Variant report

Variant	esv1848410
Chromosome Location	chr12:9621946-9751543
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 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	ARID3A	chr12:9743025-9743373	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:9740655-9741170	K562	blood:	n/a	n/a
3	ARID3A	chr12:9741257-9741854	HepG2	liver:	n/a	n/a
4	ATF1	chr12:9740572-9740926	K562	blood:	n/a	n/a
5	BACH1	chr12:9740595-9741065	K562	blood:	n/a	n/a
6	BACH1	chr12:9740652-9740897	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr12:9623145-9623344	GM12878	blood:	n/a	n/a
8	BATF	chr12:9627071-9627414	GM12878	blood:	n/a	chr12:9627229-9627240
9	BATF	chr12:9627069-9627370	GM12878	blood:	n/a	chr12:9627229-9627240
10	CCNT2	chr12:9740427-9741071	K562	blood:	n/a	n/a
11	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
12	CEBPB	chr12:9626864-9627128	K562	blood:	n/a	chr12:9626967-9626978
13	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
14	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
15	CEBPB	chr12:9626831-9627127	Hela-S3	cervix:	n/a	chr12:9626967-9626978
16	CEBPB	chr12:9626847-9627088	A549	lung:	n/a	chr12:9626967-9626978
17	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:9728216-9728457	A549	lung:	n/a	n/a
19	CEBPB	chr12:9626823-9627139	HepG2	liver:	n/a	chr12:9626967-9626978
20	CEBPB	chr12:9741394-9741705	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:9626941-9627031	K562	blood:	n/a	chr12:9626967-9626978
22	CEBPZ	chr12:9741497-9741533	HepG2	liver:	n/a	n/a
23	CTCF	chr12:9665377-9665602	K562	blood:	n/a	n/a
24	CTCF	chr12:9665360-9665590	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:9723300-9723450	HA-sp	spinal cord:	n/a	n/a
26	CTCF	chr12:9634643-9634716	GM19239	blood:	n/a	n/a
27	CTCF	chr12:9665315-9665625	A549	lung:	n/a	n/a
28	CTCF	chr12:9632078-9632163	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr12:9621433-9621970	SK-N-SH	brain:	n/a	chr12:9621901-9621914
30	CTCF	chr12:9665435-9665535	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:9621627-9621948	Spleen_OC	spleen:	n/a	chr12:9621901-9621914
32	CTCF	chr12:9726760-9726829	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr12:9709315-9709383	LNCaP	prostate:	n/a	n/a
34	CTCF	chr12:9665376-9665490	HepG2	liver:	n/a	n/a
35	CTCF	chr12:9665458-9665601	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr12:9730978-9731104	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr12:9695857-9695928	GM13976	blood:	n/a	n/a
38	CTCF	chr12:9665432-9665541	GM19239	blood:	n/a	n/a
39	CTCF	chr12:9632112-9632186	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:9621604-9621956	A549	lung:	n/a	chr12:9621901-9621914
41	CTCF	chr12:9621624-9621967	IMR90	lung:	n/a	chr12:9621901-9621914
42	CTCF	chr12:9631691-9631725	GM20000	blood:	n/a	n/a
43	CTCF	chr12:9665305-9665671	A549	lung:	n/a	n/a
44	CTCF	chr12:9665370-9665597	HepG2	liver:	n/a	n/a
45	CTCF	chr12:9669822-9669862	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr12:9691655-9691786	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:9665360-9665558	A549	lung:	n/a	n/a
48	CTCF	chr12:9634646-9634695	GM12891	blood:	n/a	n/a
49	CTCF	chr12:9634822-9634891	GM12891	blood:	n/a	n/a
50	CTCF	chr12:9665374-9665581	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9723402-9723452	GM06990	blood:	n/a
2	chr12:9722091-9722141	Jurkat	blood:	n/a
3	chr12:9720090-9720140	HRE	kidney:	n/a
4	chr12:9720554-9720604	AG09309	skin:	n/a
5	chr12:9723402-9723452	SK-N-MC	brain:	n/a
6	chr12:9722091-9722141	SAEC	small airway:	n/a
7	chr12:9722091-9722141	HepG2	liver:	n/a
8	chr12:9720090-9720140	NB4	blood:	n/a
9	chr12:9720090-9720140	PANC-1	pancreas:	n/a
10	chr12:9720554-9720604	HNPCEpiC	eye:	n/a
11	chr12:9723402-9723452	LNCaP	prostate:	n/a
12	chr12:9723402-9723452	NHBE	bronchial:	n/a
13	chr12:9720090-9720140	AoSMC	blood vessel:	n/a
14	chr12:9723402-9723452	AG04449	skin:	fetal
15	chr12:9720090-9720140	MCF-7	breast:	n/a
16	chr12:9722091-9722141	AG04450	lung:	fetal
17	chr12:9722091-9722141	HAEpiC	amniotic membrane:	n/a
18	chr12:9723402-9723452	HUVEC	blood vessel:	n/a
19	chr12:9720090-9720140	NHBE	bronchial:	n/a
20	chr12:9722091-9722141	NHBE	bronchial:	n/a
21	chr12:9720090-9720140	AG04449	skin:	fetal
22	chr12:9722091-9722141	GM19239	blood:	n/a
23	chr12:9720090-9720140	AG10803	skin:	n/a
24	chr12:9722091-9722141	SK-N-SH	brain:	n/a
25	chr12:9720554-9720604	AG10803	skin:	n/a
26	chr12:9720554-9720604	Caco-2	colon:	n/a
27	chr12:9720554-9720604	A549	lung:	n/a
28	chr12:9723402-9723452	HAEpiC	amniotic membrane:	n/a
29	chr12:9723402-9723452	HNPCEpiC	eye:	n/a
30	chr12:9723402-9723452	HEK293	kidney:	embryo
31	chr12:9722091-9722141	Hepatocyte	liver:	n/a
32	chr12:9720090-9720140	AG09309	skin:	n/a
33	chr12:9720554-9720604	HPAEpiC	pulmonary alveolar:	n/a
34	chr12:9720554-9720604	HRCEpiC	kidney:	n/a
35	chr12:9720554-9720604	GM12892	blood:	n/a
36	chr12:9723402-9723452	K562	blood:	n/a
37	chr12:9722091-9722141	BE2_C	brain:	n/a
38	chr12:9720554-9720604	IMR90	lung:	fetal
39	chr12:9720554-9720604	NT2-D1	testis:	n/a
40	chr12:9723402-9723452	AG09319	gingival:	n/a
41	chr12:9720554-9720604	NH-A	brain:	n/a
42	chr12:9720554-9720604	LNCaP	prostate:	n/a
43	chr12:9720090-9720140	T-47D	breast:	n/a
44	chr12:9720090-9720140	K562	blood:	n/a
45	chr12:9722091-9722141	H1-hESC	embryonic stem cell:	embryo
46	chr12:9720090-9720140	NT2-D1	testis:	n/a
47	chr12:9720554-9720604	GM19239	blood:	n/a
48	chr12:9720090-9720140	A549	lung:	n/a
49	chr12:9723402-9723452	AG09309	skin:	n/a
50	chr12:9723402-9723452	PrEC	prostate:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9740551..9742492-chr12:9759137..9760711,2	K562	blood:
2	chr12:9739995..9741756-chr12:9800822..9803051,2	K562	blood:
3	chr12:9530894..9532008-chr12:9621312..9622244,4	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-9	chr12:9725984-9726130	NONHSAT026830
2	lnc-CLEC2D-9	chr12:9724057-9724169	NONHSAT026830
3	lnc-CLEC2D-9	chr12:9725599-9725666	NONHSAT026830
4	lnc-CLEC2D-9	chr12:9727443-9727545	NONHSAT026830
5	lnc-KLRB1-2	chr12:9691704-9691933	l_603_chr12:9690762-9691933_testes
6	lnc-CLEC2D-9	chr12:9728239-9728313	NONHSAT026830
7	lnc-KLRB1-2	chr12:9690763-9691239	l_603_chr12:9690762-9691933_testes
8	lnc-CLEC2D-9	chr12:9728714-9728863	NONHSAT026830
9	lnc-CLEC2D-9	chr12:9723357-9723488	NONHSAT026830

No data

Variant related genes	Relation type
ENSG00000266633	TF binding region
ENSG00000256975	TF binding region
ENSG00000214776	TF binding region
ENSG00000266633	CpG island
ENSG00000256975	CpG island
ENSG00000214776	CpG island
ENSG00000111796	chromatin interactions

Extended variants
information (count: 2733 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2733 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375121844	chr12:9622061-9622062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2536679	chr12:9622208-9622209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2536678	chr12:9622210-9622211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11051147	chr12:9622323-9622324	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs2536677	chr12:9622351-9622352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550585118	chr12:9622368-9622369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141541796	chr12:9622496-9622497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374703050	chr12:9622499-9622500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs55858278	chr12:9622500-9622501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377339703	chr12:9622515-9622516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201882355	chr12:9622516-9622517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191566926	chr12:9622524-9622525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113721196	chr12:9622527-9622528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182271526	chr12:9622645-9622646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7299330	chr12:9622671-9622672	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs145997164	chr12:9622685-9622686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs61913568	chr12:9622692-9622693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201208185	chr12:9622802-9622803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4764120	chr12:9622803-9622804	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs112316362	chr12:9622822-9622823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191453291	chr12:9622846-9622847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140097185	chr12:9622855-9622856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74899303	chr12:9622863-9622864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558761157	chr12:9622999-9623000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139260538	chr12:9623078-9623079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115285646	chr12:9623145-9623146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184764744	chr12:9623165-9623166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11608635	chr12:9623175-9623176	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11447512	chr12:9623207-9623208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11440580	chr12:9623208-9623209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs397940169	chr12:9623212-9623213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149972302	chr12:9623299-9623300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149217196	chr12:9623334-9623335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555018919	chr12:9623375-9623376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189134299	chr12:9623413-9623414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192856233	chr12:9623495-9623496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114591908	chr12:9623578-9623579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10743737	chr12:9623616-9623617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs150296700	chr12:9623684-9623685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7138356	chr12:9623783-9623784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112881185	chr12:9623803-9623804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185417455	chr12:9623816-9623817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10743738	chr12:9623841-9623842	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs2536676	chr12:9623963-9623964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2536675	chr12:9623964-9623965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189527202	chr12:9623974-9623975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142649610	chr12:9623992-9623993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562727396	chr12:9624005-9624006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs55655311	chr12:9624045-9624046	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs369240827	chr12:9624095-9624096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9607200-9623000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:9608800-9642800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:9615400-9622600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr12:9617800-9622800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr12:9618200-9622600	Weak transcription	GM12878-XiMat	blood
6	chr12:9619600-9623600	Enhancers	Fetal Thymus	thymus
7	chr12:9620800-9623600	Enhancers	Primary T cells from cord blood	blood
8	chr12:9620800-9623600	Enhancers	Primary T cells fromperipheralblood	blood
9	chr12:9621000-9622000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr12:9621000-9622000	Enhancers	HepG2	liver
11	chr12:9621000-9622200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr12:9621000-9623600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:9621400-9622000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr12:9621400-9622000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:9621400-9622400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr12:9621400-9623600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr12:9621600-9622000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr12:9621600-9622000	Enhancers	Liver	Liver
19	chr12:9621600-9622000	Enhancers	Fetal Lung	lung
20	chr12:9621600-9622000	Enhancers	Dnd41	blood
21	chr12:9621800-9622600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr12:9621800-9622800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr12:9621800-9623000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr12:9621800-9623000	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr12:9621800-9623000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr12:9621800-9623600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr12:9621800-9625800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:9622000-9622400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr12:9622000-9622400	Weak transcription	Dnd41	blood
30	chr12:9622000-9622800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr12:9622000-9623000	Weak transcription	Thymus	Thymus
32	chr12:9622000-9624000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr12:9622000-9625800	Weak transcription	Fetal Lung	lung
34	chr12:9622200-9622600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr12:9622400-9622800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr12:9622400-9623200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:9622400-9623600	Enhancers	Dnd41	blood
38	chr12:9622600-9623200	Enhancers	GM12878-XiMat	blood
39	chr12:9622600-9623400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr12:9622600-9623600	Enhancers	Primary B cells from peripheral blood	blood
41	chr12:9622600-9623600	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr12:9622800-9623200	Enhancers	Primary hematopoietic stem cells	blood
43	chr12:9622800-9623600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr12:9622800-9623600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr12:9622800-9623600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:9623000-9623400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:9623000-9623600	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr12:9623000-9623600	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr12:9623000-9623600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr12:9623000-9623600	Enhancers	Thymus	Thymus

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