Variant report

Variant	nsv976566
Chromosome Location	chr12:9469779-9481646
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	BHLHE40	chr12:9472155-9472656	GM12878	blood:	n/a	n/a
2	BHLHE40	chr12:9472400-9472633	K562	blood:	n/a	n/a
3	BRCA1	chr12:9480340-9480381	GM12878	blood:	n/a	n/a
4	CTCF	chr12:9471900-9472050	GM12870	blood:	n/a	chr12:9472004-9472017
5	CTCF	chr12:9471936-9472127	GM10266	blood:	n/a	chr12:9472004-9472017
6	CTCF	chr12:9471937-9472065	Pancreas_OC	pancreas:	n/a	chr12:9472004-9472017
7	CTCF	chr12:9471920-9472070	HA-sp	spinal cord:	n/a	chr12:9472004-9472017
8	CTCF	chr12:9471912-9472099	K562	blood:	n/a	chr12:9472004-9472017
9	CTCF	chr12:9477440-9477590	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr12:9471894-9472090	A549	lung:	n/a	chr12:9472004-9472017
11	CTCF	chr12:9472000-9472150	Hela-S3	cervix:	n/a	chr12:9472004-9472017
12	CTCF	chr12:9471900-9472050	Hela-S3	cervix:	n/a	chr12:9472004-9472017
13	CTCF	chr12:9471920-9472070	GM12864	blood:	n/a	chr12:9472004-9472017
14	CTCF	chr12:9471971-9472126	LNCaP	prostate:	n/a	chr12:9472004-9472017
15	CTCF	chr12:9471920-9472070	HPF	lung:	n/a	chr12:9472004-9472017
16	CTCF	chr12:9471918-9472128	GM19240	blood:	n/a	chr12:9472004-9472017
17	CTCF	chr12:9471920-9472070	K562	blood:	n/a	chr12:9472004-9472017
18	CTCF	chr12:9471969-9472101	A549	lung:	n/a	chr12:9472004-9472017
19	CTCF	chr12:9471840-9471990	GM06990	blood:	n/a	n/a
20	CTCF	chr12:9471922-9472110	GM12878	blood:	n/a	chr12:9472004-9472017
21	CTCF	chr12:9471900-9472050	GM12875	blood:	n/a	chr12:9472004-9472017
22	CTCF	chr12:9471920-9472070	HFF-Myc	foreskin:	n/a	chr12:9472004-9472017
23	CTCF	chr12:9471900-9472050	GM12864	blood:	n/a	chr12:9472004-9472017
24	CTCF	chr12:9471920-9472070	WERI-Rb-1	eye:	n/a	chr12:9472004-9472017
25	CTCF	chr12:9471916-9472119	MCF-7	breast:	n/a	chr12:9472004-9472017
26	CTCF	chr12:9471794-9472308	SK-N-SH	brain:	n/a	chr12:9472004-9472017
27	CTCF	chr12:9471908-9472108	GM19239	blood:	n/a	chr12:9472004-9472017
28	CTCF	chr12:9471936-9472080	Hela-S3	cervix:	n/a	chr12:9472004-9472017
29	CTCF	chr12:9471972-9472088	Spleen_OC	spleen:	n/a	chr12:9472004-9472017
30	CTCF	chr12:9471921-9472108	GM12891	blood:	n/a	chr12:9472004-9472017
31	CTCF	chr12:9471880-9472030	HCT-116	colon:	n/a	chr12:9472004-9472017
32	CTCF	chr12:9471900-9472050	HBMEC	blood vessel:	n/a	chr12:9472004-9472017
33	CTCF	chr12:9475237-9475264	GM10266	blood:	n/a	n/a
34	CTCF	chr12:9471920-9472070	BJ	skin:	n/a	chr12:9472004-9472017
35	CTCF	chr12:9471900-9472050	HCFaa	heart:	n/a	chr12:9472004-9472017
36	CTCF	chr12:9471880-9472030	NHLF	lung:	n/a	chr12:9472004-9472017
37	CTCF	chr12:9471920-9472070	HepG2	liver:	n/a	chr12:9472004-9472017
38	CTCF	chr12:9471840-9471990	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr12:9471976-9472064	GM10248	blood:	n/a	chr12:9472004-9472017
40	CTCF	chr12:9471952-9472078	H1-hESC	embryonic stem cell:	n/a	chr12:9472004-9472017
41	CTCF	chr12:9477548-9477606	GM13977	blood:	n/a	n/a
42	CTCF	chr12:9471940-9472090	GM12865	blood:	n/a	chr12:9472004-9472017
43	CTCF	chr12:9471908-9472119	MCF-7	breast:	n/a	chr12:9472004-9472017
44	CTCF	chr12:9471920-9472070	HRPEpiC	eye:	n/a	chr12:9472004-9472017
45	CTCF	chr12:9471920-9472070	AG09309	skin:	n/a	chr12:9472004-9472017
46	CTCF	chr12:9471897-9472134	MCF-7	breast:	n/a	chr12:9472004-9472017
47	CTCF	chr12:9471941-9472050	SK-N-SH_RA	brain:	n/a	chr12:9472004-9472017
48	CTCF	chr12:9471940-9472090	GM12872	blood:	n/a	chr12:9472004-9472017
49	CTCF	chr12:9471940-9472118	GM13977	blood:	n/a	chr12:9472004-9472017
50	CTCF	chr12:9471920-9472070	GM12801	blood:	n/a	chr12:9472004-9472017

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9478627-9478677	ovcar-3	ovarian:	n/a
2	chr12:9478612-9478662	HepG2	liver:	n/a
3	chr12:9478906-9478956	IMR90	lung:	fetal
4	chr12:9478627-9478677	GM19239	blood:	n/a
5	chr12:9478612-9478662	PrEC	prostate:	n/a
6	chr12:9479566-9479616	NHBE	bronchial:	n/a
7	chr12:9478627-9478677	NH-A	brain:	n/a
8	chr12:9478627-9478677	A549	lung:	n/a
9	chr12:9478906-9478956	NB4	blood:	n/a
10	chr12:9478906-9478956	GM19239	blood:	n/a
11	chr12:9479566-9479616	PANC-1	pancreas:	n/a
12	chr12:9479566-9479616	HL-60	blood:	n/a
13	chr12:9478612-9478662	H1-hESC	embryonic stem cell:	embryo
14	chr12:9478612-9478662	HEK293	kidney:	embryo
15	chr12:9478627-9478677	HL-60	blood:	n/a
16	chr12:9478906-9478956	HCT-116	colon:	n/a
17	chr12:9478906-9478956	NT2-D1	testis:	n/a
18	chr12:9478612-9478662	LNCaP	prostate:	n/a
19	chr12:9478612-9478662	PANC-1	pancreas:	n/a
20	chr12:9479566-9479616	BE2_C	brain:	n/a
21	chr12:9479566-9479616	GM12878	blood:	n/a
22	chr12:9478627-9478677	HAEpiC	amniotic membrane:	n/a
23	chr12:9478612-9478662	AG04450	lung:	fetal
24	chr12:9478906-9478956	Hela-S3	cervix:	n/a
25	chr12:9478612-9478662	T-47D	breast:	n/a
26	chr12:9478906-9478956	HRPEpiC	eye:	n/a
27	chr12:9479566-9479616	BJ	skin:	n/a
28	chr12:9479566-9479616	HRCEpiC	kidney:	n/a
29	chr12:9478612-9478662	SAEC	small airway:	n/a
30	chr12:9479566-9479616	CMK	blood:	n/a
31	chr12:9479566-9479616	AG04450	lung:	fetal
32	chr12:9479566-9479616	MCF10A-Er-Src	breast:	n/a
33	chr12:9479566-9479616	HEK293	kidney:	embryo
34	chr12:9478906-9478956	HCPEpiC	choroid plexus:	n/a
35	chr12:9478906-9478956	SK-N-SH	brain:	n/a
36	chr12:9479566-9479616	LNCaP	prostate:	n/a
37	chr12:9478906-9478956	U87	brain:	n/a
38	chr12:9478612-9478662	SK-N-SH_RA	brain:	n/a
39	chr12:9478906-9478956	PrEC	prostate:	n/a
40	chr12:9478612-9478662	MCF-7	breast:	n/a
41	chr12:9478627-9478677	AG09319	gingival:	n/a
42	chr12:9478627-9478677	ProgFib	skin:	n/a
43	chr12:9478906-9478956	HRCEpiC	kidney:	n/a
44	chr12:9478627-9478677	MCF10A-Er-Src	breast:	n/a
45	chr12:9479566-9479616	IMR90	lung:	fetal
46	chr12:9478906-9478956	BJ	skin:	n/a
47	chr12:9478906-9478956	HRE	kidney:	n/a
48	chr12:9479566-9479616	AG10803	skin:	n/a
49	chr12:9478906-9478956	AoSMC	blood vessel:	n/a
50	chr12:9478906-9478956	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:9225166..9226787-chr12:9475945..9478723,2	MCF-7	breast:
2	chr12:9216487..9217272-chr12:9471486..9472478,2	MCF-7	breast:
3	chr12:9216104..9218306-chr12:9470179..9473467,3	MCF-7	breast:
4	chr12:9471764..9473665-chr12:9564371..9566160,2	MCF-7	breast:
5	chr12:9471846..9472542-chr12:9564639..9565202,2	MCF-7	breast:
6	chr12:9475880..9477662-chr12:9479960..9482900,2	K562	blood:
7	chr12:9215714..9219195-chr12:9470456..9473261,3	MCF-7	breast:
8	chr12:9475880..9477662-chr12:9479960..9482900,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRG1-7	chr12:9469938-9470103	NONHSAT026402
2	lnc-KLRG1-7	chr12:9470564-9470619	NONHSAT026402

Variant related genes	Relation type
ENSG00000255753	TF binding region
ENSG00000255753	CpG island
ENSG00000214851	chromatin interactions
ENSG00000245105	chromatin interactions

Extended variants
information (count: 429 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:429 , 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	rs190019893	chr12:9469787-9469788	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs367766571	chr12:9469811-9469812	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs56236944	chr12:9469846-9469847	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs61918193	chr12:9469854-9469855	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs181304920	chr12:9469888-9469889	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs185038671	chr12:9469909-9469910	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs373517578	chr12:9469954-9469955	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs75685042	chr12:9469965-9469966	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs139501491	chr12:9469984-9469985	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs189891606	chr12:9470000-9470001	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs200023765	chr12:9470011-9470012	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs377462333	chr12:9470016-9470017	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs182577680	chr12:9470022-9470023	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs188882696	chr12:9470023-9470024	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs7969222	chr12:9470120-9470121	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs192024638	chr12:9470126-9470127	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs183566468	chr12:9470168-9470169	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139090749	chr12:9470213-9470214	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs187616899	chr12:9470238-9470239	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs112323048	chr12:9470259-9470260	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs7956682	chr12:9470281-9470282	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs377583916	chr12:9470350-9470351	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs201024372	chr12:9470358-9470359	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs191731917	chr12:9470389-9470390	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188064931	chr12:9470410-9470411	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs540737450	chr12:9470445-9470446	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs184321038	chr12:9470447-9470448	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs368137273	chr12:9470603-9470604	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs564120085	chr12:9470654-9470655	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs367644589	chr12:9470657-9470658	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs577668477	chr12:9470671-9470672	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150425848	chr12:9470724-9470725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs7957287	chr12:9470769-9470770	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs10843400	chr12:9470831-9470832	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs372029492	chr12:9470847-9470848	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs549141354	chr12:9470848-9470849	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs10771522	chr12:9470893-9470894	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs186787714	chr12:9470993-9470994	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs139314582	chr12:9471014-9471015	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs10743659	chr12:9471036-9471037	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs143779694	chr12:9471071-9471072	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs191242634	chr12:9471106-9471107	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs184386900	chr12:9471107-9471108	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs190522673	chr12:9471112-9471113	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs148136244	chr12:9471152-9471153	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs57742668	chr12:9471158-9471159	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs376654249	chr12:9471181-9471182	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs10843404	chr12:9471215-9471216	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs199538885	chr12:9471246-9471247	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs56403355	chr12:9471286-9471287	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance

Variant related diseases (count:80)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	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
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9437200-9472400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr12:9437200-9485200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:9437400-9470800	Weak transcription	Brain Germinal Matrix	brain
4	chr12:9450200-9471400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr12:9456200-9472200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr12:9456400-9471800	Weak transcription	GM12878-XiMat	blood
7	chr12:9457400-9485800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr12:9458000-9472200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:9463000-9479000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:9463200-9471600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr12:9464400-9477600	Weak transcription	Lung	lung
12	chr12:9464600-9487600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr12:9464800-9472200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr12:9464800-9472200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr12:9464800-9490000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr12:9465000-9472600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr12:9465000-9473000	Weak transcription	Esophagus	oesophagus
18	chr12:9465000-9486400	Weak transcription	A549	lung
19	chr12:9465200-9471400	Weak transcription	Spleen	Spleen
20	chr12:9465400-9485200	Weak transcription	Fetal Intestine Small	intestine
21	chr12:9465600-9471000	Weak transcription	Fetal Stomach	stomach
22	chr12:9465600-9472200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:9465600-9477800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:9465600-9484000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr12:9465600-9488000	Weak transcription	Dnd41	blood
26	chr12:9466000-9484000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr12:9466200-9472400	Weak transcription	HMEC	breast
28	chr12:9466200-9484000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:9466400-9470200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr12:9466400-9471600	Weak transcription	Fetal Muscle Leg	muscle
31	chr12:9466400-9471600	Weak transcription	Fetal Thymus	thymus
32	chr12:9466400-9471800	Weak transcription	Thymus	Thymus
33	chr12:9466400-9472000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:9466400-9477400	Weak transcription	Fetal Lung	lung
35	chr12:9466400-9485200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr12:9466400-9487200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr12:9466400-9487600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:9466600-9470000	Weak transcription	HepG2	liver
39	chr12:9468800-9471000	Weak transcription	Fetal Muscle Trunk	muscle
40	chr12:9470000-9472800	Enhancers	HepG2	liver
41	chr12:9470800-9471200	Enhancers	Primary T cells from cord blood	blood
42	chr12:9470800-9472400	Enhancers	Brain Germinal Matrix	brain
43	chr12:9471000-9471200	Enhancers	Fetal Muscle Trunk	muscle
44	chr12:9471200-9471600	Weak transcription	Primary T cells from cord blood	blood
45	chr12:9471600-9471800	Enhancers	Primary T cells from cord blood	blood
46	chr12:9471600-9471800	Enhancers	Spleen	Spleen
47	chr12:9471600-9472000	Enhancers	Fetal Muscle Leg	muscle
48	chr12:9471600-9472200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr12:9471600-9473000	Enhancers	Fetal Thymus	thymus
50	chr12:9471600-9473400	Enhancers	Primary B cells from peripheral blood	blood

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