Variant report

Variant	nsv560499
Chromosome Location	chr12:124389150-124396816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:245)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124395591-124395654	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:124389898-124390096	HepG2	liver:	n/a	chr12:124389984-124389995
3	CEBPB	chr12:124389848-124390167	ECC-1	luminal epithelium:	n/a	chr12:124389984-124389995
4	CEBPB	chr12:124389783-124390267	MCF-7	breast:	n/a	chr12:124389984-124389995
5	CEBPB	chr12:124389816-124390173	A549	lung:	n/a	chr12:124389984-124389995
6	CEBPB	chr12:124389804-124390174	K562	blood:	n/a	chr12:124389984-124389995
7	CEBPB	chr12:124389816-124390178	H1-hESC	embryonic stem cell:	n/a	chr12:124389984-124389995
8	CEBPB	chr12:124389682-124390301	A549	lung:	n/a	chr12:124389984-124389995
9	CEBPB	chr12:124389821-124390187	HepG2	liver:	n/a	chr12:124389984-124389995
10	CEBPB	chr12:124392389-124392460	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:124389793-124390177	IMR90	lung:	n/a	chr12:124389984-124389995
12	CEBPB	chr12:124389800-124390188	Hela-S3	cervix:	n/a	chr12:124389984-124389995
13	CEBPB	chr12:124389751-124390130	MCF-7	breast:	n/a	chr12:124389984-124389995
14	CHD2	chr12:124395411-124395440	HepG2	liver:	n/a	n/a
15	CTCF	chr12:124389702-124389829	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr12:124389977-124390112	MCF-7	breast:	n/a	n/a
17	CTCF	chr12:124389839-124390241	A549	lung:	n/a	n/a
18	CTCF	chr12:124390020-124390170	AG09309	skin:	n/a	n/a
19	CTCF	chr12:124390020-124390170	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr12:124390020-124390170	RPTEC	kidney:	n/a	n/a
21	CTCF	chr12:124389935-124390219	GM12878	blood:	n/a	n/a
22	CTCF	chr12:124389948-124390149	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr12:124389980-124390130	AG04449	skin:	n/a	n/a
24	CTCF	chr12:124390000-124390150	GM12866	blood:	n/a	n/a
25	CTCF	chr12:124389620-124389770	HCM	heart:	n/a	n/a
26	CTCF	chr12:124389836-124390280	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr12:124390020-124390170	GM12867	blood:	n/a	n/a
28	CTCF	chr12:124389960-124390110	HEK293	kidney:	n/a	n/a
29	CTCF	chr12:124390000-124390150	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr12:124390000-124390150	AG09319	gingival:	n/a	n/a
31	CTCF	chr12:124389980-124390130	NHEK	skin:	n/a	n/a
32	CTCF	chr12:124389784-124389786	GM10248	blood:	n/a	n/a
33	CTCF	chr12:124390000-124390150	HAc	cerebellar:	n/a	n/a
34	CTCF	chr12:124389863-124390275	GM12878	blood:	n/a	n/a
35	CTCF	chr12:124389940-124390090	HMEC	breast:	n/a	n/a
36	CTCF	chr12:124390020-124390170	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr12:124389824-124390402	HCT-116	colon:	n/a	n/a
38	CTCF	chr12:124389980-124390130	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr12:124389961-124390238	ECC-1	luminal epithelium:	n/a	n/a
40	CTCF	chr12:124389960-124390110	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr12:124389960-124390110	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr12:124389940-124390090	GM12875	blood:	n/a	n/a
43	CTCF	chr12:124389960-124390110	GM12867	blood:	n/a	n/a
44	CTCF	chr12:124389977-124390192	HepG2	liver:	n/a	n/a
45	CTCF	chr12:124390020-124390170	HEK293	kidney:	n/a	n/a
46	CTCF	chr12:124389932-124390193	LNCaP	prostate:	n/a	n/a
47	CTCF	chr12:124389954-124390182	GM20000	blood:	n/a	n/a
48	CTCF	chr12:124389928-124390226	Medullo	brain:	n/a	n/a
49	CTCF	chr12:124390000-124390150	AG04450	lung:	n/a	n/a
50	CTCF	chr12:124389990-124390083	H1-hESC	embryonic stem cell:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124393772-124393822	GM12892	blood:	n/a
2	chr12:124393772-124393822	GM12892	blood:	n/a
3	chr12:124392362-124392412	MCF-7	breast:	n/a
4	chr12:124393913-124393963	NHDF-neo	bronchial:	n/a
5	chr12:124393655-124393705	GM19239	blood:	n/a
6	chr12:124393772-124393822	HUVEC	blood vessel:	n/a
7	chr12:124393913-124393963	HepG2	liver:	n/a
8	chr12:124392362-124392412	GM19239	blood:	n/a
9	chr12:124393655-124393705	IMR90	lung:	fetal
10	chr12:124392362-124392412	HCPEpiC	choroid plexus:	n/a
11	chr12:124392362-124392412	SK-N-SH	brain:	n/a
12	chr12:124393772-124393822	GM12878	blood:	n/a
13	chr12:124392362-124392412	HMEC	breast:	n/a
14	chr12:124392362-124392412	LNCaP	prostate:	n/a
15	chr12:124393655-124393705	AG04449	skin:	fetal
16	chr12:124393913-124393963	MCF10A-Er-Src	breast:	n/a
17	chr12:124393913-124393963	Hepatocyte	liver:	n/a
18	chr12:124392362-124392412	T-47D	breast:	n/a
19	chr12:124393913-124393963	Jurkat	blood:	n/a
20	chr12:124393655-124393705	Hepatocyte	liver:	n/a
21	chr12:124393913-124393963	SKMC	muscle:	n/a
22	chr12:124393913-124393963	SK-N-SH	brain:	n/a
23	chr12:124393913-124393963	GM19239	blood:	n/a
24	chr12:124393655-124393705	HAEpiC	amniotic membrane:	n/a
25	chr12:124392362-124392412	RPTEC	kidney:	n/a
26	chr12:124393772-124393822	H1-hESC	embryonic stem cell:	embryo
27	chr12:124393655-124393705	PFSK-1	brain:	n/a
28	chr12:124393913-124393963	HL-60	blood:	n/a
29	chr12:124393913-124393963	HRCEpiC	kidney:	n/a
30	chr12:124393913-124393963	BE2_C	brain:	n/a
31	chr12:124393913-124393963	GM12891	blood:	n/a
32	chr12:124393772-124393822	AG04450	lung:	fetal
33	chr12:124393772-124393822	HIPEpiC	eye:	n/a
34	chr12:124393913-124393963	CMK	blood:	n/a
35	chr12:124393913-124393963	BJ	skin:	n/a
36	chr12:124393772-124393822	Caco-2	colon:	n/a
37	chr12:124393772-124393822	GM06990	blood:	n/a
38	chr12:124393655-124393705	HRPEpiC	eye:	n/a
39	chr12:124393772-124393822	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:124393913-124393963	NHBE	bronchial:	n/a
41	chr12:124392362-124392412	HUVEC	blood vessel:	n/a
42	chr12:124393772-124393822	AoSMC	blood vessel:	n/a
43	chr12:124392362-124392412	IMR90	lung:	fetal
44	chr12:124392362-124392412	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:124393913-124393963	IMR90	lung:	fetal
46	chr12:124393913-124393963	NH-A	brain:	n/a
47	chr12:124392362-124392412	Hepatocyte	liver:	n/a
48	chr12:124393772-124393822	SK-N-SH	brain:	n/a
49	chr12:124393913-124393963	AG04449	skin:	fetal
50	chr12:124393913-124393963	AG09319	gingival:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:124389629..124391597-chr12:124394347..124396284,2	K562	blood:
2	chr12:124380887..124382932-chr12:124386966..124389727,2	K562	blood:
3	chr12:124389629..124391597-chr12:124394347..124396284,2	K562	blood:
4	chr12:124387569..124390026-chr12:124455814..124457883,2	MCF-7	breast:
5	chr12:124295197..124298095-chr12:124388889..124391568,2	MCF-7	breast:
6	chr12:124389950..124393053-chr12:124455413..124457949,3	MCF-7	breast:
7	chr1:109583884..109584598-chr12:124392910..124393430,2	Hela-S3	cervix:
8	chr12:124369425..124371891-chr12:124388110..124389965,2	MCF-7	breast:
9	chr12:124389600..124390517-chr12:124516534..124517510,2	K562	blood:

No data

Variant related genes	Relation type
DNAH10	TF binding region
DNAH10	CpG island
ENSG00000270095	chromatin interactions
ENSG00000085433	chromatin interactions
ENSG00000119242	chromatin interactions
ENSG00000178882	chromatin interactions
ENSG00000179195	chromatin interactions

Extended variants
information (count: 346 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:346 , 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	rs12309481	chr12:124389150-124389151	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553230134	chr12:124389167-124389168	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs111797153	chr12:124389187-124389188	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs61464740	chr12:124389278-124389279	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs538609498	chr12:124389300-124389301	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs181705640	chr12:124389339-124389340	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs575897187	chr12:124389360-124389361	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs186782802	chr12:124389403-124389404	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs561526495	chr12:124389415-124389416	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs570885151	chr12:124389435-124389436	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs373274303	chr12:124389436-124389437	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs573549273	chr12:124389523-124389524	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs35322017	chr12:124389542-124389543	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs34678811	chr12:124389633-124389634	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs367877081	chr12:124389692-124389693	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs541113152	chr12:124389695-124389696	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs559135867	chr12:124389716-124389717	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs533067884	chr12:124389723-124389724	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs551053235	chr12:124389767-124389768	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs563304734	chr12:124389771-124389772	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs150245611	chr12:124389780-124389781	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs531208216	chr12:124389783-124389784	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs77742416	chr12:124389821-124389822	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs550173134	chr12:124389859-124389860	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs137939447	chr12:124389881-124389882	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs570084104	chr12:124389883-124389884	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs142519842	chr12:124389886-124389887	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs556007210	chr12:124389937-124389938	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs547176649	chr12:124389975-124389976	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs572687407	chr12:124389985-124389986	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs571623426	chr12:124389990-124389991	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs35835989	chr12:124389995-124389996	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs116558952	chr12:124389999-124390000	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs556921486	chr12:124390000-124390001	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs568941413	chr12:124390043-124390044	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs536947134	chr12:124390142-124390143	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs79348271	chr12:124390186-124390187	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs192238120	chr12:124390265-124390266	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs183438591	chr12:124390345-124390346	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs555284401	chr12:124390360-124390361	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs144081178	chr12:124390378-124390379	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs113767728	chr12:124390447-124390448	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs184985510	chr12:124390457-124390458	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs532280211	chr12:124390527-124390528	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs189844977	chr12:124390528-124390529	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs563268821	chr12:124390563-124390564	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs112703259	chr12:124390589-124390590	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs182250193	chr12:124390607-124390608	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs148272529	chr12:124390633-124390634	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs528803863	chr12:124390650-124390651	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124382000-124391400	Weak transcription	Fetal Lung	lung
2	chr12:124384000-124408400	Weak transcription	Fetal Brain Female	brain
3	chr12:124385400-124390200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr12:124386000-124391400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:124386000-124395800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:124386200-124390800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:124386200-124392000	Weak transcription	NH-A	brain
8	chr12:124386200-124392200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:124386200-124394000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:124386800-124391800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:124387200-124392000	Weak transcription	Fetal Thymus	thymus
12	chr12:124388400-124391800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr12:124388800-124389600	Enhancers	Fetal Kidney	kidney
14	chr12:124389600-124389800	Enhancers	Brain Hippocampus Middle	brain
15	chr12:124389600-124390000	Weak transcription	Fetal Kidney	kidney
16	chr12:124389600-124390400	Enhancers	Fetal Intestine Small	intestine
17	chr12:124389800-124390000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr12:124389800-124390000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr12:124389800-124390000	Enhancers	HMEC	breast
20	chr12:124389800-124390400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr12:124389800-124390400	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr12:124389800-124390400	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr12:124389800-124390400	Enhancers	Brain Cingulate Gyrus	brain
24	chr12:124389800-124390400	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr12:124389800-124390400	Enhancers	NHDF-Ad	bronchial
26	chr12:124390000-124390200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:124390000-124390200	Enhancers	Fetal Kidney	kidney
28	chr12:124390000-124390600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr12:124390000-124392200	Weak transcription	Brain Hippocampus Middle	brain
30	chr12:124390200-124390400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:124390200-124391400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:124390200-124391600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr12:124390200-124391600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr12:124390200-124391800	Weak transcription	Fetal Kidney	kidney
35	chr12:124390200-124391800	Weak transcription	HMEC	breast
36	chr12:124390200-124397600	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr12:124390400-124390600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:124390400-124391600	Weak transcription	NHDF-Ad	bronchial
39	chr12:124390400-124392000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr12:124390400-124392000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr12:124390400-124392000	Weak transcription	Fetal Intestine Small	intestine
42	chr12:124390400-124392400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:124390600-124391800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:124390800-124392200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr12:124390800-124394400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr12:124391400-124392200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr12:124391400-124392600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:124391400-124392800	Enhancers	Fetal Lung	lung
49	chr12:124391400-124393000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr12:124391400-124393000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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