Variant report

Variant	nsv556865
Chromosome Location	chr12:295367-298500
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	chr12:298349-298388	K562	blood:	n/a	n/a
2	BHLHE40	chr12:298401-298467	K562	blood:	n/a	n/a
3	BHLHE40	chr12:298253-298607	HepG2	liver:	n/a	n/a
4	BRCA1	chr12:298216-298256	HepG2	liver:	n/a	n/a
5	CCNT2	chr12:298259-298565	K562	blood:	n/a	n/a
6	CEBPD	chr12:298272-298550	HepG2	liver:	n/a	n/a
7	CHD2	chr12:298159-298475	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr12:298202-298629	A549	lung:	n/a	n/a
9	CTCF	chr12:296060-296210	A549	lung:	n/a	chr12:296091-296112 chr12:296096-296114 chr12:296098-296111
10	CTCF	chr12:298200-298630	K562	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
11	CTCF	chr12:298420-298570	HBMEC	blood vessel:	n/a	chr12:298430-298443 chr12:298428-298446
12	CTCF	chr12:298172-298614	H1-hESC	embryonic stem cell:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
13	CTCF	chr12:298186-298673	A549	lung:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
14	CTCF	chr12:298313-298577	Pancreas_OC	pancreas:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
15	CTCF	chr12:298380-298530	HFF-Myc	foreskin:	n/a	chr12:298430-298443 chr12:298428-298446
16	CTCF	chr12:298380-298530	HRE	kidney:	n/a	chr12:298430-298443 chr12:298428-298446
17	CTCF	chr12:298380-298530	A549	lung:	n/a	chr12:298430-298443 chr12:298428-298446
18	CTCF	chr12:298360-298510	GM12873	blood:	n/a	chr12:298430-298443 chr12:298428-298446
19	CTCF	chr12:298400-298550	GM12873	blood:	n/a	chr12:298430-298443 chr12:298428-298446
20	CTCF	chr12:298325-298558	GM19240	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
21	CTCF	chr12:298360-298510	HEEpiC	esophagus:	n/a	chr12:298430-298443 chr12:298428-298446
22	CTCF	chr12:298380-298530	HCPEpiC	choroid plexus:	n/a	chr12:298430-298443 chr12:298428-298446
23	CTCF	chr12:298360-298510	GM12872	blood:	n/a	chr12:298430-298443 chr12:298428-298446
24	CTCF	chr12:298231-298533	T-47D	breast:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
25	CTCF	chr12:298440-298590	GM06990	blood:	n/a	n/a
26	CTCF	chr12:298120-298270	NHEK	skin:	n/a	n/a
27	CTCF	chr12:298308-298532	GM20000	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
28	CTCF	chr12:298440-298590	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr12:298420-298570	Caco-2	colon:	n/a	chr12:298430-298443 chr12:298428-298446
30	CTCF	chr12:298301-298568	GM12892	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
31	CTCF	chr12:298400-298550	HUVEC	blood vessel:	n/a	chr12:298430-298443 chr12:298428-298446
32	CTCF	chr12:298318-298552	Lung_OC	lung:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
33	CTCF	chr12:298380-298530	HVMF	connective:	n/a	chr12:298430-298443 chr12:298428-298446
34	CTCF	chr12:298251-298627	K562	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
35	CTCF	chr12:298298-298577	GM19238	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
36	CTCF	chr12:298400-298550	HMF	breast:	n/a	chr12:298430-298443 chr12:298428-298446
37	CTCF	chr12:298360-298510	HRPEpiC	eye:	n/a	chr12:298430-298443 chr12:298428-298446
38	CTCF	chr12:298380-298530	HUVEC	blood vessel:	n/a	chr12:298430-298443 chr12:298428-298446
39	CTCF	chr12:298280-298430	A549	lung:	n/a	chr12:298350-298363
40	CTCF	chr12:298420-298570	GM12864	blood:	n/a	chr12:298430-298443 chr12:298428-298446
41	CTCF	chr12:298400-298550	AG10803	skin:	n/a	chr12:298430-298443 chr12:298428-298446
42	CTCF	chr12:298380-298530	GM12870	blood:	n/a	chr12:298430-298443 chr12:298428-298446
43	CTCF	chr12:298400-298550	GM12868	blood:	n/a	chr12:298430-298443 chr12:298428-298446
44	CTCF	chr12:295997-296216	HepG2	liver:	n/a	chr12:296091-296112 chr12:296096-296114 chr12:296098-296111
45	CTCF	chr12:298360-298510	GM12874	blood:	n/a	chr12:298430-298443 chr12:298428-298446
46	CTCF	chr12:298400-298550	HRPEpiC	eye:	n/a	chr12:298430-298443 chr12:298428-298446
47	CTCF	chr12:298325-298575	ProgFib	skin:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
48	CTCF	chr12:298118-298203	GM12891	blood:	n/a	n/a
49	CTCF	chr12:298360-298510	RPTEC	kidney:	n/a	chr12:298430-298443 chr12:298428-298446
50	CTCF	chr12:298400-298550	HPF	lung:	n/a	chr12:298430-298443 chr12:298428-298446

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:296540-296590	HCT-116	colon:	n/a
2	chr12:297356-297406	HUVEC	blood vessel:	n/a
3	chr12:296540-296590	HCT-116	colon:	n/a
4	chr12:297356-297406	HUVEC	blood vessel:	n/a
5	chr12:298268-298318	HAEpiC	amniotic membrane:	n/a
6	chr12:298484-298534	HAEpiC	amniotic membrane:	n/a
7	chr12:298484-298534	K562	blood:	n/a
8	chr12:298484-298534	PFSK-1	brain:	n/a
9	chr12:298484-298534	U87	brain:	n/a
10	chr12:295951-296001	HNPCEpiC	eye:	n/a
11	chr12:296609-296659	PrEC	prostate:	n/a
12	chr12:298378-298428	H1-hESC	embryonic stem cell:	embryo
13	chr12:296473-296523	HUVEC	blood vessel:	n/a
14	chr12:297831-297881	NHBE	bronchial:	n/a
15	chr12:296540-296590	NT2-D1	testis:	n/a
16	chr12:297356-297406	PrEC	prostate:	n/a
17	chr12:297831-297881	HUVEC	blood vessel:	n/a
18	chr12:298151-298201	GM19239	blood:	n/a
19	chr12:297831-297881	HEK293	kidney:	embryo
20	chr12:297356-297406	NT2-D1	testis:	n/a
21	chr12:298378-298428	SK-N-SH_RA	brain:	n/a
22	chr12:295951-296001	ProgFib	skin:	n/a
23	chr12:297831-297881	Jurkat	blood:	n/a
24	chr12:298378-298428	AG09309	skin:	n/a
25	chr12:296609-296659	HRPEpiC	eye:	n/a
26	chr12:298268-298318	RPTEC	kidney:	n/a
27	chr12:298484-298534	SKMC	muscle:	n/a
28	chr12:297356-297406	SK-N-MC	brain:	n/a
29	chr12:296473-296523	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:298378-298428	HepG2	liver:	n/a
31	chr12:297831-297881	A549	lung:	n/a
32	chr12:298151-298201	Jurkat	blood:	n/a
33	chr12:298151-298201	HRCEpiC	kidney:	n/a
34	chr12:296540-296590	H1-hESC	embryonic stem cell:	embryo
35	chr12:298484-298534	BJ	skin:	n/a
36	chr12:297356-297406	HCF	heart:	n/a
37	chr12:298484-298534	AG04449	skin:	fetal
38	chr12:297831-297881	ECC-1	luminal epithelium:	n/a
39	chr12:298378-298428	NHBE	bronchial:	n/a
40	chr12:297356-297406	H1-hESC	embryonic stem cell:	embryo
41	chr12:295951-296001	NB4	blood:	n/a
42	chr12:297356-297406	Hela-S3	cervix:	n/a
43	chr12:296473-296523	Jurkat	blood:	n/a
44	chr12:298378-298428	SAEC	small airway:	n/a
45	chr12:298268-298318	ProgFib	skin:	n/a
46	chr12:296540-296590	HL-60	blood:	n/a
47	chr12:296473-296523	AG09319	gingival:	n/a
48	chr12:296540-296590	SK-N-SH	brain:	n/a
49	chr12:295951-296001	NT2-D1	testis:	n/a
50	chr12:295951-296001	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:296668..298848-chr12:310032..311975,2	K562	blood:
2	chr12:297943..299013-chr12:328724..329295,3	K562	blood:
3	chr12:297965..298734-chr12:308100..308686,2	MCF-7	breast:
4	chr12:211691..214245-chr12:294558..297175,2	K562	blood:
5	chr12:297600..300406-chr12:301338..304265,4	K562	blood:
6	chr12:298095..299012-chr12:328485..329986,6	MCF-7	breast:
7	chr12:297600..300406-chr12:301639..304265,3	K562	blood:

Variant related genes	Relation type
ENSG00000256540	TF binding region
ENSG00000255671	TF binding region
ENSG00000256540	CpG island
ENSG00000255671	CpG island
ENSG00000255671	chromatin interactions
ENSG00000111181	chromatin interactions

Extended variants
information (count: 258 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs647001	chr12:295367-295368	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117035203	chr12:295368-295369	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs529198	chr12:295370-295371	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs113211320	chr12:295388-295389	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs146465670	chr12:295391-295392	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs564097319	chr12:295392-295393	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs187851664	chr12:295414-295415	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs531313944	chr12:295420-295421	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs191972193	chr12:295438-295439	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs183887068	chr12:295451-295452	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs188427907	chr12:295452-295453	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs797738	chr12:295474-295475	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573373864	chr12:295483-295484	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs797739	chr12:295488-295489	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs140862220	chr12:295492-295493	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs192032620	chr12:295509-295510	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs544306701	chr12:295513-295514	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs478520	chr12:295525-295526	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs478455	chr12:295546-295547	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs527976857	chr12:295547-295548	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs77827781	chr12:295560-295561	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs113413543	chr12:295563-295564	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs7960464	chr12:295585-295586	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs477676	chr12:295588-295589	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs116193589	chr12:295589-295590	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs184437541	chr12:295599-295600	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs477623	chr12:295606-295607	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs143017890	chr12:295625-295626	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550640613	chr12:295632-295633	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568935063	chr12:295635-295636	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138362815	chr12:295643-295644	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115007083	chr12:295690-295691	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111947809	chr12:295697-295698	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs534214251	chr12:295698-295699	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs114062770	chr12:295702-295703	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs550221863	chr12:295712-295713	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs187309990	chr12:295737-295738	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555825169	chr12:295755-295756	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs191757633	chr12:295759-295760	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs377349384	chr12:295765-295766	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs577720319	chr12:295767-295768	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs568280073	chr12:295768-295769	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs535684218	chr12:295773-295774	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs369239786	chr12:295778-295779	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs559888977	chr12:295781-295782	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs527624954	chr12:295784-295785	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs184545129	chr12:295790-295791	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560778816	chr12:295795-295796	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs554003645	chr12:295797-295798	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs543083933	chr12:295801-295802	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	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
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Autism	22495309	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:286200-295800	Weak transcription	Liver	Liver
2	chr12:286200-298000	Weak transcription	Gastric	stomach
3	chr12:288400-297800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:288800-297200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:289200-297800	Weak transcription	Brain Anterior Caudate	brain
6	chr12:289600-298200	Weak transcription	HSMMtube	muscle
7	chr12:290000-297800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr12:290000-297800	Weak transcription	HUVEC	blood vessel
9	chr12:290000-298000	Weak transcription	Esophagus	oesophagus
10	chr12:290200-297800	Weak transcription	Brain Hippocampus Middle	brain
11	chr12:291200-297600	Weak transcription	Pancreas	Pancrea
12	chr12:292000-297200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr12:292000-297600	Weak transcription	Right Ventricle	heart
14	chr12:292000-298200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr12:292600-298000	Weak transcription	NH-A	brain
16	chr12:292800-297800	Weak transcription	Left Ventricle	heart
17	chr12:294200-295400	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr12:294400-295600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr12:294600-295400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:294600-298000	Weak transcription	HSMM	muscle
21	chr12:294800-296400	Enhancers	Fetal Muscle Leg	muscle
22	chr12:295000-296000	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr12:295000-297800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr12:295000-297800	Weak transcription	Adipose Nuclei	Adipose
25	chr12:295200-296200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr12:295200-297600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr12:295200-297600	Weak transcription	Spleen	Spleen
28	chr12:295200-298200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr12:295400-297600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:295400-298000	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr12:295600-296000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:295800-297800	Enhancers	Liver	Liver
33	chr12:296000-296200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:296000-296200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
35	chr12:296200-296600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:296200-297800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr12:296400-296800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:296600-296800	Bivalent Enhancer	K562	blood
39	chr12:296600-298000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr12:296800-297800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr12:297200-297400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr12:297200-297800	Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr12:297200-298400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr12:297200-298600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr12:297400-297600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:297400-297800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr12:297400-298400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr12:297400-298400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr12:297600-297800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:297600-297800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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