Variant report

Variant	nsv556860
Chromosome Location	chr12:293513-298500
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	chr12:294691-295034	K562	blood:	n/a	chr12:294869-294878 chr12:294870-294879 chr12:294867-294880 chr12:294868-294877 chr12:294869-294878
3	BHLHE40	chr12:294714-295081	HepG2	liver:	n/a	chr12:294869-294878 chr12:294870-294879 chr12:294867-294880 chr12:294868-294877 chr12:294869-294878
4	BHLHE40	chr12:298253-298607	HepG2	liver:	n/a	n/a
5	BHLHE40	chr12:298401-298467	K562	blood:	n/a	n/a
6	BRCA1	chr12:298216-298256	HepG2	liver:	n/a	n/a
7	CCNT2	chr12:298259-298565	K562	blood:	n/a	n/a
8	CEBPD	chr12:298272-298550	HepG2	liver:	n/a	n/a
9	CHD2	chr12:298159-298475	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr12:298202-298629	A549	lung:	n/a	n/a
11	CTCF	chr12:298400-298550	GM12878	blood:	n/a	chr12:298430-298443 chr12:298428-298446
12	CTCF	chr12:298120-298270	HRPEpiC	eye:	n/a	n/a
13	CTCF	chr12:298340-298490	AG04450	lung:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
14	CTCF	chr12:298360-298510	BE2_C	brain:	n/a	chr12:298430-298443 chr12:298428-298446
15	CTCF	chr12:298293-298558	GM10248	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
16	CTCF	chr12:298290-298566	MCF-7	breast:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
17	CTCF	chr12:298400-298550	AG09309	skin:	n/a	chr12:298430-298443 chr12:298428-298446
18	CTCF	chr12:298360-298510	WI-38	lung:	n/a	chr12:298430-298443 chr12:298428-298446
19	CTCF	chr12:298360-298510	HFF-Myc	foreskin:	n/a	chr12:298430-298443 chr12:298428-298446
20	CTCF	chr12:298312-298592	Gliobla	brain:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
21	CTCF	chr12:298380-298530	RPTEC	kidney:	n/a	chr12:298430-298443 chr12:298428-298446
22	CTCF	chr12:298193-298744	K562	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
23	CTCF	chr12:298325-298558	GM19240	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
24	CTCF	chr12:298380-298530	MCF-7	breast:	n/a	chr12:298430-298443 chr12:298428-298446
25	CTCF	chr12:298380-298530	GM12870	blood:	n/a	chr12:298430-298443 chr12:298428-298446
26	CTCF	chr12:298400-298550	HPF	lung:	n/a	chr12:298430-298443 chr12:298428-298446
27	CTCF	chr12:297806-297874	GM19239	blood:	n/a	n/a
28	CTCF	chr12:298380-298530	AG04449	skin:	n/a	chr12:298430-298443 chr12:298428-298446
29	CTCF	chr12:298236-298587	T-47D	breast:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
30	CTCF	chr12:298400-298550	NHLF	lung:	n/a	chr12:298430-298443 chr12:298428-298446
31	CTCF	chr12:298360-298510	HRPEpiC	eye:	n/a	chr12:298430-298443 chr12:298428-298446
32	CTCF	chr12:298400-298550	AG10803	skin:	n/a	chr12:298430-298443 chr12:298428-298446
33	CTCF	chr12:298309-298578	LNCaP	prostate:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
34	CTCF	chr12:298440-298590	GM06990	blood:	n/a	n/a
35	CTCF	chr12:298380-298530	GM12874	blood:	n/a	chr12:298430-298443 chr12:298428-298446
36	CTCF	chr12:298302-298499	ECC-1	luminal epithelium:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
37	CTCF	chr12:298400-298550	HEK293	kidney:	n/a	chr12:298430-298443 chr12:298428-298446
38	CTCF	chr12:298120-298270	AG04449	skin:	n/a	n/a
39	CTCF	chr12:298318-298565	GM13977	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
40	CTCF	chr12:297870-299146	SK-N-SH	brain:	n/a	chr12:298430-298443 chr12:299002-299012 chr12:298428-298446 chr12:298350-298363
41	CTCF	chr12:298380-298530	AG10803	skin:	n/a	chr12:298430-298443 chr12:298428-298446
42	CTCF	chr12:298380-298530	SAEC	small airway:	n/a	chr12:298430-298443 chr12:298428-298446
43	CTCF	chr12:296689-296843	K562	blood:	n/a	n/a
44	CTCF	chr12:298420-298570	BJ	skin:	n/a	chr12:298430-298443 chr12:298428-298446
45	CTCF	chr12:298400-298550	GM12864	blood:	n/a	chr12:298430-298443 chr12:298428-298446
46	CTCF	chr12:298400-298550	SAEC	small airway:	n/a	chr12:298430-298443 chr12:298428-298446
47	CTCF	chr12:298360-298510	HEEpiC	esophagus:	n/a	chr12:298430-298443 chr12:298428-298446
48	CTCF	chr12:298280-298583	MCF-7	breast:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
49	CTCF	chr12:298440-298590	GM12870	blood:	n/a	n/a
50	CTCF	chr12:298400-298550	GM12866	blood:	n/a	chr12:298430-298443 chr12:298428-298446

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:298268-298318	HCF	heart:	n/a
2	chr12:298268-298318	HCF	heart:	n/a
3	chr12:298378-298428	HMEC	breast:	n/a
4	chr12:296540-296590	CMK	blood:	n/a
5	chr12:298268-298318	GM19239	blood:	n/a
6	chr12:297831-297881	HRPEpiC	eye:	n/a
7	chr12:296540-296590	AG09309	skin:	n/a
8	chr12:295951-296001	HRPEpiC	eye:	n/a
9	chr12:298484-298534	GM12891	blood:	n/a
10	chr12:298378-298428	HRPEpiC	eye:	n/a
11	chr12:295951-296001	H1-hESC	embryonic stem cell:	embryo
12	chr12:296540-296590	A549	lung:	n/a
13	chr12:297831-297881	PFSK-1	brain:	n/a
14	chr12:295951-296001	T-47D	breast:	n/a
15	chr12:298378-298428	BJ	skin:	n/a
16	chr12:297356-297406	AoSMC	blood vessel:	n/a
17	chr12:296609-296659	BE2_C	brain:	n/a
18	chr12:297356-297406	HepG2	liver:	n/a
19	chr12:296540-296590	HCPEpiC	choroid plexus:	n/a
20	chr12:297831-297881	MCF-7	breast:	n/a
21	chr12:295951-296001	NT2-D1	testis:	n/a
22	chr12:296540-296590	U87	brain:	n/a
23	chr12:298151-298201	PFSK-1	brain:	n/a
24	chr12:296540-296590	HNPCEpiC	eye:	n/a
25	chr12:296473-296523	NB4	blood:	n/a
26	chr12:297356-297406	HRCEpiC	kidney:	n/a
27	chr12:298151-298201	GM12878	blood:	n/a
28	chr12:298378-298428	SK-N-SH	brain:	n/a
29	chr12:298378-298428	SK-N-MC	brain:	n/a
30	chr12:295951-296001	GM12892	blood:	n/a
31	chr12:297356-297406	HUVEC	blood vessel:	n/a
32	chr12:295951-296001	PrEC	prostate:	n/a
33	chr12:297831-297881	SK-N-SH	brain:	n/a
34	chr12:298151-298201	K562	blood:	n/a
35	chr12:298268-298318	HEK293	kidney:	embryo
36	chr12:295951-296001	AG09309	skin:	n/a
37	chr12:295951-296001	MCF10A-Er-Src	breast:	n/a
38	chr12:296609-296659	K562	blood:	n/a
39	chr12:296473-296523	A549	lung:	n/a
40	chr12:296540-296590	HEEpiC	esophagus:	n/a
41	chr12:298151-298201	MCF10A-Er-Src	breast:	n/a
42	chr12:295951-296001	NHBE	bronchial:	n/a
43	chr12:298378-298428	AG09319	gingival:	n/a
44	chr12:298268-298318	HCT-116	colon:	n/a
45	chr12:298151-298201	HepG2	liver:	n/a
46	chr12:297831-297881	Hepatocyte	liver:	n/a
47	chr12:295951-296001	HEK293	kidney:	embryo
48	chr12:297831-297881	SK-N-MC	brain:	n/a
49	chr12:298151-298201	NHDF-neo	bronchial:	n/a
50	chr12:298268-298318	BE2_C	brain:	n/a

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

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

Extended variants
information (count: 402 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:402 , 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	rs183355	chr12:293513-293514	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547140775	chr12:293516-293517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559277202	chr12:293557-293558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527825300	chr12:293588-293589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549192215	chr12:293612-293613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188361632	chr12:293625-293626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs797736	chr12:293626-293627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs550512873	chr12:293637-293638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571928757	chr12:293650-293651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539239718	chr12:293654-293655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554456677	chr12:293655-293656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111450898	chr12:293669-293670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536382515	chr12:293685-293686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554348979	chr12:293687-293688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs797737	chr12:293688-293689	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs542972528	chr12:293691-293692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186035126	chr12:293692-293693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576771745	chr12:293698-293699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540917809	chr12:293713-293714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368786359	chr12:293727-293728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199640970	chr12:293730-293731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190558330	chr12:293733-293734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113258975	chr12:293743-293744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1212459	chr12:293744-293745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548255845	chr12:293758-293759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369514919	chr12:293773-293774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11061810	chr12:293774-293775	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182394594	chr12:293784-293785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532899360	chr12:293785-293786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547759892	chr12:293786-293787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186774924	chr12:293787-293788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536420001	chr12:293809-293810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554656684	chr12:293841-293842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569363647	chr12:293859-293860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143022706	chr12:293873-293874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190345923	chr12:293885-293886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551130133	chr12:293894-293895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540954865	chr12:293895-293896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373525627	chr12:293903-293904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182585581	chr12:293910-293911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574591393	chr12:293911-293912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200617021	chr12:293918-293919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374817036	chr12:293929-293930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112106594	chr12:293933-293934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561436832	chr12:293961-293962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531888284	chr12:293999-294000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185358073	chr12:294018-294019	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs113856433	chr12:294021-294022	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs532530795	chr12:294063-294064	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs118164264	chr12:294071-294072	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	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:285 , 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	chr12:288400-295200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:288400-297800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:288800-297200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:289200-297800	Weak transcription	Brain Anterior Caudate	brain
7	chr12:289600-298200	Weak transcription	HSMMtube	muscle
8	chr12:290000-297800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr12:290000-297800	Weak transcription	HUVEC	blood vessel
10	chr12:290000-298000	Weak transcription	Esophagus	oesophagus
11	chr12:290200-297800	Weak transcription	Brain Hippocampus Middle	brain
12	chr12:291200-297600	Weak transcription	Pancreas	Pancrea
13	chr12:291600-294400	Weak transcription	Spleen	Spleen
14	chr12:291800-294200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr12:292000-294000	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr12:292000-294000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr12:292000-294200	Weak transcription	Placenta	Placenta
18	chr12:292000-294200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr12:292000-297200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr12:292000-297600	Weak transcription	Right Ventricle	heart
21	chr12:292000-298200	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr12:292200-294000	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr12:292200-294400	Weak transcription	HSMM	muscle
24	chr12:292400-293800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:292600-298000	Weak transcription	NH-A	brain
26	chr12:292800-294400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:292800-297800	Weak transcription	Left Ventricle	heart
28	chr12:293400-295200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr12:293800-294000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:294000-294200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:294000-294400	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr12:294000-294600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr12:294000-294800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr12:294200-294400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:294200-295000	Enhancers	Primary hematopoietic stem cells	blood
36	chr12:294200-295000	Enhancers	Adipose Nuclei	Adipose
37	chr12:294200-295000	Enhancers	Placenta	Placenta
38	chr12:294200-295400	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr12:294400-294600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:294400-294600	Enhancers	Lung	lung
41	chr12:294400-294600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr12:294400-294600	Enhancers	HSMM	muscle
43	chr12:294400-295000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr12:294400-295200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr12:294400-295200	Enhancers	Spleen	Spleen
46	chr12:294400-295600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr12:294600-294800	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr12:294600-295400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:294600-298000	Weak transcription	HSMM	muscle
50	chr12:294800-295000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle

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