Variant report

Variant	nsv8884
Chromosome Location	chr12:523725-538589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:305)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:529788-530091	GM12878	blood:	n/a	n/a
2	BATF	chr12:529122-529352	GM12878	blood:	n/a	n/a
3	CEBPB	chr12:531506-531586	A549	lung:	n/a	chr12:531509-531520
4	CEBPB	chr12:531464-531635	HepG2	liver:	n/a	chr12:531509-531520
5	CTCF	chr12:526161-526202	GM13976	blood:	n/a	n/a
6	CTCF	chr12:529316-529351	GM10248	blood:	n/a	n/a
7	CTCF	chr12:533312-533395	Lung_OC	lung:	n/a	n/a
8	EP300	chr12:524035-524378	SK-N-SH_RA	brain:	n/a	n/a
9	EP300	chr12:530501-530637	GM12878	blood:	n/a	n/a
10	EP300	chr12:524029-524350	SK-N-SH_RA	brain:	n/a	n/a
11	FOXA2	chr12:532511-532883	A549	lung:	n/a	n/a
12	GABPA	chr12:529122-529608	Hela-S3	cervix:	n/a	n/a
13	GABPA	chr12:530914-531300	Hela-S3	cervix:	n/a	n/a
14	GABPA	chr12:530322-530843	Hela-S3	cervix:	n/a	n/a
15	GABPA	chr12:529788-530251	Hela-S3	cervix:	n/a	n/a
16	GATA2	chr12:529782-530119	K562	blood:	n/a	n/a
17	GATA2	chr12:529143-529427	K562	blood:	n/a	n/a
18	HEY1	chr12:529791-530300	K562	blood:	n/a	n/a
19	IRF4	chr12:529086-529477	GM12878	blood:	n/a	n/a
20	IRF4	chr12:530317-530809	GM12878	blood:	n/a	n/a
21	IRF4	chr12:529752-530228	GM12878	blood:	n/a	n/a
22	MAFK	chr12:527580-527775	HepG2	liver:	n/a	n/a
23	MYC	chr12:523948-524469	A549	lung:	n/a	n/a
24	MYC	chr12:529381-529480	H1-hESC	embryonic stem cell:	n/a	n/a
25	PAX5	chr12:530910-531312	GM12878	blood:	n/a	n/a
26	PAX5	chr12:529742-530262	GM12878	blood:	n/a	n/a
27	PAX5	chr12:529076-529666	GM12878	blood:	n/a	n/a
28	PAX5	chr12:529866-530038	GM12878	blood:	n/a	n/a
29	PAX5	chr12:530318-530737	GM12878	blood:	n/a	n/a
30	PAX5	chr12:529200-529515	GM12878	blood:	n/a	n/a
31	PBX3	chr12:529158-529299	GM12878	blood:	n/a	n/a
32	PBX3	chr12:530586-530711	GM12878	blood:	n/a	n/a
33	PBX3	chr12:529824-530119	GM12878	blood:	n/a	n/a
34	POLR2A	chr12:534548-534559	GM12878	blood:	n/a	n/a
35	POLR2A	chr12:536082-536140	HepG2	liver:	n/a	n/a
36	POLR2A	chr12:529801-530393	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr12:530412-530459	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr12:529008-531486	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:529083-531443	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr12:534568-534651	GM12878	blood:	n/a	n/a
41	POLR2A	chr12:529229-529587	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr12:526898-527082	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr12:530946-531054	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr12:529129-529603	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr12:529135-529679	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr12:529795-531440	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr12:527880-528147	HepG2	liver:	n/a	n/a
48	POLR2A	chr12:529083-531462	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr12:529813-531417	GM12878	blood:	n/a	n/a
50	POLR2A	chr12:528519-528931	H1-hESC	embryonic stem cell:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:534669-534719	BE2_C	brain:	n/a
2	chr12:534669-534719	GM12878	blood:	n/a
3	chr12:534917-534967	T-47D	breast:	n/a
4	chr12:534753-534803	GM12878	blood:	n/a
5	chr12:534669-534719	NHDF-neo	bronchial:	n/a
6	chr12:534753-534803	HepG2	liver:	n/a
7	chr12:535855-535905	NH-A	brain:	n/a
8	chr12:535855-535905	PrEC	prostate:	n/a
9	chr12:534669-534719	HCT-116	colon:	n/a
10	chr12:534563-534613	SK-N-MC	brain:	n/a
11	chr12:534917-534967	HCT-116	colon:	n/a
12	chr12:534563-534613	RPTEC	kidney:	n/a
13	chr12:535855-535905	ProgFib	skin:	n/a
14	chr12:534563-534613	NHDF-neo	bronchial:	n/a
15	chr12:534669-534719	HRCEpiC	kidney:	n/a
16	chr12:534917-534967	BJ	skin:	n/a
17	chr12:534563-534613	HUVEC	blood vessel:	n/a
18	chr12:534669-534719	GM12892	blood:	n/a
19	chr12:535855-535905	HUVEC	blood vessel:	n/a
20	chr12:534563-534613	HCPEpiC	choroid plexus:	n/a
21	chr12:535855-535905	MCF-7	breast:	n/a
22	chr12:534669-534719	SAEC	small airway:	n/a
23	chr12:534753-534803	Hela-S3	cervix:	n/a
24	chr12:534753-534803	GM19239	blood:	n/a
25	chr12:534917-534967	SAEC	small airway:	n/a
26	chr12:534917-534967	AG04449	skin:	fetal
27	chr12:534753-534803	CMK	blood:	n/a
28	chr12:534563-534613	T-47D	breast:	n/a
29	chr12:534563-534613	K562	blood:	n/a
30	chr12:534753-534803	HCF	heart:	n/a
31	chr12:534917-534967	NHBE	bronchial:	n/a
32	chr12:535855-535905	GM19239	blood:	n/a
33	chr12:534917-534967	PFSK-1	brain:	n/a
34	chr12:534669-534719	Jurkat	blood:	n/a
35	chr12:534917-534967	ECC-1	luminal epithelium:	n/a
36	chr12:534753-534803	ECC-1	luminal epithelium:	n/a
37	chr12:534563-534613	Hela-S3	cervix:	n/a
38	chr12:534753-534803	HEK293	kidney:	embryo
39	chr12:534917-534967	HAEpiC	amniotic membrane:	n/a
40	chr12:535855-535905	SKMC	muscle:	n/a
41	chr12:534917-534967	NHDF-neo	bronchial:	n/a
42	chr12:534753-534803	HUVEC	blood vessel:	n/a
43	chr12:534669-534719	HRPEpiC	eye:	n/a
44	chr12:534917-534967	AG04450	lung:	fetal
45	chr12:534753-534803	SK-N-MC	brain:	n/a
46	chr12:534753-534803	LNCaP	prostate:	n/a
47	chr12:534563-534613	SAEC	small airway:	n/a
48	chr12:534753-534803	PrEC	prostate:	n/a
49	chr12:535855-535905	HNPCEpiC	eye:	n/a
50	chr12:534669-534719	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:510128..512811-chr12:522624..524245,2	MCF-7	breast:

No data

Variant related genes	Relation type
CCDC77	TF binding region
CCDC77	CpG island
ENSG00000120647	chromatin interactions

Extended variants
information (count: 852 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140032237	chr12:523732-523733	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552977221	chr12:523744-523745	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568269155	chr12:523748-523749	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116384151	chr12:523750-523751	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs149851424	chr12:523777-523778	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575395639	chr12:523787-523788	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183929642	chr12:523796-523797	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542037853	chr12:523829-523830	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs376833546	chr12:523846-523847	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576896797	chr12:523868-523869	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541028304	chr12:523888-523889	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188876416	chr12:523913-523914	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530366653	chr12:523927-523928	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs554156363	chr12:523928-523929	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139864108	chr12:523951-523952	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs199596178	chr12:523952-523953	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375841357	chr12:523955-523956	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542504860	chr12:523960-523961	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145816046	chr12:523962-523963	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531111707	chr12:523975-523976	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552770521	chr12:524016-524017	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570583777	chr12:524017-524018	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs60363415	chr12:524029-524030	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs79826187	chr12:524031-524032	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs373870757	chr12:524042-524043	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs61908460	chr12:524061-524062	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
27	rs535431027	chr12:524079-524080	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557202845	chr12:524105-524106	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568749486	chr12:524113-524114	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539255178	chr12:524121-524122	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75545994	chr12:524123-524124	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs11062845	chr12:524184-524185	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs115138022	chr12:524220-524221	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376579455	chr12:524291-524292	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563522560	chr12:524325-524326	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553121739	chr12:524339-524340	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574773825	chr12:524351-524352	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34080070	chr12:524369-524370	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192992284	chr12:524397-524398	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537501195	chr12:524421-524422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531182938	chr12:524451-524452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546440105	chr12:524459-524460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11062847	chr12:524465-524466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201801403	chr12:524469-524470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11062848	chr12:524470-524471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71858282	chr12:524473-524474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528228750	chr12:524476-524477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200552832	chr12:524479-524480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142409038	chr12:524487-524488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71435005	chr12:524490-524491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Pleomorphic liposarcoma	18784837	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:511600-544600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr12:511800-523800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr12:511800-523800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr12:511800-524000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:512000-545800	Weak transcription	HMEC	breast
6	chr12:512000-549600	Weak transcription	Colon Smooth Muscle	Colon
7	chr12:512200-540200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:512200-557800	Weak transcription	Fetal Heart	heart
9	chr12:512600-528600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:512600-528800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:512600-552200	Weak transcription	Fetal Brain Male	brain
12	chr12:513600-529000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:513600-529800	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:514200-528600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:514200-528800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr12:514400-528800	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr12:514800-528600	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr12:516800-523800	Weak transcription	HSMM	muscle
19	chr12:518000-524600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:518400-528800	Strong transcription	Dnd41	blood
21	chr12:518600-526600	Strong transcription	Fetal Intestine Small	intestine
22	chr12:518600-528400	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr12:518800-529800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:519400-524400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr12:519400-528600	Strong transcription	Fetal Stomach	stomach
26	chr12:519400-529800	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr12:519600-524200	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr12:519600-524400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr12:519600-524400	Strong transcription	Fetal Muscle Leg	muscle
30	chr12:519600-524400	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr12:519600-524600	Strong transcription	Fetal Muscle Trunk	muscle
32	chr12:519600-528600	Strong transcription	Thymus	Thymus
33	chr12:519800-524400	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr12:519800-528600	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr12:519800-528600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr12:519800-528600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr12:519800-528800	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr12:519800-528800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:520000-527800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr12:520400-528600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:520600-523800	Strong transcription	Brain Germinal Matrix	brain
42	chr12:520600-524400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr12:520600-524400	Strong transcription	Stomach Smooth Muscle	stomach
44	chr12:520600-525600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:520800-524200	Strong transcription	Primary T cells from cord blood	blood
46	chr12:520800-524400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr12:520800-524400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr12:520800-524400	Strong transcription	Primary hematopoietic stem cells	blood
49	chr12:520800-524400	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr12:520800-524400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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