Variant report

Variant	nsv973014
Chromosome Location	chr12:8166756-8171787
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:117)
CpG islands
(count:306)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:117 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:8169533-8169537	K562	blood:	n/a	n/a
2	BHLHE40	chr12:8171613-8171614	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:8171471-8171635	K562	blood:	n/a	n/a
4	CHD2	chr12:8171454-8172171	H1-hESC	embryonic stem cell:	n/a	n/a
5	CREB1	chr12:8171260-8171899	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTBP2	chr12:8171243-8172072	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr12:8171580-8171730	AG09319	gingival:	n/a	n/a
8	CTCF	chr12:8171520-8171670	AG04449	skin:	n/a	n/a
9	CTCF	chr12:8171500-8171650	GM12867	blood:	n/a	n/a
10	CTCF	chr12:8171560-8171710	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr12:8171560-8171710	HRE	kidney:	n/a	n/a
12	CTCF	chr12:8171640-8171790	GM12871	blood:	n/a	n/a
13	CTCF	chr12:8171590-8171648	K562	blood:	n/a	n/a
14	CTCF	chr12:8171560-8171710	GM12871	blood:	n/a	n/a
15	CTCF	chr12:8171520-8171670	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr12:8171540-8171690	K562	blood:	n/a	n/a
17	CTCF	chr12:8171500-8171650	NB4	blood:	n/a	n/a
18	CTCF	chr12:8171658-8171681	K562	blood:	n/a	n/a
19	CTCF	chr12:8171600-8171750	GM12874	blood:	n/a	n/a
20	CTCF	chr12:8171460-8171610	HAc	cerebellar:	n/a	n/a
21	CTCF	chr12:8171545-8171697	HepG2	liver:	n/a	n/a
22	CTCF	chr12:8171600-8171750	GM12870	blood:	n/a	n/a
23	CTCF	chr12:8171560-8171710	HCT-116	colon:	n/a	n/a
24	CTCF	chr12:8171547-8171668	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr12:8171480-8171630	AG04450	lung:	n/a	n/a
26	CTCF	chr12:8171720-8171870	GM12872	blood:	n/a	n/a
27	CTCF	chr12:8171420-8171570	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr12:8171540-8171690	BJ	skin:	n/a	n/a
29	CTCF	chr12:8171560-8171710	HepG2	liver:	n/a	n/a
30	CTCF	chr12:8171540-8171690	WERI-Rb-1	eye:	n/a	n/a
31	E2F6	chr12:8171170-8171953	H1-hESC	embryonic stem cell:	n/a	chr12:8171358-8171368 chr12:8171363-8171372
32	E2F6	chr12:8171257-8171824	K562	blood:	n/a	chr12:8171358-8171368 chr12:8171363-8171372
33	E2F6	chr12:8171087-8172099	H1-hESC	embryonic stem cell:	n/a	chr12:8171358-8171368 chr12:8171363-8171372
34	ELF1	chr12:8167482-8167745	K562	blood:	n/a	n/a
35	EP300	chr12:8171432-8171951	H1-hESC	embryonic stem cell:	n/a	chr12:8171745-8171761 chr12:8171684-8171693
36	GATA1	chr12:8171154-8171838	PBDE	blood:	n/a	n/a
37	GATA2	chr12:8171204-8171532	SH-SY5Y	brain:	n/a	n/a
38	GTF2F1	chr12:8171530-8171753	H1-hESC	embryonic stem cell:	n/a	n/a
39	HCFC1	chr12:8167644-8167668	K562	blood:	n/a	n/a
40	HCFC1	chr12:8171441-8171628	K562	blood:	n/a	n/a
41	HDAC2	chr12:8171415-8171652	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUND	chr12:8171522-8171569	K562	blood:	n/a	n/a
43	JUND	chr12:8171523-8172076	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr12:8171181-8172230	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr12:8167535-8167738	K562	blood:	n/a	n/a
46	MAX	chr12:8171254-8172207	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAX	chr12:8171229-8171863	K562	blood:	n/a	n/a
48	MAX	chr12:8171638-8171793	K562	blood:	n/a	n/a
49	MAX	chr12:8171275-8171912	NB4	blood:	n/a	n/a
50	MAX	chr12:8171242-8171955	H1-hESC	embryonic stem cell:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8171633-8171683	ProgFib	skin:	n/a
2	chr12:8171633-8171683	ProgFib	skin:	n/a
3	chr12:8167594-8167644	SK-N-SH_RA	brain:	n/a
4	chr12:8171463-8171513	HNPCEpiC	eye:	n/a
5	chr12:8171686-8171736	GM12891	blood:	n/a
6	chr12:8171463-8171513	NHBE	bronchial:	n/a
7	chr12:8171463-8171513	AG10803	skin:	n/a
8	chr12:8171686-8171736	Hela-S3	cervix:	n/a
9	chr12:8170797-8170847	HepG2	liver:	n/a
10	chr12:8167594-8167644	Caco-2	colon:	n/a
11	chr12:8167594-8167644	HCF	heart:	n/a
12	chr12:8170797-8170847	SAEC	small airway:	n/a
13	chr12:8167594-8167644	SK-N-SH	brain:	n/a
14	chr12:8171686-8171736	SAEC	small airway:	n/a
15	chr12:8171633-8171683	IMR90	lung:	fetal
16	chr12:8171633-8171683	HMEC	breast:	n/a
17	chr12:8171633-8171683	NHDF-neo	bronchial:	n/a
18	chr12:8170797-8170847	PFSK-1	brain:	n/a
19	chr12:8171463-8171513	SK-N-MC	brain:	n/a
20	chr12:8171686-8171736	HAEpiC	amniotic membrane:	n/a
21	chr12:8171463-8171513	AG09319	gingival:	n/a
22	chr12:8167594-8167644	SAEC	small airway:	n/a
23	chr12:8171633-8171683	Caco-2	colon:	n/a
24	chr12:8171686-8171736	LNCaP	prostate:	n/a
25	chr12:8170797-8170847	NH-A	brain:	n/a
26	chr12:8170797-8170847	PANC-1	pancreas:	n/a
27	chr12:8167594-8167644	K562	blood:	n/a
28	chr12:8171633-8171683	SAEC	small airway:	n/a
29	chr12:8167594-8167644	GM12892	blood:	n/a
30	chr12:8170797-8170847	MCF-7	breast:	n/a
31	chr12:8171686-8171736	NH-A	brain:	n/a
32	chr12:8167594-8167644	HCM	heart:	n/a
33	chr12:8170797-8170847	AG10803	skin:	n/a
34	chr12:8167594-8167644	PFSK-1	brain:	n/a
35	chr12:8171463-8171513	AoSMC	blood vessel:	n/a
36	chr12:8171633-8171683	HL-60	blood:	n/a
37	chr12:8170797-8170847	K562	blood:	n/a
38	chr12:8170797-8170847	GM19239	blood:	n/a
39	chr12:8171633-8171683	GM12891	blood:	n/a
40	chr12:8170797-8170847	CMK	blood:	n/a
41	chr12:8167594-8167644	BE2_C	brain:	n/a
42	chr12:8171463-8171513	AG09309	skin:	n/a
43	chr12:8167594-8167644	NB4	blood:	n/a
44	chr12:8170797-8170847	NT2-D1	testis:	n/a
45	chr12:8167594-8167644	CMK	blood:	n/a
46	chr12:8171633-8171683	HEK293	kidney:	embryo
47	chr12:8170797-8170847	BE2_C	brain:	n/a
48	chr12:8171463-8171513	MCF-7	breast:	n/a
49	chr12:8171633-8171683	AG04449	skin:	fetal
50	chr12:8170797-8170847	HUVEC	blood vessel:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:8171182..8172888-chr12:8173729..8176530,2	K562	blood:
2	chr12:8088481..8090137-chr12:8171670..8173575,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3AR1-1	chr12:8168914-8168990	NONHSAT026280
2	lnc-C3AR1-1	chr12:8169003-8169017	NONHSAT026280
3	lnc-C3AR1-1	chr12:8169633-8169667	NONHSAT026280
4	lnc-C3AR1-1	chr12:8169309-8169557	NONHSAT026280
5	lnc-C3AR1-1	chr12:8169691-8169776	NONHSAT026280

No data

Variant related genes	Relation type
ENSG00000255581	TF binding region
ENSG00000255964	TF binding region
ENSG00000255581	CpG island
ENSG00000255964	CpG island
ENSG00000059804	chromatin interactions

Extended variants
information (count: 122 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:122 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547223705	chr12:8166784-8166785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs60311276	chr12:8167059-8167060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371489181	chr12:8167147-8167148	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549798470	chr12:8167222-8167223	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs377240845	chr12:8167306-8167307	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs191789239	chr12:8167321-8167322	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs528365724	chr12:8167338-8167339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200776341	chr12:8167367-8167368	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs148725508	chr12:8167369-8167370	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201008616	chr12:8167370-8167371	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs59361466	chr12:8167371-8167372	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs7958855	chr12:8167383-8167384	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs141220156	chr12:8167397-8167398	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs7975579	chr12:8167401-8167402	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs368300744	chr12:8167406-8167407	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs80052417	chr12:8167411-8167412	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs4242904	chr12:8167412-8167413	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs530694299	chr12:8167524-8167525	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs10744118	chr12:8167541-8167542	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs116107100	chr12:8167594-8167595	Weak transcription Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs4883475	chr12:8167632-8167633	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs150333282	chr12:8167659-8167660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200595718	chr12:8167662-8167663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs61245881	chr12:8167695-8167696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184276855	chr12:8167728-8167729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369866633	chr12:8167761-8167762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112488025	chr12:8167772-8167773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530178149	chr12:8167780-8167781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113921041	chr12:8167802-8167803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189227573	chr12:8167820-8167821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs202003517	chr12:8167854-8167855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4883476	chr12:8167855-8167856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs35720691	chr12:8167909-8167910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371122596	chr12:8167966-8167967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78796870	chr12:8167967-8167968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10846333	chr12:8167995-8167996	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12320769	chr12:8168063-8168064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs569232434	chr12:8168072-8168073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142364090	chr12:8168084-8168085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375806433	chr12:8168178-8168179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538004657	chr12:8168307-8168308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554904381	chr12:8168316-8168317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146016279	chr12:8168317-8168318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370414900	chr12:8168326-8168327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573676161	chr12:8168345-8168346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193223026	chr12:8168381-8168382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545790263	chr12:8168395-8168396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139640515	chr12:8168406-8168407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12303680	chr12:8168436-8168437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs185460719	chr12:8168470-8168471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Lung cancer	18438408	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8158800-8171200	Weak transcription	Gastric	stomach
2	chr12:8163600-8170800	Weak transcription	Fetal Thymus	thymus
3	chr12:8163800-8170200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr12:8165000-8169000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr12:8165800-8170800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr12:8166200-8170200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:8167200-8170200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:8167400-8167600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:8167400-8167600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:8167400-8167600	Bivalent Enhancer	NHEK	skin
11	chr12:8169000-8169600	Enhancers	Primary hematopoietic stem cells	blood
12	chr12:8169600-8171200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:8170200-8170400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr12:8170200-8170400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr12:8170200-8170400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:8170200-8170800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:8170200-8171000	Bivalent Enhancer	Dnd41	blood
18	chr12:8170400-8170800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr12:8170400-8170800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr12:8170400-8170800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:8170600-8170800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:8170800-8171000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:8170800-8171000	Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr12:8170800-8171000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr12:8170800-8171000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
26	chr12:8170800-8171000	Bivalent Enhancer	Fetal Brain Male	brain
27	chr12:8170800-8171000	Enhancers	Fetal Thymus	thymus
28	chr12:8170800-8171000	Enhancers	Thymus	Thymus
29	chr12:8170800-8171200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr12:8170800-8171200	Enhancers	Primary hematopoietic stem cells	blood
31	chr12:8170800-8171200	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr12:8170800-8171200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
33	chr12:8170800-8171400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
34	chr12:8170800-8171400	Bivalent Enhancer	Placenta	Placenta
35	chr12:8170800-8171400	Active TSS	Psoas Muscle	Psoas
36	chr12:8170800-8171600	Enhancers	Lung	lung
37	chr12:8170800-8172000	Active TSS	HUES64 Cell Line	embryonic stem cell
38	chr12:8170800-8172000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr12:8170800-8172200	Active TSS	H1 Cell Line	embryonic stem cell
40	chr12:8170800-8172200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr12:8170800-8172200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:8170800-8172200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:8170800-8172400	Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr12:8171000-8171200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:8171000-8171200	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr12:8171000-8171200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:8171000-8171200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
48	chr12:8171000-8171200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
49	chr12:8171000-8171200	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
50	chr12:8171000-8171200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links