Variant report

Variant	esv3382283
Chromosome Location	chr4:120328454-120331452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr4:120330559-120330616	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
2	CTCF	chr4:120330520-120330629	GM12878	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
3	CTCF	chr4:120330551-120330624	Hela-S3	cervix:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
4	CTCF	chr4:120330489-120330665	K562	blood:	n/a	chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
5	CTCF	chr4:120330556-120330618	GM20000	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
6	CTCF	chr4:120330491-120330633	GM19240	blood:	n/a	chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
7	CTCF	chr4:120330536-120330625	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
8	CTCF	chr4:120330761-120330843	GM10266	blood:	n/a	n/a
9	CTCF	chr4:120330539-120330631	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
10	CTCF	chr4:120330786-120330880	MCF-7	breast:	n/a	chr4:120330828-120330846
11	CTCF	chr4:120330516-120330632	GM12892	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
12	CTCF	chr4:120330858-120330883	GM12891	blood:	n/a	n/a
13	CTCF	chr4:120330360-120330510	GM12873	blood:	n/a	n/a
14	CTCF	chr4:120330528-120330612	Medullo	brain:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
15	CTCF	chr4:120330524-120330616	GM19238	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
16	CTCF	chr4:120330600-120330870	WERI-Rb-1	eye:	n/a	chr4:120330828-120330846
17	CTCF	chr4:120330554-120330558	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:120330503-120330637	HepG2	liver:	n/a	chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
19	CTCF	chr4:120330780-120330930	HepG2	liver:	n/a	chr4:120330828-120330846
20	CTCF	chr4:120330845-120330847	GM10266	blood:	n/a	n/a
21	CTCF	chr4:120330509-120330630	H1-hESC	embryonic stem cell:	n/a	chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
22	CTCF	chr4:120330780-120330930	AG04449	skin:	n/a	chr4:120330828-120330846
23	CTCF	chr4:120330283-120331115	K562	blood:	n/a	chr4:120330828-120330846 chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
24	CTCF	chr4:120330801-120330893	MCF-7	breast:	n/a	chr4:120330828-120330846
25	CTCF	chr4:120330391-120331008	K562	blood:	n/a	chr4:120330828-120330846 chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
26	CTCF	chr4:120330540-120330690	GM12875	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
27	CTCF	chr4:120330511-120330638	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
28	CTCF	chr4:120330320-120330470	GM12865	blood:	n/a	n/a
29	CTCF	chr4:120330515-120330644	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
30	CTCF	chr4:120330373-120330890	K562	blood:	n/a	chr4:120330828-120330846 chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
31	CTCF	chr4:120330532-120330619	Gliobla	brain:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
32	CTCF	chr4:120330503-120330632	GM12891	blood:	n/a	chr4:120330572-120330581 chr4:120330513-120330526 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
33	FOSL2	chr4:120328108-120328957	HepG2	liver:	n/a	chr4:120328580-120328587
34	FOSL2	chr4:120329667-120330001	HepG2	liver:	n/a	n/a
35	FOSL2	chr4:120329212-120329499	HepG2	liver:	n/a	n/a
36	POLR2A	chr4:120330666-120330746	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr4:120328841-120328879	HUVEC	blood vessel:	n/a	n/a
38	TCF12	chr4:120329013-120329183	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120329925-120329975	AG09309	skin:	n/a
2	chr4:120329925-120329975	HEEpiC	esophagus:	n/a
3	chr4:120329925-120329975	GM19239	blood:	n/a
4	chr4:120329925-120329975	SKMC	muscle:	n/a
5	chr4:120329925-120329975	HEK293	kidney:	embryo
6	chr4:120329925-120329975	HNPCEpiC	eye:	n/a
7	chr4:120329925-120329975	NB4	blood:	n/a
8	chr4:120329925-120329975	NT2-D1	testis:	n/a
9	chr4:120329925-120329975	ProgFib	skin:	n/a
10	chr4:120329925-120329975	MCF10A-Er-Src	breast:	n/a
11	chr4:120329925-120329975	LNCaP	prostate:	n/a
12	chr4:120329925-120329975	HCPEpiC	choroid plexus:	n/a
13	chr4:120329925-120329975	RPTEC	kidney:	n/a
14	chr4:120329925-120329975	AG04450	lung:	fetal
15	chr4:120329925-120329975	BE2_C	brain:	n/a
16	chr4:120329925-120329975	SAEC	small airway:	n/a
17	chr4:120329925-120329975	Caco-2	colon:	n/a
18	chr4:120329925-120329975	H1-hESC	embryonic stem cell:	embryo
19	chr4:120329925-120329975	K562	blood:	n/a
20	chr4:120329925-120329975	NHBE	bronchial:	n/a
21	chr4:120329925-120329975	PANC-1	pancreas:	n/a
22	chr4:120329925-120329975	Jurkat	blood:	n/a
23	chr4:120329925-120329975	HAEpiC	amniotic membrane:	n/a
24	chr4:120329925-120329975	SK-N-SH	brain:	n/a
25	chr4:120329925-120329975	AG04449	skin:	fetal
26	chr4:120329925-120329975	ECC-1	luminal epithelium:	n/a
27	chr4:120329925-120329975	A549	lung:	n/a
28	chr4:120329925-120329975	PrEC	prostate:	n/a
29	chr4:120329925-120329975	HRPEpiC	eye:	n/a
30	chr4:120329925-120329975	HL-60	blood:	n/a
31	chr4:120329925-120329975	HRE	kidney:	n/a
32	chr4:120329925-120329975	NHDF-neo	bronchial:	n/a
33	chr4:120329925-120329975	GM12892	blood:	n/a
34	chr4:120329925-120329975	NH-A	brain:	n/a
35	chr4:120329925-120329975	HMEC	breast:	n/a
36	chr4:120329925-120329975	Hela-S3	cervix:	n/a
37	chr4:120329925-120329975	IMR90	lung:	fetal
38	chr4:120329925-120329975	HCF	heart:	n/a
39	chr4:120329925-120329975	U87	brain:	n/a
40	chr4:120329925-120329975	AG10803	skin:	n/a
41	chr4:120329925-120329975	HIPEpiC	eye:	n/a
42	chr4:120329925-120329975	PFSK-1	brain:	n/a
43	chr4:120329925-120329975	Hepatocyte	liver:	n/a
44	chr4:120329925-120329975	HRCEpiC	kidney:	n/a
45	chr4:120329925-120329975	AoSMC	blood vessel:	n/a
46	chr4:120329925-120329975	SK-N-SH_RA	brain:	n/a
47	chr4:120329925-120329975	SK-N-MC	brain:	n/a
48	chr4:120329925-120329975	GM12878	blood:	n/a
49	chr4:120329925-120329975	MCF-7	breast:	n/a
50	chr4:120329925-120329975	AG09319	gingival:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-2	chr4:120330489-120331408	NONHSAT098058
2	lnc-AC110373.1-2	chr4:120330488-120331388	ENSG00000260091.1

Variant related genes	Relation type
ENSG00000260091	TF binding region
ENSG00000260091	CpG island

Extended variants
information (count: 179 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575803010	chr4:120328461-120328462	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs544912682	chr4:120328462-120328463	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs70944869	chr4:120328463-120328464	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs564878164	chr4:120328465-120328466	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs572248378	chr4:120328476-120328477	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs148377496	chr4:120328477-120328478	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs560709453	chr4:120328494-120328495	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs373934901	chr4:120328500-120328501	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs187720945	chr4:120328510-120328511	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs371873699	chr4:120328511-120328512	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs549875960	chr4:120328516-120328517	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs7654984	chr4:120328520-120328521	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs532710862	chr4:120328569-120328570	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs552793087	chr4:120328593-120328594	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs566408077	chr4:120328594-120328595	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs7655177	chr4:120328622-120328623	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
17	rs548598634	chr4:120328645-120328646	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs71247730	chr4:120328648-120328649	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7655723	chr4:120328666-120328667	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs10023107	chr4:120328669-120328670	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs570603238	chr4:120328672-120328673	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs538493747	chr4:120328677-120328678	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs558309715	chr4:120328680-120328681	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs572338988	chr4:120328709-120328710	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs10034691	chr4:120328726-120328727	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs554574731	chr4:120328771-120328772	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs574308052	chr4:120328776-120328777	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs543554117	chr4:120328781-120328782	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs563412225	chr4:120328805-120328806	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs532240161	chr4:120328827-120328828	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs546445810	chr4:120328845-120328846	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs559673237	chr4:120328874-120328875	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs528797518	chr4:120328878-120328879	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs143810032	chr4:120328894-120328895	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568443601	chr4:120328898-120328899	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs560530912	chr4:120328905-120328906	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs192597348	chr4:120328907-120328908	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs183106090	chr4:120328931-120328932	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs570639519	chr4:120328937-120328938	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs539531048	chr4:120328959-120328960	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558735120	chr4:120328960-120328961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565712490	chr4:120328976-120328977	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534922612	chr4:120328980-120328981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554528904	chr4:120329012-120329013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574772490	chr4:120329092-120329093	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs71610282	chr4:120329093-120329094	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs28552853	chr4:120329126-120329127	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs577044497	chr4:120329140-120329141	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs368921677	chr4:120329175-120329176	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs13130861	chr4:120329207-120329208	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	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
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120318000-120333400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:120324200-120342200	Weak transcription	Pancreas	Pancrea
3	chr4:120324600-120330400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr4:120325000-120329800	Weak transcription	Liver	Liver
5	chr4:120325000-120331400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr4:120325000-120331800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:120325000-120341200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:120325200-120334200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr4:120326600-120329000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr4:120326600-120329800	Weak transcription	Fetal Stomach	stomach
11	chr4:120326600-120331600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:120326600-120334400	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr4:120326600-120360800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:120326800-120331600	Weak transcription	Fetal Muscle Leg	muscle
15	chr4:120327000-120328600	Weak transcription	Lung	lung
16	chr4:120327000-120329800	Weak transcription	Gastric	stomach
17	chr4:120327200-120335200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:120327200-120339200	Weak transcription	Esophagus	oesophagus
19	chr4:120327200-120361400	Weak transcription	Fetal Intestine Small	intestine
20	chr4:120327800-120332000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr4:120328000-120329600	Enhancers	Placenta	Placenta
22	chr4:120328000-120330200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr4:120328200-120329800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:120328200-120329800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:120328600-120329000	Strong transcription	Lung	lung
26	chr4:120328800-120331400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:120328800-120375200	Weak transcription	Ovary	ovary
28	chr4:120329000-120329800	Weak transcription	Lung	lung
29	chr4:120329200-120331400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr4:120329600-120330600	Genic enhancers	Placenta	Placenta
31	chr4:120329800-120330200	Strong transcription	Lung	lung
32	chr4:120329800-120330400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:120329800-120330400	Strong transcription	Gastric	stomach
34	chr4:120329800-120330600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr4:120329800-120330600	Strong transcription	Liver	Liver
36	chr4:120329800-120330600	Strong transcription	Fetal Stomach	stomach
37	chr4:120330000-120330600	Enhancers	Adipose Nuclei	Adipose
38	chr4:120330200-120332600	Weak transcription	Lung	lung
39	chr4:120330200-120367600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr4:120330400-120332000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr4:120330400-120333200	Weak transcription	Gastric	stomach
42	chr4:120330600-120331600	Weak transcription	Placenta	Placenta
43	chr4:120330600-120341400	Weak transcription	Adipose Nuclei	Adipose
44	chr4:120330600-120355400	Weak transcription	Liver	Liver
45	chr4:120330600-120365200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr4:120330600-120366400	Weak transcription	Fetal Stomach	stomach

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