Variant report

Variant	nsv525456
Chromosome Location	chr12:48366449-48376969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:32 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:48375432-48375854	K562	blood:	n/a	n/a
2	CTCF	chr12:48373085-48373209	HepG2	liver:	n/a	chr12:48373169-48373178 chr12:48373166-48373184 chr12:48373169-48373182
3	CTCF	chr12:48370640-48370790	HepG2	liver:	n/a	n/a
4	CTCF	chr12:48373111-48373213	Hela-S3	cervix:	n/a	chr12:48373169-48373178 chr12:48373166-48373184 chr12:48373169-48373182
5	CTCF	chr12:48373120-48373270	AG04449	skin:	n/a	chr12:48373169-48373178 chr12:48373166-48373184 chr12:48373169-48373182
6	CTCF	chr12:48373060-48373210	K562	blood:	n/a	chr12:48373169-48373178 chr12:48373166-48373184 chr12:48373169-48373182
7	CTCF	chr12:48373125-48373203	MCF-7	breast:	n/a	chr12:48373169-48373178 chr12:48373166-48373184 chr12:48373169-48373182
8	CTCF	chr12:48373080-48373230	Caco-2	colon:	n/a	chr12:48373169-48373178 chr12:48373166-48373184 chr12:48373169-48373182
9	CTCF	chr12:48373152-48373182	K562	blood:	n/a	chr12:48373169-48373178 chr12:48373169-48373182
10	E2F6	chr12:48375566-48375687	K562	blood:	n/a	n/a
11	EGR1	chr12:48369829-48370058	K562	blood:	n/a	n/a
12	EGR1	chr12:48374016-48374223	K562	blood:	n/a	chr12:48374095-48374110 chr12:48374096-48374109 chr12:48374096-48374109 chr12:48374097-48374107
13	ELK1	chr12:48372194-48372328	Hela-S3	cervix:	n/a	n/a
14	FOXA1	chr12:48366318-48366819	T-47D	breast:	n/a	n/a
15	FOXA1	chr12:48375125-48375521	HepG2	liver:	n/a	chr12:48375350-48375362
16	FOXA1	chr12:48366367-48366822	T-47D	breast:	n/a	n/a
17	FOXA1	chr12:48366444-48366859	HepG2	liver:	n/a	n/a
18	FOXA2	chr12:48375195-48375461	HepG2	liver:	n/a	chr12:48375350-48375362
19	FOXA2	chr12:48366351-48366749	HepG2	liver:	n/a	n/a
20	HMGN3	chr12:48370804-48370825	K562	blood:	n/a	n/a
21	MAX	chr12:48375366-48375547	K562	blood:	n/a	n/a
22	MAX	chr12:48375316-48375824	K562	blood:	n/a	n/a
23	MAZ	chr12:48375219-48375307	HepG2	liver:	n/a	n/a
24	MAZ	chr12:48375404-48375523	K562	blood:	n/a	n/a
25	MAZ	chr12:48373128-48373232	K562	blood:	n/a	n/a
26	MYC	chr12:48371343-48371349	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr12:48375617-48375650	Gliobla	brain:	n/a	n/a
28	REST	chr12:48373089-48373329	K562	blood:	n/a	chr12:48373234-48373247
29	RFX5	chr12:48375191-48375203	HepG2	liver:	n/a	n/a
30	ZBTB7A	chr12:48375290-48375415	K562	blood:	n/a	n/a
31	ZNF263	chr12:48372682-48373169	HEK293-T-REx	kidney:	n/a	chr12:48372793-48372814 chr12:48372804-48372813
32	ZNF274	chr12:48372250-48372777	NT2-D1	testis:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48367161-48367211	HRPEpiC	eye:	n/a
2	chr12:48367161-48367211	IMR90	lung:	fetal
3	chr12:48375673-48375723	HCM	heart:	n/a
4	chr12:48367161-48367211	HL-60	blood:	n/a
5	chr12:48367161-48367211	GM19239	blood:	n/a
6	chr12:48375673-48375723	HIPEpiC	eye:	n/a
7	chr12:48367161-48367211	NHBE	bronchial:	n/a
8	chr12:48375673-48375723	Caco-2	colon:	n/a
9	chr12:48367161-48367211	HNPCEpiC	eye:	n/a
10	chr12:48375673-48375723	HRE	kidney:	n/a
11	chr12:48367161-48367211	MCF-7	breast:	n/a
12	chr12:48367161-48367211	GM12892	blood:	n/a
13	chr12:48367161-48367211	PANC-1	pancreas:	n/a
14	chr12:48367161-48367211	Jurkat	blood:	n/a
15	chr12:48367161-48367211	K562	blood:	n/a
16	chr12:48375673-48375723	Hepatocyte	liver:	n/a
17	chr12:48375673-48375723	AG09319	gingival:	n/a
18	chr12:48367161-48367211	SK-N-SH_RA	brain:	n/a
19	chr12:48375673-48375723	Hela-S3	cervix:	n/a
20	chr12:48375673-48375723	AG04449	skin:	fetal
21	chr12:48375673-48375723	HL-60	blood:	n/a
22	chr12:48367161-48367211	HCPEpiC	choroid plexus:	n/a
23	chr12:48367161-48367211	HCT-116	colon:	n/a
24	chr12:48375673-48375723	MCF10A-Er-Src	breast:	n/a
25	chr12:48367161-48367211	MCF10A-Er-Src	breast:	n/a
26	chr12:48367161-48367211	AoSMC	blood vessel:	n/a
27	chr12:48375673-48375723	MCF-7	breast:	n/a
28	chr12:48375673-48375723	HEEpiC	esophagus:	n/a
29	chr12:48367161-48367211	AG09309	skin:	n/a
30	chr12:48375673-48375723	HNPCEpiC	eye:	n/a
31	chr12:48367161-48367211	AG10803	skin:	n/a
32	chr12:48367161-48367211	HAEpiC	amniotic membrane:	n/a
33	chr12:48367161-48367211	NH-A	brain:	n/a
34	chr12:48375673-48375723	AG09309	skin:	n/a
35	chr12:48375673-48375723	GM12878	blood:	n/a
36	chr12:48367161-48367211	NHDF-neo	bronchial:	n/a
37	chr12:48375673-48375723	SAEC	small airway:	n/a
38	chr12:48367161-48367211	ProgFib	skin:	n/a
39	chr12:48375673-48375723	Jurkat	blood:	n/a
40	chr12:48375673-48375723	IMR90	lung:	fetal
41	chr12:48367161-48367211	HIPEpiC	eye:	n/a
42	chr12:48367161-48367211	GM12878	blood:	n/a
43	chr12:48375673-48375723	T-47D	breast:	n/a
44	chr12:48367161-48367211	LNCaP	prostate:	n/a
45	chr12:48367161-48367211	HUVEC	blood vessel:	n/a
46	chr12:48375673-48375723	PANC-1	pancreas:	n/a
47	chr12:48367161-48367211	HEEpiC	esophagus:	n/a
48	chr12:48375673-48375723	GM19239	blood:	n/a
49	chr12:48375673-48375723	NHDF-neo	bronchial:	n/a
50	chr12:48375673-48375723	GM12892	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:48370423..48373200-chr12:48373445..48376245,2	K562	blood:
2	chr12:48360838..48363620-chr12:48364578..48367184,3	K562	blood:
3	chr12:48373823..48376376-chr12:48383731..48387007,3	MCF-7	breast:
4	chr12:48246296..48248237-chr12:48373548..48375566,2	MCF-7	breast:
5	chr12:48366900..48369507-chr12:48392554..48394762,2	MCF-7	breast:
6	chr12:48366493..48369414-chr12:48372046..48373592,2	K562	blood:
7	chr12:48366493..48369414-chr12:48372046..48373592,2	K562	blood:
8	chr12:48365132..48368005-chr12:48368353..48370036,2	K562	blood:
9	chr12:48362502..48365466-chr12:48366201..48368271,2	K562	blood:
10	chr12:48375228..48376777-chr12:48381596..48383195,2	MCF-7	breast:
11	chr12:48262428..48264401-chr12:48374730..48377595,2	K562	blood:
12	chr12:48372717..48377052-chr12:48391617..48394178,3	MCF-7	breast:
13	chr12:48293420..48296418-chr12:48372974..48374777,2	K562	blood:
14	chr12:48375713..48377256-chr12:48377465..48379370,2	MCF-7	breast:
15	chr12:48365132..48368005-chr12:48368353..48370036,2	K562	blood:
16	chr12:48366898..48369197-chr12:48592697..48594577,2	K562	blood:

No data

Variant related genes	Relation type
COL2A1	TF binding region
COL2A1	CpG island
ENSG00000139219	chromatin interactions

Extended variants
information (count: 639 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2071358	chr12:48366449-48366450	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs151325424	chr12:48366481-48366482	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs577095579	chr12:48366486-48366487	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs140566186	chr12:48366496-48366497	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs562609183	chr12:48366521-48366522	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs191023375	chr12:48366524-48366525	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs2071357	chr12:48366547-48366548	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs2071356	chr12:48366550-48366551	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs527425557	chr12:48366578-48366579	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs183216562	chr12:48366600-48366601	Strong transcription Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs570740533	chr12:48366618-48366619	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76729841	chr12:48366644-48366645	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550464562	chr12:48366678-48366679	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570211999	chr12:48366783-48366784	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559491246	chr12:48366869-48366870	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532700241	chr12:48366885-48366886	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs41272781	chr12:48366895-48366896	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572459859	chr12:48366911-48366912	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535153980	chr12:48366924-48366925	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558260275	chr12:48366955-48366956	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547674883	chr12:48366993-48366994	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs41272779	chr12:48367004-48367005	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs147803471	chr12:48367050-48367051	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs41272777	chr12:48367054-48367055	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs370163304	chr12:48367092-48367093	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576307978	chr12:48367093-48367094	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs41272775	chr12:48367162-48367163	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs369207030	chr12:48367172-48367173	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs41272773	chr12:48367186-48367187	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs41272771	chr12:48367205-48367206	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376442872	chr12:48367206-48367207	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs369696920	chr12:48367232-48367233	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540750398	chr12:48367234-48367235	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145524810	chr12:48367274-48367275	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs148838496	chr12:48367279-48367280	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs137948104	chr12:48367304-48367305	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs113238468	chr12:48367306-48367307	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200214562	chr12:48367310-48367311	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78690642	chr12:48367327-48367328	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201223454	chr12:48367328-48367329	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs570227994	chr12:48367353-48367354	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529600168	chr12:48367368-48367369	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375905906	chr12:48367371-48367372	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372534127	chr12:48367375-48367376	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375822702	chr12:48367381-48367382	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs61048429	chr12:48367427-48367428	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs7310398	chr12:48367428-48367429	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186469070	chr12:48367435-48367436	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558294986	chr12:48367465-48367466	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs139902658	chr12:48367466-48367467	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	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
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48358400-48367800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:48358400-48367800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:48358400-48369800	Weak transcription	Brain Angular Gyrus	brain
4	chr12:48358400-48373000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:48358600-48366600	Weak transcription	Fetal Lung	lung
6	chr12:48358600-48369400	Weak transcription	Fetal Kidney	kidney
7	chr12:48358600-48381400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:48359200-48384000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr12:48359600-48366600	Strong transcription	Thymus	Thymus
10	chr12:48360000-48368200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr12:48360200-48369600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr12:48362200-48368000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr12:48362400-48370600	Weak transcription	HMEC	breast
14	chr12:48362400-48370800	Weak transcription	NHEK	skin
15	chr12:48362600-48367200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:48362800-48367600	Weak transcription	Small Intestine	intestine
17	chr12:48362800-48368000	Weak transcription	Fetal Brain Female	brain
18	chr12:48363000-48367000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr12:48363000-48367800	Weak transcription	Colon Smooth Muscle	Colon
20	chr12:48363000-48368800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr12:48363000-48370800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:48363000-48370800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:48363200-48370800	Weak transcription	Fetal Stomach	stomach
24	chr12:48363400-48366600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr12:48363400-48366600	Weak transcription	Pancreas	Pancrea
26	chr12:48363400-48367800	Weak transcription	Dnd41	blood
27	chr12:48363400-48368200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr12:48363400-48368200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr12:48363400-48369000	Weak transcription	Fetal Muscle Trunk	muscle
30	chr12:48363400-48370800	Weak transcription	Fetal Thymus	thymus
31	chr12:48363400-48374800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr12:48363400-48375000	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr12:48363400-48375000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr12:48363400-48383000	Weak transcription	Spleen	Spleen
35	chr12:48364000-48370600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:48364400-48369800	Weak transcription	Stomach Smooth Muscle	stomach
37	chr12:48364400-48371600	Weak transcription	Fetal Muscle Leg	muscle
38	chr12:48364400-48372600	Strong transcription	Fetal Intestine Small	intestine
39	chr12:48364400-48381200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:48364600-48369800	Weak transcription	Placenta	Placenta
41	chr12:48364800-48368200	Weak transcription	Primary T cells from cord blood	blood
42	chr12:48365000-48367800	Weak transcription	Fetal Intestine Large	intestine
43	chr12:48365200-48381600	Weak transcription	Right Atrium	heart
44	chr12:48365400-48381000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr12:48366000-48366600	Enhancers	Gastric	stomach
46	chr12:48366000-48366600	Enhancers	Stomach Mucosa	stomach
47	chr12:48366000-48366800	Enhancers	HepG2	liver
48	chr12:48366000-48370400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr12:48366200-48370600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr12:48366200-48381200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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