Variant report

Variant	nsv966478
Chromosome Location	chr4:110985403-110995212
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	ARID3A	chr4:110985490-110985821	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:110986172-110986215	K562	blood:	n/a	n/a
3	BHLHE40	chr4:110991725-110991942	K562	blood:	n/a	n/a
4	CEBPB	chr4:110985541-110985750	HepG2	liver:	n/a	chr4:110985675-110985686
5	CEBPB	chr4:110985453-110986046	HepG2	liver:	n/a	chr4:110985675-110985686
6	CEBPB	chr4:110985467-110985795	HepG2	liver:	n/a	chr4:110985675-110985686
7	CEBPB	chr4:110985499-110985850	K562	blood:	n/a	chr4:110985675-110985686
8	CEBPB	chr4:110985507-110985778	K562	blood:	n/a	chr4:110985675-110985686
9	CEBPB	chr4:110985508-110985857	MCF-7	breast:	n/a	chr4:110985675-110985686
10	CEBPB	chr4:110985511-110985799	Hela-S3	cervix:	n/a	chr4:110985675-110985686
11	CEBPB	chr4:110985512-110985836	IMR90	lung:	n/a	chr4:110985675-110985686
12	CEBPB	chr4:110985478-110985826	K562	blood:	n/a	chr4:110985675-110985686
13	CTCF	chr4:110994300-110994450	K562	blood:	n/a	n/a
14	EP300	chr4:110985571-110985672	K562	blood:	n/a	n/a
15	EP300	chr4:110985448-110985779	HepG2	liver:	n/a	n/a
16	EP300	chr4:110985438-110985825	HepG2	liver:	n/a	n/a
17	EP300	chr4:110985594-110985771	HepG2	liver:	n/a	n/a
18	ESR1	chr4:110992481-110992874	ECC-1	luminal epithelium:	n/a	n/a
19	FOXA1	chr4:110985413-110985781	HepG2	liver:	n/a	n/a
20	FOXA1	chr4:110985467-110985780	HepG2	liver:	n/a	n/a
21	FOXA1	chr4:110985396-110985801	HepG2	liver:	n/a	n/a
22	FOXA1	chr4:110985382-110985802	HepG2	liver:	n/a	n/a
23	FOXA2	chr4:110985468-110985751	HepG2	liver:	n/a	n/a
24	GATA1	chr4:110993933-110994857	PBDE	blood:	n/a	chr4:110994119-110994128 chr4:110994119-110994128
25	GATA2	chr4:110987174-110987609	SH-SY5Y	brain:	n/a	chr4:110987328-110987344 chr4:110987331-110987340
26	GATA2	chr4:110989466-110990019	SH-SY5Y	brain:	n/a	n/a
27	GATA2	chr4:110985522-110985820	SH-SY5Y	brain:	n/a	n/a
28	GATA2	chr4:110994260-110994528	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr4:110985399-110985816	MCF-7	breast:	n/a	n/a
30	GATA3	chr4:110985577-110985718	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr4:110989280-110989980	SK-N-SH	brain:	n/a	chr4:110989326-110989336 chr4:110989328-110989338 chr4:110989326-110989335 chr4:110989328-110989335
32	GATA3	chr4:110987009-110987465	SH-SY5Y	brain:	n/a	chr4:110987328-110987344 chr4:110987331-110987340
33	GATA3	chr4:110985550-110985773	MCF-7	breast:	n/a	n/a
34	GATA3	chr4:110989258-110989879	SH-SY5Y	brain:	n/a	chr4:110989326-110989336 chr4:110989328-110989338 chr4:110989326-110989335 chr4:110989328-110989335
35	GATA3	chr4:110989158-110990112	SK-N-SH	brain:	n/a	chr4:110989326-110989336 chr4:110989328-110989338 chr4:110989326-110989335 chr4:110989328-110989335
36	GATA3	chr4:110987087-110987541	MCF-7	breast:	n/a	chr4:110987328-110987344 chr4:110987331-110987340
37	HDAC2	chr4:110985516-110985818	HepG2	liver:	n/a	n/a
38	HNF4A	chr4:110985403-110985891	HepG2	liver:	n/a	n/a
39	HNF4A	chr4:110985476-110985782	HepG2	liver:	n/a	n/a
40	MXI1	chr4:110985515-110985584	HepG2	liver:	n/a	n/a
41	MXI1	chr4:110993987-110994712	SK-N-SH	brain:	n/a	n/a
42	NFIC	chr4:110992567-110993037	ECC-1	luminal epithelium:	n/a	chr4:110992829-110992846
43	NFIC	chr4:110989386-110990037	SK-N-SH	brain:	n/a	n/a
44	NFYB	chr4:110991793-110992003	K562	blood:	n/a	n/a
45	NR2F2	chr4:110987035-110987566	MCF-7	breast:	n/a	n/a
46	PBX3	chr4:110989483-110989991	SK-N-SH	brain:	n/a	n/a
47	POLR2A	chr4:110994182-110995084	K562	blood:	n/a	n/a
48	POLR2A	chr4:110989970-110990097	K562	blood:	n/a	n/a
49	POLR2A	chr4:110993710-110993865	K562	blood:	n/a	n/a
50	POLR2A	chr4:110991038-110991058	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110992869-110992919	SK-N-SH_RA	brain:	n/a
2	chr4:110992869-110992919	U87	brain:	n/a
3	chr4:110992869-110992919	HRE	kidney:	n/a
4	chr4:110992869-110992919	BJ	skin:	n/a
5	chr4:110992869-110992919	HMEC	breast:	n/a
6	chr4:110992869-110992919	PrEC	prostate:	n/a
7	chr4:110992869-110992919	MCF10A-Er-Src	breast:	n/a
8	chr4:110992869-110992919	HCF	heart:	n/a
9	chr4:110992869-110992919	AG10803	skin:	n/a
10	chr4:110992869-110992919	NH-A	brain:	n/a
11	chr4:110992869-110992919	BE2_C	brain:	n/a
12	chr4:110992869-110992919	GM19239	blood:	n/a
13	chr4:110992869-110992919	ECC-1	luminal epithelium:	n/a
14	chr4:110992869-110992919	AG09319	gingival:	n/a
15	chr4:110992869-110992919	ProgFib	skin:	n/a
16	chr4:110992869-110992919	CMK	blood:	n/a
17	chr4:110992869-110992919	K562	blood:	n/a
18	chr4:110992869-110992919	PFSK-1	brain:	n/a
19	chr4:110992869-110992919	AG09309	skin:	n/a
20	chr4:110992869-110992919	Hepatocyte	liver:	n/a
21	chr4:110992869-110992919	PANC-1	pancreas:	n/a
22	chr4:110992869-110992919	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:110992869-110992919	NHBE	bronchial:	n/a
24	chr4:110992869-110992919	T-47D	breast:	n/a
25	chr4:110992869-110992919	HUVEC	blood vessel:	n/a
26	chr4:110992869-110992919	AG04449	skin:	fetal
27	chr4:110992869-110992919	GM06990	blood:	n/a
28	chr4:110992869-110992919	IMR90	lung:	fetal
29	chr4:110992869-110992919	MCF-7	breast:	n/a
30	chr4:110992869-110992919	A549	lung:	n/a
31	chr4:110992869-110992919	HIPEpiC	eye:	n/a
32	chr4:110992869-110992919	GM12891	blood:	n/a
33	chr4:110992869-110992919	GM12878	blood:	n/a
34	chr4:110992869-110992919	SK-N-SH	brain:	n/a
35	chr4:110992869-110992919	AoSMC	blood vessel:	n/a
36	chr4:110992869-110992919	HEEpiC	esophagus:	n/a
37	chr4:110992869-110992919	NT2-D1	testis:	n/a
38	chr4:110992869-110992919	Jurkat	blood:	n/a
39	chr4:110992869-110992919	HAEpiC	amniotic membrane:	n/a
40	chr4:110992869-110992919	NHDF-neo	bronchial:	n/a
41	chr4:110992869-110992919	HCPEpiC	choroid plexus:	n/a
42	chr4:110992869-110992919	ovcar-3	ovarian:	n/a
43	chr4:110992869-110992919	AG04450	lung:	fetal
44	chr4:110992869-110992919	HEK293	kidney:	embryo
45	chr4:110992869-110992919	SAEC	small airway:	n/a
46	chr4:110992869-110992919	NB4	blood:	n/a
47	chr4:110992869-110992919	Hela-S3	cervix:	n/a
48	chr4:110992869-110992919	HNPCEpiC	eye:	n/a
49	chr4:110992869-110992919	HRPEpiC	eye:	n/a
50	chr4:110992869-110992919	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:110989188..110991763-chr4:110992252..110995020,2	K562	blood:
2	chr4:110989188..110991763-chr4:110992252..110995020,2	K562	blood:

Variant related genes	Relation type
ELOVL6	TF binding region
ELOVL6	CpG island

Extended variants
information (count: 377 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569174936	chr4:110985404-110985405	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs183442445	chr4:110985427-110985428	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs13114826	chr4:110985432-110985433	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs34958560	chr4:110985520-110985521	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs573390441	chr4:110985592-110985593	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs188521941	chr4:110985676-110985677	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs376480513	chr4:110985680-110985681	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs552908225	chr4:110985681-110985682	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs572681742	chr4:110985720-110985721	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs542588276	chr4:110985721-110985722	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs114030827	chr4:110985733-110985734	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs192584983	chr4:110985736-110985737	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs185017930	chr4:110985751-110985752	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs563813831	chr4:110985775-110985776	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs529403581	chr4:110985810-110985811	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs549428529	chr4:110985923-110985924	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs566050163	chr4:110985924-110985925	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs372281833	chr4:110985937-110985938	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528393490	chr4:110985946-110985947	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs549815516	chr4:110986022-110986023	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs189400838	chr4:110986060-110986061	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs147214031	chr4:110986081-110986082	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs140753366	chr4:110986176-110986177	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs550356041	chr4:110986257-110986258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142269929	chr4:110986261-110986262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535926287	chr4:110986286-110986287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552708582	chr4:110986309-110986310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572768250	chr4:110986318-110986319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535009133	chr4:110986373-110986374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374177586	chr4:110986378-110986379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374716622	chr4:110986431-110986432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151235418	chr4:110986459-110986460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139310917	chr4:110986533-110986534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544076991	chr4:110986534-110986535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367793887	chr4:110986541-110986542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368989917	chr4:110986580-110986581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574221706	chr4:110986600-110986601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543073614	chr4:110986618-110986619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559511422	chr4:110986626-110986627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528442942	chr4:110986659-110986660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571372778	chr4:110986675-110986676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565228255	chr4:110986678-110986679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530690571	chr4:110986710-110986711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550393080	chr4:110986711-110986712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372100657	chr4:110986729-110986730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532203871	chr4:110986773-110986774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76982200	chr4:110986777-110986778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs17041326	chr4:110986845-110986846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs150000343	chr4:110986849-110986850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566354017	chr4:110986886-110986887	Weak transcription	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
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
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	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
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	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
Ovarian cancer	21720365	CNVD
Esophageal cancer	21851588	CNVD
Melanoma	20688739	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110964600-111004000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:110965200-110986600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:110965400-110994200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:110970800-110995800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr4:110971800-110992800	Weak transcription	Fetal Stomach	stomach
6	chr4:110973000-110991000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:110973000-111009200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr4:110973400-110992400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr4:110974400-110990600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr4:110974600-110992600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr4:110977200-110992400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr4:110977200-110992600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:110980200-110992600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr4:110980200-111004000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:110980800-110990800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr4:110981000-110997000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr4:110981000-111004200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:110981400-110991000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:110981400-110992600	Weak transcription	Adipose Nuclei	Adipose
20	chr4:110981400-111006200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:110981400-111009200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr4:110981600-110989400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:110982000-110988400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:110982000-110990600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:110982000-110991800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:110982000-110993200	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr4:110982000-110994400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr4:110982000-110994400	Weak transcription	Osteobl	bone
29	chr4:110982000-110995000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:110982000-110995800	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr4:110982000-111003800	Weak transcription	NHEK	skin
32	chr4:110982200-110994600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:110982600-110996200	Weak transcription	Dnd41	blood
34	chr4:110983600-110986000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr4:110983600-110988600	Weak transcription	K562	blood
36	chr4:110984000-110985600	Enhancers	Brain Cingulate Gyrus	brain
37	chr4:110984000-110985600	Enhancers	Brain Hippocampus Middle	brain
38	chr4:110984000-110998000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:110984000-111006200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:110984600-110986200	Enhancers	Liver	Liver
41	chr4:110984600-110992600	Weak transcription	Brain Substantia Nigra	brain
42	chr4:110984800-110990600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr4:110985000-110986200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr4:110985200-110985600	Enhancers	Fetal Intestine Small	intestine
45	chr4:110985200-110986800	Enhancers	HepG2	liver
46	chr4:110985400-110986000	Enhancers	Fetal Intestine Large	intestine
47	chr4:110985600-110986400	Weak transcription	Brain Cingulate Gyrus	brain
48	chr4:110985600-110990800	Weak transcription	Brain Hippocampus Middle	brain
49	chr4:110985600-111006000	Weak transcription	Fetal Intestine Small	intestine
50	chr4:110986000-110986200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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