Variant report

Variant	nsv525100
Chromosome Location	chr12:29576517-29585955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:329)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:29581667-29581980	K562	blood:	n/a	n/a
2	ATF2	chr12:29581583-29582056	GM12878	blood:	n/a	n/a
3	ATF3	chr12:29581552-29582134	HCT-116	colon:	n/a	n/a
4	BATF	chr12:29581664-29581970	GM12878	blood:	n/a	chr12:29581803-29581814
5	BCL3	chr12:29581711-29581989	GM12878	blood:	n/a	chr12:29581807-29581816
6	BDP1	chr12:29581674-29582096	Hela-S3	cervix:	n/a	n/a
7	BHLHE40	chr12:29580984-29581302	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:29580970-29581287	K562	blood:	n/a	n/a
9	BRCA1	chr12:29583383-29583533	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr12:29581479-29582146	HCT-116	colon:	n/a	n/a
11	CEBPB	chr12:29581616-29581936	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:29581577-29581987	IMR90	lung:	n/a	n/a
13	CEBPB	chr12:29581048-29582065	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:29581379-29582148	HCT-116	colon:	n/a	n/a
15	CEBPB	chr12:29581581-29582039	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr12:29581449-29582118	HCT-116	colon:	n/a	n/a
17	CEBPB	chr12:29581591-29581924	K562	blood:	n/a	n/a
18	CEBPB	chr12:29581592-29581925	K562	blood:	n/a	n/a
19	CEBPB	chr12:29582868-29583697	Hela-S3	cervix:	n/a	chr12:29582868-29582880
20	CEBPB	chr12:29581604-29582117	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr12:29581659-29581848	K562	blood:	n/a	n/a
22	CHD1	chr12:29581054-29581200	GM12878	blood:	n/a	n/a
23	CHD2	chr12:29580921-29581414	GM12878	blood:	n/a	n/a
24	CHD2	chr12:29581533-29582044	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr12:29583235-29583652	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr12:29581040-29581190	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr12:29581045-29581173	HepG2	liver:	n/a	n/a
28	CTCF	chr12:29581120-29581270	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr12:29580995-29581053	GM12892	blood:	n/a	n/a
30	CTCF	chr12:29581060-29581210	GM12868	blood:	n/a	n/a
31	CTCF	chr12:29581020-29581170	HEK293	kidney:	n/a	n/a
32	CTCF	chr12:29581040-29581190	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr12:29581000-29581150	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr12:29581040-29581190	GM12870	blood:	n/a	n/a
35	CTCF	chr12:29580813-29581327	K562	blood:	n/a	n/a
36	CTCF	chr12:29580978-29581121	GM19240	blood:	n/a	n/a
37	CTCF	chr12:29580915-29581252	K562	blood:	n/a	n/a
38	CTCF	chr12:29581020-29581170	GM12871	blood:	n/a	n/a
39	CTCF	chr12:29580436-29580491	GM10266	blood:	n/a	n/a
40	CTCF	chr12:29581100-29581250	RPTEC	kidney:	n/a	n/a
41	CTCF	chr12:29581060-29581210	GM12864	blood:	n/a	n/a
42	CTCF	chr12:29580917-29581314	GM12878	blood:	n/a	n/a
43	CTCF	chr12:29580994-29581272	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:29580991-29581230	K562	blood:	n/a	n/a
45	CTCF	chr12:29581000-29581150	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr12:29580986-29581245	GM12878	blood:	n/a	n/a
47	CTCF	chr12:29581000-29581150	GM12873	blood:	n/a	n/a
48	CTCF	chr12:29581040-29581190	BE2_C	brain:	n/a	n/a
49	CTCF	chr12:29580933-29581268	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:29581020-29581170	HMEC	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:29581042-29581092	IMR90	lung:	fetal
2	chr12:29581042-29581092	HL-60	blood:	n/a
3	chr12:29581042-29581092	GM19239	blood:	n/a
4	chr12:29581042-29581092	AoSMC	blood vessel:	n/a
5	chr12:29581042-29581092	SK-N-SH	brain:	n/a
6	chr12:29581042-29581092	Jurkat	blood:	n/a
7	chr12:29581042-29581092	HCF	heart:	n/a
8	chr12:29581042-29581092	LNCaP	prostate:	n/a
9	chr12:29581042-29581092	PFSK-1	brain:	n/a
10	chr12:29581042-29581092	GM12891	blood:	n/a
11	chr12:29581042-29581092	GM06990	blood:	n/a
12	chr12:29581042-29581092	HCM	heart:	n/a
13	chr12:29581042-29581092	SAEC	small airway:	n/a
14	chr12:29581042-29581092	GM12878	blood:	n/a
15	chr12:29581042-29581092	HRCEpiC	kidney:	n/a
16	chr12:29581042-29581092	HCT-116	colon:	n/a
17	chr12:29581042-29581092	MCF-7	breast:	n/a
18	chr12:29581042-29581092	ECC-1	luminal epithelium:	n/a
19	chr12:29581042-29581092	ProgFib	skin:	n/a
20	chr12:29581042-29581092	HMEC	breast:	n/a
21	chr12:29581042-29581092	HUVEC	blood vessel:	n/a
22	chr12:29581042-29581092	NT2-D1	testis:	n/a
23	chr12:29581042-29581092	MCF10A-Er-Src	breast:	n/a
24	chr12:29581042-29581092	ovcar-3	ovarian:	n/a
25	chr12:29581042-29581092	Hela-S3	cervix:	n/a
26	chr12:29581042-29581092	HIPEpiC	eye:	n/a
27	chr12:29581042-29581092	HCPEpiC	choroid plexus:	n/a
28	chr12:29581042-29581092	NHBE	bronchial:	n/a
29	chr12:29581042-29581092	HEK293	kidney:	embryo
30	chr12:29581042-29581092	HepG2	liver:	n/a
31	chr12:29581042-29581092	HAEpiC	amniotic membrane:	n/a
32	chr12:29581042-29581092	BJ	skin:	n/a
33	chr12:29581042-29581092	SK-N-SH_RA	brain:	n/a
34	chr12:29581042-29581092	AG09309	skin:	n/a
35	chr12:29581042-29581092	RPTEC	kidney:	n/a
36	chr12:29581042-29581092	BE2_C	brain:	n/a
37	chr12:29581042-29581092	Caco-2	colon:	n/a
38	chr12:29581042-29581092	HPAEpiC	pulmonary alveolar:	n/a
39	chr12:29581042-29581092	K562	blood:	n/a
40	chr12:29581042-29581092	NH-A	brain:	n/a
41	chr12:29581042-29581092	U87	brain:	n/a
42	chr12:29581042-29581092	HRE	kidney:	n/a
43	chr12:29581042-29581092	PANC-1	pancreas:	n/a
44	chr12:29581042-29581092	AG09319	gingival:	n/a
45	chr12:29581042-29581092	HRPEpiC	eye:	n/a
46	chr12:29581042-29581092	SKMC	muscle:	n/a
47	chr12:29581042-29581092	AG04450	lung:	fetal
48	chr12:29581042-29581092	A549	lung:	n/a
49	chr12:29581042-29581092	NHDF-neo	bronchial:	n/a
50	chr12:29581042-29581092	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr12:29540594..29543484-chr12:29574878..29577697,2	K562	blood:
2	chr12:29570616..29572170-chr12:29576481..29578038,2	K562	blood:
3	chr12:29581032..29583088-chr12:29583675..29586348,2	K562	blood:
4	chr12:29581032..29583088-chr12:29583675..29586348,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-677C1.2.1-2	chr12:29578858-29578997	NONHSAT027492

No data

Variant related genes	Relation type
OVCH1-AS1	TF binding region
OVCH1-AS1	CpG island
ENSG00000257599	chromatin interactions

Extended variants
information (count: 315 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2042512	chr12:29576517-29576518	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75157149	chr12:29576521-29576522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558729321	chr12:29576534-29576535	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs570803878	chr12:29576558-29576559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182653471	chr12:29576623-29576624	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs187077008	chr12:29576679-29576680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192623462	chr12:29576683-29576684	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568950008	chr12:29576696-29576697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs77473561	chr12:29576699-29576700	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145219546	chr12:29576706-29576707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149135371	chr12:29576723-29576724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs575040167	chr12:29576747-29576748	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559440246	chr12:29576755-29576756	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs563958311	chr12:29576757-29576758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs145180173	chr12:29576759-29576760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78000857	chr12:29576784-29576785	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577717631	chr12:29576900-29576901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs371592754	chr12:29576901-29576902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562021617	chr12:29576911-29576912	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529161641	chr12:29576912-29576913	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140700944	chr12:29576916-29576917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs562669342	chr12:29576921-29576922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557530268	chr12:29576938-29576939	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs374505888	chr12:29576985-29576986	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531056461	chr12:29576999-29577000	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552654771	chr12:29577046-29577047	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570829317	chr12:29577079-29577080	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535020290	chr12:29577085-29577086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546636486	chr12:29577144-29577145	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs11050227	chr12:29577199-29577200	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs184371483	chr12:29577214-29577215	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs148130126	chr12:29577227-29577228	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs7954043	chr12:29577238-29577239	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs561500068	chr12:29577274-29577275	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11050228	chr12:29577368-29577369	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs532031949	chr12:29577383-29577384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557858391	chr12:29577423-29577424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12831249	chr12:29577470-29577471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs540234489	chr12:29577484-29577485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544601231	chr12:29577502-29577503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs150113986	chr12:29577526-29577527	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138412154	chr12:29577587-29577588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs73276831	chr12:29577620-29577621	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs562707985	chr12:29577663-29577664	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs77506230	chr12:29577664-29577665	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs551241086	chr12:29577678-29577679	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs73276833	chr12:29577707-29577708	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs528567062	chr12:29577740-29577741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs193145433	chr12:29577742-29577743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10219521	chr12:29577767-29577768	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

Disease	PMID	Source
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
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	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 myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	17133270	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29571000-29583400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:29578000-29583200	Enhancers	Hela-S3	cervix
3	chr12:29578200-29580000	Enhancers	HUVEC	blood vessel
4	chr12:29578400-29579000	Enhancers	HMEC	breast
5	chr12:29578400-29579200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:29578400-29579200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr12:29578400-29579400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr12:29578600-29579000	Enhancers	NHEK	skin
9	chr12:29578600-29579600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:29579000-29581200	Weak transcription	HMEC	breast
11	chr12:29579000-29581400	Weak transcription	NHEK	skin
12	chr12:29579200-29581200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr12:29579400-29581200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr12:29579600-29581400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:29579800-29580800	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr12:29579800-29583800	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr12:29580000-29581400	Weak transcription	HUVEC	blood vessel
18	chr12:29580000-29583400	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr12:29580400-29581200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr12:29580400-29582000	Enhancers	GM12878-XiMat	blood
21	chr12:29580800-29581400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:29580800-29581600	Enhancers	K562	blood
23	chr12:29580800-29581800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:29580800-29582200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr12:29581200-29581600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr12:29581200-29581600	Enhancers	HSMMtube	muscle
27	chr12:29581200-29581800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr12:29581200-29581800	Enhancers	Muscle Satellite Cultured Cells	--
29	chr12:29581200-29582400	Enhancers	HMEC	breast
30	chr12:29581200-29583800	Enhancers	Duodenum Mucosa	Duodenum
31	chr12:29581400-29581800	Enhancers	HUVEC	blood vessel
32	chr12:29581400-29582000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr12:29581400-29582400	Enhancers	NHEK	skin
34	chr12:29581400-29582600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:29581400-29584000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:29581600-29581800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:29581600-29581800	Enhancers	Liver	Liver
38	chr12:29581600-29583200	Weak transcription	K562	blood
39	chr12:29581600-29604200	Weak transcription	HSMMtube	muscle
40	chr12:29581800-29583000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:29581800-29613600	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr12:29582200-29583600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr12:29582400-29582800	Weak transcription	HMEC	breast
44	chr12:29582400-29582800	Weak transcription	NHEK	skin
45	chr12:29582600-29583000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:29582800-29583200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:29582800-29583400	Weak transcription	Liver	Liver
48	chr12:29582800-29583800	Enhancers	NHEK	skin
49	chr12:29582800-29584000	Enhancers	HMEC	breast
50	chr12:29583000-29583800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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