Variant report

Variant	nsv819469
Chromosome Location	chr12:29285461-29303486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:316)
CpG islands
(count:854)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:29299199-29299376	K562	blood:	n/a	n/a
2	ATF2	chr12:29301888-29302308	GM12878	blood:	n/a	n/a
3	BACH1	chr12:29301402-29302837	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr12:29301015-29301680	K562	blood:	n/a	chr12:29301191-29301200 chr12:29301190-29301199 chr12:29301190-29301199
5	BHLHE40	chr12:29301107-29301264	A549	lung:	n/a	chr12:29301191-29301200 chr12:29301190-29301199 chr12:29301190-29301199
6	BHLHE40	chr12:29301082-29301377	GM12878	blood:	n/a	chr12:29301191-29301200 chr12:29301190-29301199 chr12:29301190-29301199
7	BHLHE40	chr12:29301956-29302429	K562	blood:	n/a	n/a
8	CCNT2	chr12:29301916-29302627	K562	blood:	n/a	chr12:29302353-29302362 chr12:29301930-29301939
9	CHD1	chr12:29301105-29301850	H1-hESC	embryonic stem cell:	n/a	chr12:29301793-29301800
10	CHD1	chr12:29302110-29302416	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr12:29301319-29302428	H1-hESC	embryonic stem cell:	n/a	chr12:29302083-29302093 chr12:29301793-29301800
12	CHD2	chr12:29303204-29303210	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr12:29298445-29298584	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr12:29301910-29302045	GM12878	blood:	n/a	n/a
15	CREB1	chr12:29302395-29303101	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTBP2	chr12:29301919-29303217	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr12:29301440-29301590	HAc	cerebellar:	n/a	n/a
18	CTCF	chr12:29302042-29302060	GM12891	blood:	n/a	n/a
19	CTCF	chr12:29301660-29301810	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr12:29301501-29301601	GM19239	blood:	n/a	n/a
21	CTCF	chr12:29301900-29302050	GM12864	blood:	n/a	n/a
22	CTCF	chr12:29301780-29301930	AG09319	gingival:	n/a	n/a
23	CTCF	chr12:29301781-29301785	Gliobla	brain:	n/a	n/a
24	CTCF	chr12:29301800-29301950	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr12:29301660-29301810	GM12873	blood:	n/a	n/a
26	CTCF	chr12:29301840-29301990	HAc	cerebellar:	n/a	n/a
27	CTCF	chr12:29303217-29303297	GM19239	blood:	n/a	n/a
28	CTCF	chr12:29301760-29301910	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr12:29301700-29301850	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr12:29302080-29302230	AG04449	skin:	n/a	n/a
31	CTCF	chr12:29301673-29301889	GM19238	blood:	n/a	n/a
32	CTCF	chr12:29301760-29301910	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr12:29301800-29301950	HMF	breast:	n/a	n/a
34	CTCF	chr12:29301620-29301770	GM12873	blood:	n/a	n/a
35	CTCF	chr12:29301760-29301910	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr12:29301660-29301810	BE2_C	brain:	n/a	n/a
37	CTCF	chr12:29301740-29301890	GM12866	blood:	n/a	n/a
38	CTCF	chr12:29301736-29301934	GM12878	blood:	n/a	n/a
39	CTCF	chr12:29301480-29301630	GM12874	blood:	n/a	n/a
40	CTCF	chr12:29301560-29301710	GM12864	blood:	n/a	n/a
41	CTCF	chr12:29303060-29303210	NB4	blood:	n/a	n/a
42	CTCF	chr12:29302038-29302041	GM12891	blood:	n/a	n/a
43	CTCF	chr12:29301640-29301790	AG04449	skin:	n/a	n/a
44	CTCF	chr12:29301680-29301830	GM06990	blood:	n/a	n/a
45	CTCF	chr12:29301740-29301890	GM12874	blood:	n/a	n/a
46	CTCF	chr12:29301730-29301783	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:29301920-29302070	GM12871	blood:	n/a	n/a
48	CTCF	chr12:29301700-29301850	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr12:29302200-29302350	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr12:29301787-29301834	GM12878	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:29301525-29301575	NB4	blood:	n/a
2	chr12:29302515-29302565	GM19239	blood:	n/a
3	chr12:29303160-29303210	HCPEpiC	choroid plexus:	n/a
4	chr12:29303219-29303269	SAEC	small airway:	n/a
5	chr12:29303219-29303269	HEEpiC	esophagus:	n/a
6	chr12:29302179-29302229	SKMC	muscle:	n/a
7	chr12:29303219-29303269	BJ	skin:	n/a
8	chr12:29301719-29301769	A549	lung:	n/a
9	chr12:29285982-29286032	HCT-116	colon:	n/a
10	chr12:29301525-29301575	AoSMC	blood vessel:	n/a
11	chr12:29302035-29302085	AG04449	skin:	fetal
12	chr12:29301719-29301769	HIPEpiC	eye:	n/a
13	chr12:29303184-29303234	HCM	heart:	n/a
14	chr12:29301719-29301769	NH-A	brain:	n/a
15	chr12:29301719-29301769	RPTEC	kidney:	n/a
16	chr12:29302279-29302329	HNPCEpiC	eye:	n/a
17	chr12:29301719-29301769	SK-N-SH_RA	brain:	n/a
18	chr12:29301525-29301575	NHDF-neo	bronchial:	n/a
19	chr12:29303160-29303210	NB4	blood:	n/a
20	chr12:29299659-29299709	AG04450	lung:	fetal
21	chr12:29301719-29301769	PrEC	prostate:	n/a
22	chr12:29302714-29302764	ovcar-3	ovarian:	n/a
23	chr12:29303219-29303269	AG04450	lung:	fetal
24	chr12:29302179-29302229	HIPEpiC	eye:	n/a
25	chr12:29303160-29303210	NT2-D1	testis:	n/a
26	chr12:29301719-29301769	AG09319	gingival:	n/a
27	chr12:29303160-29303210	SK-N-MC	brain:	n/a
28	chr12:29303184-29303234	GM19239	blood:	n/a
29	chr12:29299659-29299709	SK-N-MC	brain:	n/a
30	chr12:29301525-29301575	AG09319	gingival:	n/a
31	chr12:29302279-29302329	Jurkat	blood:	n/a
32	chr12:29303219-29303269	NHBE	bronchial:	n/a
33	chr12:29303160-29303210	PrEC	prostate:	n/a
34	chr12:29302714-29302764	HUVEC	blood vessel:	n/a
35	chr12:29302714-29302764	PFSK-1	brain:	n/a
36	chr12:29303184-29303234	BE2_C	brain:	n/a
37	chr12:29285982-29286032	GM12891	blood:	n/a
38	chr12:29303219-29303269	Hela-S3	cervix:	n/a
39	chr12:29285982-29286032	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:29299659-29299709	PANC-1	pancreas:	n/a
41	chr12:29301525-29301575	Hela-S3	cervix:	n/a
42	chr12:29302714-29302764	SKMC	muscle:	n/a
43	chr12:29301525-29301575	HNPCEpiC	eye:	n/a
44	chr12:29301525-29301575	NH-A	brain:	n/a
45	chr12:29302035-29302085	SK-N-MC	brain:	n/a
46	chr12:29302279-29302329	NHDF-neo	bronchial:	n/a
47	chr12:29302179-29302229	HCM	heart:	n/a
48	chr12:29302231-29302281	HAEpiC	amniotic membrane:	n/a
49	chr12:29303219-29303269	A549	lung:	n/a
50	chr12:29302231-29302281	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:29301993..29302516-chr6:31802207..31802861,2	NB4	blood:
2	chr12:29301948..29302516-chr6:28806299..28806949,2	NB4	blood:
3	chr12:29301993..29302856-chr5:180670405..180671354,2	NB4	blood:
4	chr12:29302116..29302733-chr13:52025571..52026304,2	NB4	blood:
5	chr11:88070898..88071694-chr12:29302232..29303122,2	NB4	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-677C1.2.1-3	chr12:29302253-29302340	NONHSAT027484
2	lnc-ERGIC2-4	chr12:29294264-29295242	XLOC_010037
3	lnc-ERGIC2-3	chr12:29301469-29301608	ENSG00000257258
4	lnc-ERGIC2-4	chr12:29301115-29301212	XLOC_010037
5	lnc-ERGIC2-3	chr12:29296129-29296581	ENSG00000257258
6	lnc-RP11-677C1.2.1-3	chr12:29302143-29302340	NONHSAT027482

No data

Variant related genes	Relation type
ENSG00000257258	TF binding region
FAR2	TF binding region
ENSG00000257258	CpG island
FAR2	CpG island
ENSG00000225173	chromatin interactions
ENSG00000204387	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000204628	chromatin interactions
ENSG00000109861	chromatin interactions

Extended variants
information (count: 340 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144035789	chr12:29285465-29285466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534154137	chr12:29285469-29285470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190769956	chr12:29285492-29285493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2060566	chr12:29285531-29285532	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs538531449	chr12:29285569-29285570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11050071	chr12:29285577-29285578	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs141577380	chr12:29285582-29285583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181643009	chr12:29285588-29285589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538990309	chr12:29285607-29285608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185750553	chr12:29285628-29285629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117059651	chr12:29285658-29285659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs118030809	chr12:29285674-29285675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543155294	chr12:29285709-29285710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112372960	chr12:29285730-29285731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs531553547	chr12:29285773-29285774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12309591	chr12:29285777-29285778	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs202035230	chr12:29285784-29285785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543675973	chr12:29285792-29285793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201834050	chr12:29285798-29285799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369165099	chr12:29285800-29285801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369153515	chr12:29285817-29285818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188992524	chr12:29285847-29285848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551925361	chr12:29285851-29285852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111233856	chr12:29285919-29285920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs559761904	chr12:29285939-29285940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181049410	chr12:29285942-29285943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546129906	chr12:29285943-29285944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538192947	chr12:29285945-29285946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185473241	chr12:29285982-29285983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7969790	chr12:29285987-29285988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538816007	chr12:29285997-29285998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144062919	chr12:29286021-29286022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148672392	chr12:29286028-29286029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142159433	chr12:29286071-29286072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77404172	chr12:29286115-29286116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147704159	chr12:29286117-29286118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140813793	chr12:29286130-29286131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183022065	chr12:29286195-29286196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144622243	chr12:29286202-29286203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75646116	chr12:29286237-29286238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371550016	chr12:29286238-29286239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559585520	chr12:29286245-29286246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527829918	chr12:29286249-29286250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549443973	chr12:29286276-29286277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs59190473	chr12:29286279-29286280	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs370122265	chr12:29286296-29286297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35105496	chr12:29286354-29286355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147866313	chr12:29286368-29286369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35918314	chr12:29286377-29286378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550224668	chr12:29286386-29286387	Weak transcription Enhancers	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
Breast cancer	21364760	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29266400-29286400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:29284000-29285800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr12:29284600-29286000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr12:29284800-29286000	Weak transcription	NHEK	skin
5	chr12:29285200-29285600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr12:29285200-29286400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:29285400-29285800	Enhancers	Osteobl	bone
8	chr12:29285600-29285800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr12:29285800-29286400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr12:29285800-29286800	Weak transcription	Osteobl	bone
11	chr12:29286000-29286400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr12:29286000-29286800	Enhancers	NHEK	skin
13	chr12:29286000-29287200	Enhancers	HMEC	breast
14	chr12:29286400-29286800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr12:29286400-29287000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:29286400-29287200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr12:29286800-29287200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:29286800-29287200	Enhancers	Osteobl	bone
19	chr12:29298200-29299400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr12:29298400-29298600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr12:29298400-29298600	Enhancers	Fetal Muscle Trunk	muscle
22	chr12:29298400-29298800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:29298400-29299000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr12:29298400-29299600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr12:29298400-29299600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr12:29298600-29299400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr12:29298600-29300600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:29298600-29301000	Weak transcription	Fetal Muscle Trunk	muscle
29	chr12:29298800-29299600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:29298800-29300000	Enhancers	Primary hematopoietic stem cells	blood
31	chr12:29299000-29299200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr12:29299000-29299600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:29299000-29300600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:29299000-29301200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr12:29299200-29299800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr12:29299200-29300800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr12:29299400-29300400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr12:29299400-29300600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr12:29299600-29300200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:29299600-29300600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr12:29299600-29301000	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr12:29299600-29301200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:29299800-29300200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr12:29300000-29300400	Weak transcription	Primary hematopoietic stem cells	blood
45	chr12:29300200-29300600	Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr12:29300200-29301000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:29300200-29301600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:29300400-29300600	Enhancers	Primary hematopoietic stem cells	blood
49	chr12:29300400-29300600	Enhancers	NHDF-Ad	bronchial
50	chr12:29300400-29301000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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