Variant report

Variant	nsv526770
Chromosome Location	chr4:142048547-142061946
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:1160)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 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	chr4:142054521-142054900	HepG2	liver:	n/a	n/a
2	ATF2	chr4:142054439-142054937	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:142054497-142054871	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:142053394-142053651	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:142054597-142054905	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:142054649-142054734	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:142054562-142054874	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:142056154-142056251	K562	blood:	n/a	chr4:142056205-142056216 chr4:142056203-142056216 chr4:142056203-142056216
9	CHD1	chr4:142054135-142054302	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr4:142053559-142053752	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr4:142052215-142055039	IMR90	lung:	n/a	chr4:142054128-142054138
12	CHD1	chr4:142053307-142053357	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr4:142054602-142054883	GM12878	blood:	n/a	n/a
14	CHD2	chr4:142053333-142053537	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr4:142054527-142054850	HepG2	liver:	n/a	n/a
16	CHD2	chr4:142054242-142054912	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr4:142054451-142054698	A549	lung:	n/a	n/a
18	CTBP2	chr4:142053107-142054884	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr4:142055340-142055490	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr4:142055260-142055410	SAEC	small airway:	n/a	n/a
21	CTCF	chr4:142052420-142052570	HCFaa	heart:	n/a	n/a
22	CTCF	chr4:142054680-142054830	Caco-2	colon:	n/a	n/a
23	CTCF	chr4:142055320-142055470	HEK293	kidney:	n/a	n/a
24	CTCF	chr4:142054560-142054710	GM12868	blood:	n/a	n/a
25	CTCF	chr4:142054680-142054830	GM12875	blood:	n/a	n/a
26	CTCF	chr4:142054680-142054830	AG04449	skin:	n/a	n/a
27	CTCF	chr4:142054483-142054540	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr4:142054680-142054830	HCT-116	colon:	n/a	n/a
29	CTCF	chr4:142054660-142054810	HAc	cerebellar:	n/a	n/a
30	CTCF	chr4:142054660-142054810	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr4:142054640-142054790	GM12873	blood:	n/a	n/a
32	CTCF	chr4:142054680-142054830	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr4:142054614-142054850	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr4:142053460-142053610	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr4:142055368-142055460	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:142054474-142054494	NHEK	skin:	n/a	n/a
37	CTCF	chr4:142055300-142055450	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr4:142055900-142056050	GM12869	blood:	n/a	n/a
39	CTCF	chr4:142054800-142054950	A549	lung:	n/a	n/a
40	CTCF	chr4:142053427-142055764	SK-N-SH	brain:	n/a	n/a
41	CTCF	chr4:142055403-142055458	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr4:142054459-142054903	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:142054363-142054855	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:142054495-142054873	NHEK	skin:	n/a	n/a
45	CTCF	chr4:142054680-142054830	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr4:142054680-142054830	GM12864	blood:	n/a	n/a
47	CTCF	chr4:142054660-142054810	GM12865	blood:	n/a	n/a
48	CTCF	chr4:142054655-142054840	GM13976	blood:	n/a	n/a
49	CTCF	chr4:142054680-142054830	AG09319	gingival:	n/a	n/a
50	CTCF	chr4:142054640-142054790	GM12801	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:142054743-142054793	HRCEpiC	kidney:	n/a
2	chr4:142054743-142054793	HRCEpiC	kidney:	n/a
3	chr4:142053720-142053770	RPTEC	kidney:	n/a
4	chr4:142054776-142054826	GM12891	blood:	n/a
5	chr4:142054254-142054304	PANC-1	pancreas:	n/a
6	chr4:142054776-142054826	HRPEpiC	eye:	n/a
7	chr4:142053720-142053770	AoSMC	blood vessel:	n/a
8	chr4:142055319-142055369	AG09309	skin:	n/a
9	chr4:142054446-142054496	HEK293	kidney:	embryo
10	chr4:142054779-142054829	HCM	heart:	n/a
11	chr4:142054753-142054803	ProgFib	skin:	n/a
12	chr4:142053623-142053673	PANC-1	pancreas:	n/a
13	chr4:142053970-142054020	HEK293	kidney:	embryo
14	chr4:142054329-142054379	GM12878	blood:	n/a
15	chr4:142054776-142054826	SK-N-SH	brain:	n/a
16	chr4:142049332-142049382	ECC-1	luminal epithelium:	n/a
17	chr4:142054417-142054467	HRPEpiC	eye:	n/a
18	chr4:142053970-142054020	AG09319	gingival:	n/a
19	chr4:142054446-142054496	HRE	kidney:	n/a
20	chr4:142054743-142054793	HCT-116	colon:	n/a
21	chr4:142054446-142054496	MCF10A-Er-Src	breast:	n/a
22	chr4:142054776-142054826	HL-60	blood:	n/a
23	chr4:142053970-142054020	ProgFib	skin:	n/a
24	chr4:142054417-142054467	SAEC	small airway:	n/a
25	chr4:142053146-142053196	AG10803	skin:	n/a
26	chr4:142054818-142054868	AG04450	lung:	fetal
27	chr4:142054660-142054710	IMR90	lung:	fetal
28	chr4:142054753-142054803	PFSK-1	brain:	n/a
29	chr4:142054660-142054710	HAEpiC	amniotic membrane:	n/a
30	chr4:142053720-142053770	HepG2	liver:	n/a
31	chr4:142054878-142054928	MCF-7	breast:	n/a
32	chr4:142054446-142054496	PrEC	prostate:	n/a
33	chr4:142054878-142054928	HepG2	liver:	n/a
34	chr4:142054417-142054467	AG09309	skin:	n/a
35	chr4:142054810-142054860	CMK	blood:	n/a
36	chr4:142055319-142055369	HL-60	blood:	n/a
37	chr4:142054818-142054868	NHBE	bronchial:	n/a
38	chr4:142057832-142057882	CMK	blood:	n/a
39	chr4:142054329-142054379	HRE	kidney:	n/a
40	chr4:142057832-142057882	HMEC	breast:	n/a
41	chr4:142054417-142054467	IMR90	lung:	fetal
42	chr4:142053623-142053673	Hepatocyte	liver:	n/a
43	chr4:142053623-142053673	HMEC	breast:	n/a
44	chr4:142054810-142054860	K562	blood:	n/a
45	chr4:142054329-142054379	SK-N-SH_RA	brain:	n/a
46	chr4:142054878-142054928	NT2-D1	testis:	n/a
47	chr4:142055319-142055369	HCM	heart:	n/a
48	chr4:142049332-142049382	H1-hESC	embryonic stem cell:	embryo
49	chr4:142053970-142054020	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:142054329-142054379	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:142053277..142055129-chr4:142140562..142142669,2	MCF-7	breast:
2	chr4:142053889..142056173-chr4:142056936..142059730,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNF150	TF binding region
RNF150	CpG island
ENSG00000170153	chromatin interactions
ENSG00000109445	chromatin interactions

Extended variants
information (count: 416 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4956518	chr4:142048547-142048548	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112945177	chr4:142048655-142048656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564375024	chr4:142048702-142048703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531826227	chr4:142048829-142048830	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs550046305	chr4:142048879-142048880	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs147819540	chr4:142048939-142048940	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs201946676	chr4:142048961-142048962	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs541807215	chr4:142048991-142048992	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs563312581	chr4:142049002-142049003	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs530494492	chr4:142049089-142049090	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs552276348	chr4:142049096-142049097	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs564110330	chr4:142049097-142049098	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs186884186	chr4:142049116-142049117	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs17341855	chr4:142049118-142049119	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs141360166	chr4:142049148-142049149	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs535368749	chr4:142049225-142049226	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs547655567	chr4:142049265-142049266	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs570062431	chr4:142049275-142049276	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs566047570	chr4:142049361-142049362	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs537135577	chr4:142049367-142049368	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs559051496	chr4:142049380-142049381	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs10001083	chr4:142049408-142049409	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs535181504	chr4:142049457-142049458	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs367904843	chr4:142049458-142049459	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs191508881	chr4:142049503-142049504	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs182357571	chr4:142049600-142049601	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs530554770	chr4:142049702-142049703	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs147009772	chr4:142049778-142049779	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs575230396	chr4:142049828-142049829	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs58050198	chr4:142049845-142049846	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs531353145	chr4:142049871-142049872	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs187899988	chr4:142049898-142049899	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs528173105	chr4:142049916-142049917	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs192479159	chr4:142049960-142049961	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs184898739	chr4:142049975-142049976	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs529131792	chr4:142049988-142049989	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs539603221	chr4:142049993-142049994	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs569943469	chr4:142050010-142050011	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs145137157	chr4:142050029-142050030	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs187997244	chr4:142050030-142050031	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs374183081	chr4:142050044-142050045	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs3897805	chr4:142050045-142050046	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs113404222	chr4:142050086-142050087	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs76468791	chr4:142050087-142050088	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs143003865	chr4:142050120-142050121	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs192086890	chr4:142050149-142050150	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs558334066	chr4:142050180-142050181	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs570201726	chr4:142050199-142050200	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs537938007	chr4:142050207-142050208	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs112840443	chr4:142050242-142050243	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21510904	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142038600-142052600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:142039000-142049200	Weak transcription	Fetal Brain Female	brain
3	chr4:142039400-142051800	Weak transcription	Aorta	Aorta
4	chr4:142041000-142048600	Weak transcription	Adipose Nuclei	Adipose
5	chr4:142041000-142052200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr4:142042600-142048600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr4:142043600-142051800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr4:142044400-142051200	Weak transcription	Osteobl	bone
9	chr4:142044600-142051600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:142044800-142051800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:142045800-142048800	Enhancers	Fetal Heart	heart
12	chr4:142045800-142049000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:142045800-142051200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:142045800-142051200	Weak transcription	Fetal Muscle Trunk	muscle
15	chr4:142047000-142048600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr4:142047200-142048800	Weak transcription	Brain Substantia Nigra	brain
17	chr4:142047200-142049400	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr4:142047200-142050200	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr4:142047400-142048600	Enhancers	Psoas Muscle	Psoas
20	chr4:142047400-142048800	Enhancers	Right Ventricle	heart
21	chr4:142047400-142049000	Enhancers	Stomach Smooth Muscle	stomach
22	chr4:142047400-142049400	Enhancers	Left Ventricle	heart
23	chr4:142047400-142049600	Enhancers	Ovary	ovary
24	chr4:142047600-142048800	Enhancers	Right Atrium	heart
25	chr4:142047600-142049600	Enhancers	Fetal Stomach	stomach
26	chr4:142047600-142050600	Enhancers	Colon Smooth Muscle	Colon
27	chr4:142047800-142048800	Weak transcription	Brain Anterior Caudate	brain
28	chr4:142048000-142048600	Enhancers	Fetal Brain Male	brain
29	chr4:142048200-142049200	Weak transcription	Rectal Smooth Muscle	rectum
30	chr4:142048200-142051800	Weak transcription	Brain Cingulate Gyrus	brain
31	chr4:142048400-142049000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr4:142048400-142049000	Weak transcription	Spleen	Spleen
33	chr4:142048400-142049200	Weak transcription	Lung	lung
34	chr4:142048400-142050400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr4:142048400-142050600	Weak transcription	Fetal Muscle Leg	muscle
36	chr4:142048400-142053000	Weak transcription	Pancreas	Pancrea
37	chr4:142048600-142049000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr4:142048600-142049000	Weak transcription	Fetal Brain Male	brain
39	chr4:142048600-142049000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr4:142048600-142049000	Weak transcription	Psoas Muscle	Psoas
41	chr4:142048600-142049800	Enhancers	Adipose Nuclei	Adipose
42	chr4:142048800-142049000	Enhancers	Brain Substantia Nigra	brain
43	chr4:142048800-142049000	Flanking Active TSS	Fetal Heart	heart
44	chr4:142048800-142049400	Enhancers	Brain Anterior Caudate	brain
45	chr4:142048800-142049400	Enhancers	NHDF-Ad	bronchial
46	chr4:142048800-142050600	Weak transcription	Right Atrium	heart
47	chr4:142048800-142055600	Active TSS	Right Ventricle	heart
48	chr4:142049000-142049200	Enhancers	Fetal Heart	heart
49	chr4:142049000-142049200	Flanking Active TSS	Stomach Smooth Muscle	stomach
50	chr4:142049000-142049400	Active TSS	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links