277	chr12:29460008-29460009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138002309	chr12:29460078-29460079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184143321	chr12:29460115-29460116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527573702	chr12:29460129-29460130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549198910	chr12:29460266-29460267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12814180	chr12:29460278-29460279	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs370663697	chr12:29460287-29460288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149466641	chr12:29460300-29460301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535310710	chr12:29460319-29460320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376063306	chr12:29460340-29460341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71042984	chr12:29460341-29460342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138499564	chr12:29460348-29460349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	17133270	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29417200-29465400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr12:29422000-29465000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr12:29426800-29472800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr12:29427200-29527400	Weak transcription	Small Intestine	intestine
5	chr12:29429000-29460200	Weak transcription	Primary T cells from cord blood	blood
6	chr12:29429200-29463600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr12:29429400-29460400	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr12:29435400-29467200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:29439600-29464000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:29439600-29469400	Weak transcription	NH-A	brain
11	chr12:29443400-29460200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr12:29446200-29465000	Weak transcription	Duodenum Mucosa	Duodenum
13	chr12:29449600-29470800	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr12:29452800-29465200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr12:29452800-29494200	Weak transcription	Lung	lung
16	chr12:29453000-29465200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:29453000-29472800	Weak transcription	Fetal Intestine Large	intestine
18	chr12:29453200-29461800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:29453800-29480000	Weak transcription	Gastric	stomach
20	chr12:29454400-29463800	Weak transcription	HUVEC	blood vessel
21	chr12:29454600-29475800	Weak transcription	Spleen	Spleen
22	chr12:29455200-29489400	Weak transcription	Primary B cells from cord blood	blood
23	chr12:29456000-29469600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:29456600-29465800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:29456600-29471000	Weak transcription	Fetal Intestine Small	intestine
26	chr12:29457000-29465200	Weak transcription	Adipose Nuclei	Adipose
27	chr12:29457000-29467400	Weak transcription	Left Ventricle	heart
28	chr12:29457600-29470600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr12:29458000-29460000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:29458400-29459800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr12:29458600-29467400	Weak transcription	Brain Anterior Caudate	brain
32	chr12:29459200-29460800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr12:29459200-29462600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr12:29459200-29464800	Weak transcription	Dnd41	blood
35	chr12:29459400-29471400	Weak transcription	Liver	Liver
36	chr12:29459400-29493000	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr12:29459600-29472800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr12:29459600-29476000	Weak transcription	Fetal Thymus	thymus
39	chr12:29459800-29461200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr12:29459800-29465000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:29460000-29461800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:29460200-29460600	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr12:29460200-29461400	Strong transcription	Primary T cells from cord blood	blood
44	chr12:29460200-29476000	Weak transcription	Fetal Stomach	stomach
45	chr12:29460400-29467200	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr12:29460600-29461600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr12:29460600-29463800	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr12:29460800-29461200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr12:29460800-29470000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr12:29461200-29463600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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