Variant report

Variant	nsv964147
Chromosome Location	chr4:120326556-120352949
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	BATF	chr4:120336031-120336269	GM12878	blood:	n/a	n/a
2	CEBPB	chr4:120341188-120341402	IMR90	lung:	n/a	chr4:120341261-120341272
3	CEBPB	chr4:120331779-120331807	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:120338250-120338527	K562	blood:	n/a	n/a
5	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
6	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
7	CTCF	chr4:120330551-120330624	Hela-S3	cervix:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
8	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
9	CTCF	chr4:120330540-120330690	GM12875	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
10	CTCF	chr4:120344460-120344610	GM12871	blood:	n/a	n/a
11	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
12	CTCF	chr4:120339549-120339589	GM13976	blood:	n/a	n/a
13	CTCF	chr4:120330801-120330893	MCF-7	breast:	n/a	chr4:120330828-120330846
14	CTCF	chr4:120332000-120332150	HMF	breast:	n/a	n/a
15	CTCF	chr4:120343061-120343106	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr4:120331793-120332011	K562	blood:	n/a	n/a
17	CTCF	chr4:120330528-120330612	Medullo	brain:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
18	CTCF	chr4:120327935-120328268	K562	blood:	n/a	chr4:120327955-120327968
19	CTCF	chr4:120330515-120330644	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
20	CTCF	chr4:120330554-120330558	MCF-7	breast:	n/a	n/a
21	CTCF	chr4:120330761-120330843	GM10266	blood:	n/a	n/a
22	CTCF	chr4:120330858-120330883	GM12891	blood:	n/a	n/a
23	CTCF	chr4:120330780-120330930	AG04449	skin:	n/a	chr4:120330828-120330846
24	CTCF	chr4:120330360-120330510	GM12873	blood:	n/a	n/a
25	CTCF	chr4:120331736-120332064	K562	blood:	n/a	n/a
26	CTCF	chr4:120330524-120330616	GM19238	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
27	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
28	CTCF	chr4:120327406-120327479	GM13976	blood:	n/a	n/a
29	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
30	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
31	CTCF	chr4:120330536-120330625	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
32	CTCF	chr4:120330539-120330631	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
33	CTCF	chr4:120330780-120330930	HepG2	liver:	n/a	chr4:120330828-120330846
34	CTCF	chr4:120331793-120332099	K562	blood:	n/a	n/a
35	CTCF	chr4:120330786-120330880	MCF-7	breast:	n/a	chr4:120330828-120330846
36	CTCF	chr4:120330320-120330470	GM12865	blood:	n/a	n/a
37	CTCF	chr4:120336331-120336394	GM13977	blood:	n/a	n/a
38	CTCF	chr4:120330559-120330616	MCF-7	breast:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
39	CTCF	chr4:120330556-120330618	GM20000	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
40	CTCF	chr4:120327880-120328343	K562	blood:	n/a	chr4:120327955-120327968
41	CTCF	chr4:120330532-120330619	Gliobla	brain:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
42	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
43	CTCF	chr4:120330516-120330632	GM12892	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
44	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
45	CTCF	chr4:120332000-120332150	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr4:120330600-120330870	WERI-Rb-1	eye:	n/a	chr4:120330828-120330846
47	CTCF	chr4:120331980-120332130	RPTEC	kidney:	n/a	n/a
48	CTCF	chr4:120330520-120330629	GM12878	blood:	n/a	chr4:120330572-120330581 chr4:120330571-120330592 chr4:120330569-120330587 chr4:120330574-120330584 chr4:120330572-120330585
49	CTCF	chr4:120330845-120330847	GM10266	blood:	n/a	n/a
50	CTCF	chr4:120331640-120331790	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120328025-120328075	HEK293	kidney:	embryo
2	chr4:120328025-120328075	HEK293	kidney:	embryo
3	chr4:120327182-120327232	AoSMC	blood vessel:	n/a
4	chr4:120328025-120328075	A549	lung:	n/a
5	chr4:120327624-120327674	SK-N-SH_RA	brain:	n/a
6	chr4:120328025-120328075	MCF-7	breast:	n/a
7	chr4:120327182-120327232	IMR90	lung:	fetal
8	chr4:120332083-120332133	HEK293	kidney:	embryo
9	chr4:120327182-120327232	AG04450	lung:	fetal
10	chr4:120327182-120327232	HCF	heart:	n/a
11	chr4:120332083-120332133	SK-N-MC	brain:	n/a
12	chr4:120327624-120327674	NHDF-neo	bronchial:	n/a
13	chr4:120332083-120332133	LNCaP	prostate:	n/a
14	chr4:120327624-120327674	GM06990	blood:	n/a
15	chr4:120329925-120329975	HMEC	breast:	n/a
16	chr4:120328025-120328075	RPTEC	kidney:	n/a
17	chr4:120327182-120327232	HepG2	liver:	n/a
18	chr4:120328025-120328075	HCT-116	colon:	n/a
19	chr4:120328025-120328075	SAEC	small airway:	n/a
20	chr4:120329925-120329975	SK-N-MC	brain:	n/a
21	chr4:120329925-120329975	HCPEpiC	choroid plexus:	n/a
22	chr4:120328025-120328075	HNPCEpiC	eye:	n/a
23	chr4:120327624-120327674	SKMC	muscle:	n/a
24	chr4:120332083-120332133	Hela-S3	cervix:	n/a
25	chr4:120327182-120327232	SK-N-SH_RA	brain:	n/a
26	chr4:120328025-120328075	AoSMC	blood vessel:	n/a
27	chr4:120327182-120327232	ProgFib	skin:	n/a
28	chr4:120332083-120332133	HEEpiC	esophagus:	n/a
29	chr4:120328025-120328075	HCM	heart:	n/a
30	chr4:120327182-120327232	HEK293	kidney:	embryo
31	chr4:120329925-120329975	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:120332083-120332133	GM19239	blood:	n/a
33	chr4:120327182-120327232	U87	brain:	n/a
34	chr4:120332083-120332133	SK-N-SH	brain:	n/a
35	chr4:120327182-120327232	Hela-S3	cervix:	n/a
36	chr4:120327624-120327674	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:120332083-120332133	AG09309	skin:	n/a
38	chr4:120332083-120332133	T-47D	breast:	n/a
39	chr4:120327624-120327674	LNCaP	prostate:	n/a
40	chr4:120327182-120327232	NH-A	brain:	n/a
41	chr4:120329925-120329975	GM12892	blood:	n/a
42	chr4:120329925-120329975	PANC-1	pancreas:	n/a
43	chr4:120328025-120328075	BJ	skin:	n/a
44	chr4:120329925-120329975	NHDF-neo	bronchial:	n/a
45	chr4:120328025-120328075	GM19239	blood:	n/a
46	chr4:120329925-120329975	BE2_C	brain:	n/a
47	chr4:120329925-120329975	Hela-S3	cervix:	n/a
48	chr4:120327624-120327674	ECC-1	luminal epithelium:	n/a
49	chr4:120328025-120328075	LNCaP	prostate:	n/a
50	chr4:120329925-120329975	HEK293	kidney:	embryo

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: 836 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545755080	chr4:120326557-120326558	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564481277	chr4:120326597-120326598	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533444895	chr4:120326598-120326599	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs71610279	chr4:120326643-120326644	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs71610280	chr4:120326648-120326649	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs529403157	chr4:120326661-120326662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548019759	chr4:120326669-120326670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9799664	chr4:120326678-120326679	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs72918577	chr4:120326701-120326702	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs79446934	chr4:120326713-120326714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
11	rs77299866	chr4:120326716-120326717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs539474186	chr4:120326717-120326718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539721540	chr4:120326740-120326741	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs72489565	chr4:120326819-120326820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs572724615	chr4:120326845-120326846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535542094	chr4:120326875-120326876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115044484	chr4:120326887-120326888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs575288460	chr4:120326913-120326914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544450968	chr4:120326922-120326923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564319656	chr4:120326930-120326931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9996586	chr4:120326942-120326943	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs540489250	chr4:120326971-120326972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560135540	chr4:120327027-120327028	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142609610	chr4:120327032-120327033	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs549462614	chr4:120327051-120327052	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562879252	chr4:120327063-120327064	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372821205	chr4:120327068-120327069	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531826432	chr4:120327073-120327074	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550821123	chr4:120327079-120327080	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10019309	chr4:120327085-120327086	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs539768268	chr4:120327092-120327093	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546872502	chr4:120327103-120327104	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566475188	chr4:120327105-120327106	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187857295	chr4:120327118-120327119	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192765835	chr4:120327166-120327167	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs572975570	chr4:120327183-120327184	Weak transcription Enhancers Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs9996865	chr4:120327186-120327187	Weak transcription Enhancers Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	mRNA abundance
38	rs10019421	chr4:120327198-120327199	Weak transcription Enhancers Strong transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs10031129	chr4:120327201-120327202	Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs539199078	chr4:120327237-120327238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559291159	chr4:120327243-120327244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537533571	chr4:120327250-120327251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370990577	chr4:120327271-120327272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575383444	chr4:120327276-120327277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572844941	chr4:120327278-120327279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540527989	chr4:120327282-120327283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560582773	chr4:120327292-120327293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574263598	chr4:120327304-120327305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542699806	chr4:120327305-120327306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562876696	chr4:120327312-120327313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Breast cancer	22522925	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

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	chr4:120324600-120328000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr4:120324600-120330400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr4:120325000-120329800	Weak transcription	Liver	Liver
6	chr4:120325000-120331400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr4:120325000-120331800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:120325000-120341200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:120325200-120334200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:120325600-120326600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:120325600-120326600	Strong transcription	Fetal Stomach	stomach
12	chr4:120326000-120327200	Strong transcription	Fetal Intestine Small	intestine
13	chr4:120326600-120329000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:120326600-120329800	Weak transcription	Fetal Stomach	stomach
15	chr4:120326600-120331600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:120326600-120334400	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr4:120326600-120360800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:120326800-120331600	Weak transcription	Fetal Muscle Leg	muscle
19	chr4:120327000-120327200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:120327000-120328600	Weak transcription	Lung	lung
21	chr4:120327000-120329800	Weak transcription	Gastric	stomach
22	chr4:120327200-120335200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:120327200-120339200	Weak transcription	Esophagus	oesophagus
24	chr4:120327200-120361400	Weak transcription	Fetal Intestine Small	intestine
25	chr4:120327800-120332000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr4:120328000-120329600	Enhancers	Placenta	Placenta
27	chr4:120328000-120330200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr4:120328200-120329800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr4:120328200-120329800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:120328600-120329000	Strong transcription	Lung	lung
31	chr4:120328800-120331400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:120328800-120375200	Weak transcription	Ovary	ovary
33	chr4:120329000-120329800	Weak transcription	Lung	lung
34	chr4:120329200-120331400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr4:120329600-120330600	Genic enhancers	Placenta	Placenta
36	chr4:120329800-120330200	Strong transcription	Lung	lung
37	chr4:120329800-120330400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:120329800-120330400	Strong transcription	Gastric	stomach
39	chr4:120329800-120330600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:120329800-120330600	Strong transcription	Liver	Liver
41	chr4:120329800-120330600	Strong transcription	Fetal Stomach	stomach
42	chr4:120330000-120330600	Enhancers	Adipose Nuclei	Adipose
43	chr4:120330200-120332600	Weak transcription	Lung	lung
44	chr4:120330200-120367600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr4:120330400-120332000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:120330400-120333200	Weak transcription	Gastric	stomach
47	chr4:120330600-120331600	Weak transcription	Placenta	Placenta
48	chr4:120330600-120341400	Weak transcription	Adipose Nuclei	Adipose
49	chr4:120330600-120355400	Weak transcription	Liver	Liver
50	chr4:120330600-120365200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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