Variant report

Variant	nsv898855
Chromosome Location	chr12:20278430-20354786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:20328706-20329235	HepG2	liver:	n/a	n/a
2	ATF2	chr12:20297246-20297708	GM12878	blood:	n/a	n/a
3	ATF2	chr12:20297229-20297703	GM12878	blood:	n/a	n/a
4	BATF	chr12:20340989-20341339	GM12878	blood:	n/a	chr12:20341161-20341172
5	BATF	chr12:20295925-20296216	GM12878	blood:	n/a	n/a
6	BCL11A	chr12:20297361-20297613	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:20293717-20294055	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:20297305-20297951	GM12878	blood:	n/a	n/a
9	CBX3	chr12:20347140-20347573	HCT-116	colon:	n/a	n/a
10	CEBPB	chr12:20278263-20278750	Hela-S3	cervix:	n/a	chr12:20278605-20278622 chr12:20278375-20278388 chr12:20278607-20278618
11	CEBPB	chr12:20280410-20280672	A549	lung:	n/a	chr12:20280555-20280568
12	CEBPB	chr12:20278521-20278717	A549	lung:	n/a	chr12:20278605-20278622 chr12:20278607-20278618
13	CEBPB	chr12:20341277-20341393	HepG2	liver:	n/a	chr12:20341331-20341342
14	CEBPB	chr12:20303749-20304367	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr12:20334187-20334599	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:20283016-20283081	HepG2	liver:	n/a	chr12:20283026-20283037
17	CEBPB	chr12:20280254-20280765	Hela-S3	cervix:	n/a	chr12:20280555-20280568
18	CEBPB	chr12:20278542-20278708	HepG2	liver:	n/a	chr12:20278605-20278622 chr12:20278607-20278618
19	CREB1	chr12:20297299-20297715	GM12878	blood:	n/a	chr12:20297535-20297548
20	CTCF	chr12:20284229-20284264	Lung_OC	lung:	n/a	n/a
21	CTCF	chr12:20347240-20347390	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr12:20296004-20296145	H1-hESC	embryonic stem cell:	n/a	chr12:20296045-20296063
23	CTCF	chr12:20347220-20347370	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr12:20347220-20347370	AG04449	skin:	n/a	n/a
25	CTCF	chr12:20347200-20347350	Caco-2	colon:	n/a	n/a
26	CTCF	chr12:20303780-20303930	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr12:20347158-20347406	GM12878	blood:	n/a	n/a
28	CTCF	chr12:20347242-20347371	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:20289540-20289690	GM12864	blood:	n/a	n/a
30	CTCF	chr12:20347226-20347395	LNCaP	prostate:	n/a	n/a
31	CTCF	chr12:20295915-20296210	H1-hESC	embryonic stem cell:	n/a	chr12:20296045-20296063
32	CTCF	chr12:20347226-20347348	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr12:20295980-20296130	HRPEpiC	eye:	n/a	chr12:20296045-20296063
34	CTCF	chr12:20296060-20296210	NHLF	lung:	n/a	n/a
35	CTCF	chr12:20347200-20347350	GM12865	blood:	n/a	n/a
36	CTCF	chr12:20347220-20347370	BJ	skin:	n/a	n/a
37	CTCF	chr12:20295960-20296110	GM12878	blood:	n/a	chr12:20296045-20296063
38	CTCF	chr12:20295720-20296010	HMF	breast:	n/a	n/a
39	CTCF	chr12:20347220-20347370	HAc	cerebellar:	n/a	n/a
40	CTCF	chr12:20296058-20296101	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:20296000-20296150	GM06990	blood:	n/a	chr12:20296045-20296063
42	CTCF	chr12:20347212-20347412	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:20347240-20347390	GM12865	blood:	n/a	n/a
44	CTCF	chr12:20347240-20347390	AG04450	lung:	n/a	n/a
45	CTCF	chr12:20347220-20347370	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr12:20347180-20347330	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr12:20295960-20296110	HCT-116	colon:	n/a	chr12:20296045-20296063
48	CTCF	chr12:20347260-20347410	HFF	foreskin:	n/a	n/a
49	CTCF	chr12:20295980-20296130	HCPEpiC	choroid plexus:	n/a	chr12:20296045-20296063
50	CTCF	chr12:20347200-20347350	SK-N-SH_RA	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:20336617-20336667	U87	brain:	n/a
2	chr12:20336617-20336667	MCF-7	breast:	n/a
3	chr12:20336617-20336667	K562	blood:	n/a
4	chr12:20336617-20336667	GM12891	blood:	n/a
5	chr12:20336617-20336667	HCM	heart:	n/a
6	chr12:20336617-20336667	RPTEC	kidney:	n/a
7	chr12:20336617-20336667	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:20336617-20336667	SK-N-SH	brain:	n/a
9	chr12:20336617-20336667	ECC-1	luminal epithelium:	n/a
10	chr12:20336617-20336667	PFSK-1	brain:	n/a
11	chr12:20336617-20336667	Hepatocyte	liver:	n/a
12	chr12:20336617-20336667	HepG2	liver:	n/a
13	chr12:20336617-20336667	NHDF-neo	bronchial:	n/a
14	chr12:20336617-20336667	IMR90	lung:	fetal
15	chr12:20336617-20336667	AG04450	lung:	fetal
16	chr12:20336617-20336667	H1-hESC	embryonic stem cell:	embryo
17	chr12:20336617-20336667	HRPEpiC	eye:	n/a
18	chr12:20336617-20336667	GM12878	blood:	n/a
19	chr12:20336617-20336667	AG04449	skin:	fetal
20	chr12:20336617-20336667	GM12892	blood:	n/a
21	chr12:20336617-20336667	SAEC	small airway:	n/a
22	chr12:20336617-20336667	GM06990	blood:	n/a
23	chr12:20336617-20336667	HEEpiC	esophagus:	n/a
24	chr12:20336617-20336667	HNPCEpiC	eye:	n/a
25	chr12:20336617-20336667	NT2-D1	testis:	n/a
26	chr12:20336617-20336667	GM19239	blood:	n/a
27	chr12:20336617-20336667	BJ	skin:	n/a
28	chr12:20336617-20336667	HRCEpiC	kidney:	n/a
29	chr12:20336617-20336667	LNCaP	prostate:	n/a
30	chr12:20336617-20336667	MCF10A-Er-Src	breast:	n/a
31	chr12:20336617-20336667	HMEC	breast:	n/a
32	chr12:20336617-20336667	Caco-2	colon:	n/a
33	chr12:20336617-20336667	HRE	kidney:	n/a
34	chr12:20336617-20336667	NHBE	bronchial:	n/a
35	chr12:20336617-20336667	AG10803	skin:	n/a
36	chr12:20336617-20336667	PANC-1	pancreas:	n/a
37	chr12:20336617-20336667	HAEpiC	amniotic membrane:	n/a
38	chr12:20336617-20336667	BE2_C	brain:	n/a
39	chr12:20336617-20336667	Hela-S3	cervix:	n/a
40	chr12:20336617-20336667	ovcar-3	ovarian:	n/a
41	chr12:20336617-20336667	T-47D	breast:	n/a
42	chr12:20336617-20336667	SK-N-SH_RA	brain:	n/a
43	chr12:20336617-20336667	PrEC	prostate:	n/a
44	chr12:20336617-20336667	HIPEpiC	eye:	n/a
45	chr12:20336617-20336667	HUVEC	blood vessel:	n/a
46	chr12:20336617-20336667	AoSMC	blood vessel:	n/a
47	chr12:20336617-20336667	Jurkat	blood:	n/a
48	chr12:20336617-20336667	HCPEpiC	choroid plexus:	n/a
49	chr12:20336617-20336667	HEK293	kidney:	embryo
50	chr12:20336617-20336667	A549	lung:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:20299715..20301403-chr21:38005000..38006593,2	MCF-7	breast:
2	chr12:20291329..20292956-chr12:20366236..20367919,2	K562	blood:
3	chr12:20305592..20306482-chr5:102206551..102207078,2	MCF-7	breast:
4	chr12:20225625..20228199-chr12:20277636..20280169,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1A2-3	chr12:20282589-20282795	XLOC_010027
2	lnc-SLCO1A2-3	chr12:20278673-20278769	ENSG00000256499
3	lnc-SLCO1A2-3	chr12:20278745-20278769	XLOC_010027
4	lnc-SLCO1A2-3	chr12:20280750-20280892	ENSG00000256499
5	lnc-SLCO1A2-3	chr12:20282589-20282747	ENSG00000256499
6	lnc-SLCO1A2-3	chr12:20280750-20280888	XLOC_010027

No data

Variant related genes	Relation type
ENSG00000256499	TF binding region
ENSG00000256499	CpG island
SERBP1	miRNA target sites
MAPK11	miRNA target sites
MAPK14	miRNA target sites
FNDC3B	miRNA target sites
MAPK1	miRNA target sites
CEP63	miRNA target sites

Extended variants
information (count: 3049 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3049 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2303658	chr12:20278430-20278431	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190524055	chr12:20278431-20278432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532975787	chr12:20278446-20278447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543075884	chr12:20278485-20278486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181287126	chr12:20278535-20278536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150976969	chr12:20278551-20278552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549054167	chr12:20278605-20278606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566325729	chr12:20278672-20278673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185538963	chr12:20278680-20278681	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs191141529	chr12:20278682-20278683	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs563565842	chr12:20278760-20278761	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs370905576	chr12:20278839-20278840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7299269	chr12:20278886-20278887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79286143	chr12:20278893-20278894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376008946	chr12:20278952-20278953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145857947	chr12:20278973-20278974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115857043	chr12:20279002-20279003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549457431	chr12:20279017-20279018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567608984	chr12:20279030-20279031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536348626	chr12:20279051-20279052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368814210	chr12:20279054-20279055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571949261	chr12:20279055-20279056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138689177	chr12:20279199-20279200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372176760	chr12:20279209-20279210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566253398	chr12:20279257-20279258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12308800	chr12:20279287-20279288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11609944	chr12:20279290-20279291	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182964338	chr12:20279309-20279310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563143163	chr12:20279318-20279319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528879996	chr12:20279336-20279337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542786076	chr12:20279349-20279350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113891529	chr12:20279376-20279377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146918134	chr12:20279400-20279401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552025502	chr12:20279412-20279413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571778627	chr12:20279455-20279456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531119824	chr12:20279488-20279489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75464280	chr12:20279495-20279496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs17373317	chr12:20279517-20279518	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs187552315	chr12:20279535-20279536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536235111	chr12:20279544-20279545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76280554	chr12:20279549-20279550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536786325	chr12:20279602-20279603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566601957	chr12:20279636-20279637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75285518	chr12:20279640-20279641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149631229	chr12:20279652-20279653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577721715	chr12:20279660-20279661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372894138	chr12:20279710-20279711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543401080	chr12:20279741-20279742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs67437207	chr12:20279769-20279770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557213252	chr12:20279775-20279776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20258800-20327400	Weak transcription	Aorta	Aorta
2	chr12:20268600-20289200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:20278000-20279000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:20278000-20279000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:20278000-20281200	Enhancers	Hela-S3	cervix
6	chr12:20278200-20278600	Enhancers	Brain Germinal Matrix	brain
7	chr12:20278200-20278800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr12:20278200-20279000	Enhancers	Colon Smooth Muscle	Colon
9	chr12:20278200-20279800	Enhancers	Rectal Smooth Muscle	rectum
10	chr12:20278800-20280200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr12:20279000-20279400	Weak transcription	Colon Smooth Muscle	Colon
12	chr12:20279000-20280200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:20279400-20280600	Enhancers	Colon Smooth Muscle	Colon
14	chr12:20279800-20289000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr12:20280200-20280400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:20280200-20281000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr12:20280600-20281000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr12:20280600-20281000	Enhancers	NHDF-Ad	bronchial
19	chr12:20280600-20295000	Weak transcription	Colon Smooth Muscle	Colon
20	chr12:20280800-20281000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:20281200-20281600	Weak transcription	Hela-S3	cervix
22	chr12:20281600-20282200	Enhancers	Hela-S3	cervix
23	chr12:20282200-20285800	Weak transcription	Hela-S3	cervix
24	chr12:20285800-20286000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:20285800-20286200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:20285800-20286200	Enhancers	Hela-S3	cervix
27	chr12:20286000-20286400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr12:20286000-20288800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:20288200-20288600	Enhancers	Fetal Muscle Trunk	muscle
30	chr12:20288800-20289800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr12:20289200-20289800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr12:20289400-20289800	Enhancers	Fetal Heart	heart
33	chr12:20293800-20294400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr12:20295000-20295600	Enhancers	Fetal Stomach	stomach
35	chr12:20295000-20296000	Enhancers	Colon Smooth Muscle	Colon
36	chr12:20295000-20296200	Enhancers	Rectal Smooth Muscle	rectum
37	chr12:20295200-20296000	Enhancers	Fetal Lung	lung
38	chr12:20295200-20296200	Enhancers	Stomach Smooth Muscle	stomach
39	chr12:20295200-20296400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr12:20296600-20297400	Enhancers	GM12878-XiMat	blood
41	chr12:20303400-20304400	Enhancers	HUVEC	blood vessel
42	chr12:20303600-20304000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr12:20303600-20304200	Enhancers	Fetal Intestine Small	intestine
44	chr12:20303600-20304400	Enhancers	Fetal Kidney	kidney
45	chr12:20303800-20304200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:20303800-20304400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr12:20303800-20304400	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr12:20304000-20304400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr12:20304200-20307200	Weak transcription	Fetal Intestine Small	intestine
50	chr12:20306800-20308800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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