Variant report

Variant	esv3383633
Chromosome Location	chr12:7809549-7827817
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	chr12:7819304-7819445	HepG2	liver:	n/a	n/a
2	CTCF	chr12:7819729-7820192	MCF-7	breast:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
3	CTCF	chr12:7820200-7820350	AG04449	skin:	n/a	n/a
4	CTCF	chr12:7819840-7819990	HRPEpiC	eye:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
5	CTCF	chr12:7819820-7819970	NHDF-neo	bronchial:	n/a	n/a
6	CTCF	chr12:7820700-7820850	GM06990	blood:	n/a	n/a
7	CTCF	chr12:7819960-7820110	GM12866	blood:	n/a	chr12:7819966-7819974
8	CTCF	chr12:7819860-7820010	HCPEpiC	choroid plexus:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
9	CTCF	chr12:7819820-7819970	HMEC	breast:	n/a	n/a
10	CTCF	chr12:7819760-7819910	GM12867	blood:	n/a	n/a
11	CTCF	chr12:7819920-7820070	K562	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
12	CTCF	chr12:7819840-7819990	HCM	heart:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
13	CTCF	chr12:7819840-7819990	HFF	foreskin:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
14	CTCF	chr12:7819860-7820010	HUVEC	blood vessel:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
15	CTCF	chr12:7820020-7820170	NHLF	lung:	n/a	n/a
16	CTCF	chr12:7819860-7820010	HepG2	liver:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
17	CTCF	chr12:7819860-7820010	GM12869	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
18	CTCF	chr12:7819840-7819990	GM12867	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
19	CTCF	chr12:7819841-7820023	HepG2	liver:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
20	CTCF	chr12:7819850-7820132	GM12878	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
21	CTCF	chr12:7819838-7820159	H1-hESC	embryonic stem cell:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
22	CTCF	chr12:7819860-7820010	GM12873	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
23	CTCF	chr12:7819900-7820050	HMEC	breast:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
24	CTCF	chr12:7820100-7820250	K562	blood:	n/a	n/a
25	CTCF	chr12:7819720-7819870	RPTEC	kidney:	n/a	n/a
26	CTCF	chr12:7819800-7819950	HEK293	kidney:	n/a	n/a
27	CTCF	chr12:7819904-7820037	ProgFib	skin:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
28	CTCF	chr12:7819840-7819990	HFF-Myc	foreskin:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
29	CTCF	chr12:7819860-7820010	GM06990	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
30	CTCF	chr12:7819930-7820014	GM13977	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
31	CTCF	chr12:7819900-7820050	BJ	skin:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
32	CTCF	chr12:7819940-7820090	BE2_C	brain:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
33	CTCF	chr12:7819662-7820324	A549	lung:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
34	CTCF	chr12:7819880-7820030	RPTEC	kidney:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
35	CTCF	chr12:7819900-7820050	AG04449	skin:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
36	CTCF	chr12:7819925-7820012	LNCaP	prostate:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
37	CTCF	chr12:7819860-7820010	GM12878	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
38	CTCF	chr12:7819920-7820070	GM06990	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
39	CTCF	chr12:7819784-7820078	A549	lung:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
40	CTCF	chr12:7819920-7820070	A549	lung:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
41	CTCF	chr12:7819900-7820050	Caco-2	colon:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
42	CTCF	chr12:7819880-7820030	AG09319	gingival:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
43	CTCF	chr12:7819960-7820110	GM12867	blood:	n/a	chr12:7819966-7819974
44	CTCF	chr12:7819840-7819990	GM12870	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
45	CTCF	chr12:7819880-7820030	AG09309	skin:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
46	CTCF	chr12:7819940-7820090	GM12865	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
47	CTCF	chr12:7819900-7820050	HL-60	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
48	CTCF	chr12:7819860-7820010	GM12864	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
49	CTCF	chr12:7819860-7820010	HPAF	blood vessel:	n/a	chr12:7819956-7819977 chr12:7819966-7819974
50	CTCF	chr12:7819880-7820030	K562	blood:	n/a	chr12:7819956-7819977 chr12:7819966-7819974

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:7819180-7819230	SAEC	small airway:	n/a
2	chr12:7818654-7818704	AoSMC	blood vessel:	n/a
3	chr12:7818654-7818704	HAEpiC	amniotic membrane:	n/a
4	chr12:7818635-7818685	AG04450	lung:	fetal
5	chr12:7818654-7818704	SAEC	small airway:	n/a
6	chr12:7818585-7818635	ovcar-3	ovarian:	n/a
7	chr12:7818585-7818635	Hepatocyte	liver:	n/a
8	chr12:7818635-7818685	GM12878	blood:	n/a
9	chr12:7818585-7818635	HIPEpiC	eye:	n/a
10	chr12:7818635-7818685	H1-hESC	embryonic stem cell:	embryo
11	chr12:7818654-7818704	Jurkat	blood:	n/a
12	chr12:7818635-7818685	HepG2	liver:	n/a
13	chr12:7818585-7818635	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:7818585-7818635	NHBE	bronchial:	n/a
15	chr12:7818654-7818704	MCF-7	breast:	n/a
16	chr12:7817844-7817894	PFSK-1	brain:	n/a
17	chr12:7819180-7819230	SK-N-MC	brain:	n/a
18	chr12:7819180-7819230	Jurkat	blood:	n/a
19	chr12:7818654-7818704	SK-N-MC	brain:	n/a
20	chr12:7818585-7818635	MCF10A-Er-Src	breast:	n/a
21	chr12:7818635-7818685	RPTEC	kidney:	n/a
22	chr12:7818585-7818635	AG04449	skin:	fetal
23	chr12:7819180-7819230	CMK	blood:	n/a
24	chr12:7817844-7817894	HUVEC	blood vessel:	n/a
25	chr12:7819180-7819230	T-47D	breast:	n/a
26	chr12:7819180-7819230	MCF10A-Er-Src	breast:	n/a
27	chr12:7817844-7817894	GM19239	blood:	n/a
28	chr12:7818585-7818635	CMK	blood:	n/a
29	chr12:7818585-7818635	AG09319	gingival:	n/a
30	chr12:7819180-7819230	A549	lung:	n/a
31	chr12:7819180-7819230	HEK293	kidney:	embryo
32	chr12:7818585-7818635	AG04450	lung:	fetal
33	chr12:7818635-7818685	HCT-116	colon:	n/a
34	chr12:7818585-7818635	SK-N-SH_RA	brain:	n/a
35	chr12:7818585-7818635	BE2_C	brain:	n/a
36	chr12:7818585-7818635	AG09309	skin:	n/a
37	chr12:7818635-7818685	GM19239	blood:	n/a
38	chr12:7818585-7818635	HL-60	blood:	n/a
39	chr12:7819180-7819230	HCF	heart:	n/a
40	chr12:7818635-7818685	HEK293	kidney:	embryo
41	chr12:7818635-7818685	NB4	blood:	n/a
42	chr12:7817844-7817894	SKMC	muscle:	n/a
43	chr12:7818635-7818685	HRCEpiC	kidney:	n/a
44	chr12:7817844-7817894	HNPCEpiC	eye:	n/a
45	chr12:7819180-7819230	HIPEpiC	eye:	n/a
46	chr12:7817844-7817894	HRE	kidney:	n/a
47	chr12:7819180-7819230	ProgFib	skin:	n/a
48	chr12:7818654-7818704	AG09319	gingival:	n/a
49	chr12:7817844-7817894	BE2_C	brain:	n/a
50	chr12:7818635-7818685	IMR90	lung:	fetal

Variant related genes	Relation type
APOBEC1	TF binding region
APOBEC1	CpG island

Extended variants
information (count: 470 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370562111	chr12:7809640-7809641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200166836	chr12:7809650-7809651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200766623	chr12:7809651-7809652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs71038711	chr12:7809666-7809667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150878247	chr12:7809766-7809767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576783571	chr12:7809787-7809788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375386279	chr12:7809791-7809792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562365180	chr12:7809810-7809811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138447587	chr12:7809944-7809945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531601482	chr12:7809985-7809986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192265760	chr12:7809996-7809997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182926239	chr12:7810050-7810051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77593165	chr12:7810091-7810092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145746177	chr12:7810171-7810172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3040824	chr12:7810173-7810174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201786831	chr12:7810174-7810175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201025328	chr12:7810180-7810181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76818788	chr12:7810183-7810184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187644053	chr12:7810248-7810249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576651571	chr12:7810283-7810284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1015102	chr12:7810299-7810300	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs373290045	chr12:7810306-7810307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534020874	chr12:7810449-7810450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562299007	chr12:7810515-7810516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12314594	chr12:7810558-7810559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566912357	chr12:7810586-7810587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149281343	chr12:7810610-7810611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368668184	chr12:7810634-7810635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs151074476	chr12:7810641-7810642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370722017	chr12:7810642-7810643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75339711	chr12:7810678-7810679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560305012	chr12:7810711-7810712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535599950	chr12:7810743-7810744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73064650	chr12:7810750-7810751	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs192519174	chr12:7810763-7810764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61937007	chr12:7810767-7810768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184839350	chr12:7810821-7810822	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575271737	chr12:7810839-7810840	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112700769	chr12:7810853-7810854	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568796144	chr12:7810949-7810950	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188918376	chr12:7810955-7810956	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192202977	chr12:7810990-7810991	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531628260	chr12:7811003-7811004	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139124685	chr12:7811021-7811022	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548238227	chr12:7811198-7811199	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144001960	chr12:7811294-7811295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113348556	chr12:7811333-7811334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139977087	chr12:7811361-7811362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142142133	chr12:7811432-7811433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184675243	chr12:7811436-7811437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
small cell lung cancer	20016488	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
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Nasopharyngeal cancer	20548289	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7798800-7815200	Weak transcription	Duodenum Mucosa	Duodenum
2	chr12:7807400-7810000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr12:7808200-7809600	Enhancers	Fetal Intestine Large	intestine
4	chr12:7808800-7810800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:7808800-7811000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr12:7808800-7812200	Enhancers	Primary hematopoietic stem cells	blood
7	chr12:7808800-7812400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:7809000-7809600	Enhancers	Fetal Intestine Small	intestine
9	chr12:7809200-7811600	Enhancers	Primary B cells from peripheral blood	blood
10	chr12:7809600-7817200	Weak transcription	Fetal Intestine Small	intestine
11	chr12:7810000-7810400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr12:7810600-7811200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr12:7810800-7811200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:7811200-7812400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:7812000-7812200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr12:7815200-7815600	Enhancers	Duodenum Mucosa	Duodenum
17	chr12:7815600-7817600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr12:7817200-7817400	Flanking Active TSS	Fetal Intestine Small	intestine
19	chr12:7817400-7817600	Enhancers	Fetal Intestine Large	intestine
20	chr12:7817400-7817600	Enhancers	Stomach Mucosa	stomach
21	chr12:7817400-7818400	Active TSS	Fetal Intestine Small	intestine
22	chr12:7817600-7818200	Active TSS	Fetal Intestine Large	intestine
23	chr12:7817600-7818600	Weak transcription	Stomach Mucosa	stomach
24	chr12:7817600-7818800	Active TSS	Duodenum Mucosa	Duodenum
25	chr12:7818200-7818400	Weak transcription	Fetal Intestine Large	intestine
26	chr12:7818400-7818600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr12:7818400-7819000	Weak transcription	Fetal Intestine Small	intestine
28	chr12:7818400-7820000	Enhancers	HepG2	liver
29	chr12:7818400-7820400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr12:7818400-7821600	Enhancers	Fetal Intestine Large	intestine
31	chr12:7818600-7818800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:7818600-7819200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr12:7818600-7819400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr12:7818600-7820000	Enhancers	Stomach Mucosa	stomach
35	chr12:7818800-7819800	Weak transcription	Duodenum Mucosa	Duodenum
36	chr12:7819000-7819200	Enhancers	Fetal Intestine Small	intestine
37	chr12:7819000-7820200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:7819200-7819400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr12:7819200-7819600	Weak transcription	Fetal Intestine Small	intestine
40	chr12:7819200-7820400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:7819600-7821400	Enhancers	Fetal Intestine Small	intestine
42	chr12:7819800-7821400	Enhancers	Duodenum Mucosa	Duodenum
43	chr12:7820200-7820800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:7820400-7820800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr12:7824200-7846000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:7827000-7828800	Enhancers	Primary B cells from cord blood	blood
47	chr12:7827000-7828800	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr12:7827000-7831200	Enhancers	Primary hematopoietic stem cells	blood
49	chr12:7827000-7832600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:7827200-7829600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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