Variant report

Variant	nsv1060684
Chromosome Location	chr22:34108462-34140653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:64)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr22:34135101-34135251	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr22:34139772-34140140	GM12878	blood:	n/a	n/a
3	BHLHE40	chr22:34119934-34120194	GM12878	blood:	n/a	n/a
4	BHLHE40	chr22:34114028-34114321	HepG2	liver:	n/a	n/a
5	CTCF	chr22:34122620-34122770	AoAF	blood vessel:	n/a	n/a
6	CTCF	chr22:34118840-34118900	GM13976	blood:	n/a	n/a
7	CTCF	chr22:34122620-34122770	AG04450	lung:	n/a	n/a
8	CTCF	chr22:34122600-34122750	HPF	lung:	n/a	n/a
9	CTCF	chr22:34112658-34112721	GM10248	blood:	n/a	n/a
10	CTCF	chr22:34122620-34122770	HEK293	kidney:	n/a	n/a
11	CTCF	chr22:34122660-34122810	NHLF	lung:	n/a	n/a
12	CTCF	chr22:34122700-34122850	HepG2	liver:	n/a	n/a
13	CTCF	chr22:34133324-34133341	GM10266	blood:	n/a	n/a
14	ELF1	chr22:34119930-34120284	GM12878	blood:	n/a	n/a
15	FOXA1	chr22:34113968-34114382	HepG2	liver:	n/a	n/a
16	FOXA1	chr22:34113914-34114289	HepG2	liver:	n/a	n/a
17	FOXA1	chr22:34116363-34116773	HepG2	liver:	n/a	n/a
18	FOXA1	chr22:34114008-34114341	HepG2	liver:	n/a	n/a
19	FOXA1	chr22:34113934-34114371	HepG2	liver:	n/a	n/a
20	FOXA1	chr22:34116395-34116822	HepG2	liver:	n/a	n/a
21	FOXA1	chr22:34116500-34116908	HepG2	liver:	n/a	n/a
22	FOXA1	chr22:34116402-34116904	HepG2	liver:	n/a	n/a
23	FOXA2	chr22:34116556-34116801	HepG2	liver:	n/a	n/a
24	FOXA2	chr22:34113986-34114341	HepG2	liver:	n/a	n/a
25	GATA2	chr22:34125601-34125945	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr22:34123270-34123541	SH-SY5Y	brain:	n/a	n/a
27	HNF4A	chr22:34116503-34116815	HepG2	liver:	n/a	chr22:34116628-34116643 chr22:34116637-34116645
28	HNF4A	chr22:34116433-34116733	HepG2	liver:	n/a	chr22:34116628-34116643 chr22:34116637-34116645
29	JUN	chr22:34130194-34130203	HepG2	liver:	n/a	n/a
30	JUND	chr22:34130090-34130220	HepG2	liver:	n/a	n/a
31	KAP1	chr22:34139070-34139349	HEK293	kidney:	n/a	n/a
32	MAFF	chr22:34124873-34125218	HepG2	liver:	n/a	chr22:34125184-34125198
33	MAFK	chr22:34127721-34127852	HepG2	liver:	n/a	n/a
34	MAFK	chr22:34124966-34125073	K562	blood:	n/a	n/a
35	MAFK	chr22:34124864-34125214	HepG2	liver:	n/a	chr22:34125181-34125201 chr22:34125184-34125198 chr22:34125183-34125199
36	MAFK	chr22:34124877-34125213	IMR90	lung:	n/a	chr22:34125181-34125201 chr22:34125184-34125198 chr22:34125183-34125199
37	MAFK	chr22:34124878-34125296	HepG2	liver:	n/a	chr22:34125181-34125201 chr22:34125184-34125198 chr22:34125183-34125199
38	MAX	chr22:34134351-34134551	H1-hESC	embryonic stem cell:	n/a	chr22:34134464-34134474
39	MAX	chr22:34119844-34120284	NB4	blood:	n/a	n/a
40	MYC	chr22:34119881-34120270	NB4	blood:	n/a	n/a
41	MYC	chr22:34125971-34126004	MCF-7	breast:	n/a	n/a
42	NANOG	chr22:34134140-34134477	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr22:34136070-34136210	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr22:34128411-34128496	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr22:34128815-34129100	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr22:34133720-34134108	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr22:34139355-34139411	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr22:34118438-34118513	HepG2	liver:	n/a	n/a
49	POLR2A	chr22:34136929-34137288	H1-neurons	neurons:	n/a	n/a
50	POLR2A	chr22:34129354-34129569	GM12878	blood:	n/a	n/a

No data

(count:64 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIMP3-6	chr22:34121026-34121087	ENSG00000224973.1
2	lnc-TIMP3-6	chr22:34120972-34121087	NONHSAT085012
3	lnc-TIMP3-6	chr22:34128242-34129671	ENSG00000224973.1
4	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085011
5	lnc-TIMP3-6	chr22:34121000-34121087	NONHSAT085013
6	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085013
7	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
8	lnc-TIMP3-6	chr22:34140116-34140179	ENSG00000224973.1
9	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085018
10	lnc-TIMP3-6	chr22:34139122-34139185	ENSG00000224973.1
11	lnc-TIMP3-6	chr22:34121003-34121087	NONHSAT085015
12	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
13	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1
14	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085015
15	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085015
16	lnc-TIMP3-6	chr22:34133550-34133761	ENSG00000224973.1
17	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085013
18	lnc-TIMP3-6	chr22:34121055-34121087	ENSG00000224973.1
19	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085013
20	lnc-TIMP3-6	chr22:34123477-34123574	NONHSAT085013
21	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085012
22	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
23	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085012
24	lnc-TIMP3-6	chr22:34139996-34140315	ENSG00000224973.1
25	lnc-TIMP3-6	chr22:34133550-34133769	ENSG00000224973.1
26	lnc-TIMP3-6	chr22:34121058-34121087	ENSG00000224973.1
27	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
28	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085011
29	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085014
30	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1
31	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085014
32	lnc-SYN3-4	chr22:34119818-34120265	ENSG00000232081.1
33	lnc-TIMP3-6	chr22:34133550-34133769	ENSG00000224973.1
34	lnc-TIMP3-6	chr22:34128242-34128488	ENSG00000224973.1
35	lnc-SYN3-4	chr22:34120789-34120898	ENSG00000232081.1
36	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
37	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
38	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
39	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085012
40	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085013
41	lnc-TIMP3-6	chr22:34121000-34121087	ENSG00000224973.1
42	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085015
43	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085011
44	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085011
45	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
46	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085014
47	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
48	lnc-TIMP3-6	chr22:34128267-34128635	NONHSAT085018
49	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085011
50	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1

No data

Variant related genes	Relation type
LARGE-AS1	TF binding region
LARGE-IT1	TF binding region

Extended variants
information (count: 1429 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5999068	chr22:34108462-34108463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs9621757	chr22:34108484-34108485	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs562705961	chr22:34108486-34108487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537290803	chr22:34108489-34108490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531513203	chr22:34108499-34108500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551501521	chr22:34108505-34108506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368339525	chr22:34108513-34108514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527340186	chr22:34108523-34108524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565353455	chr22:34108561-34108562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547084155	chr22:34108584-34108585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375810974	chr22:34108624-34108625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576097430	chr22:34108628-34108629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34754283	chr22:34108662-34108663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566896453	chr22:34108702-34108703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536566676	chr22:34108711-34108712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556427235	chr22:34108735-34108736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569960620	chr22:34108763-34108764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538845039	chr22:34108781-34108782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs16992842	chr22:34108835-34108836	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs9621758	chr22:34108851-34108852	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571828278	chr22:34108865-34108866	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572450833	chr22:34108872-34108873	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs16992847	chr22:34108887-34108888	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185374643	chr22:34108909-34108910	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190319087	chr22:34108918-34108919	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574869263	chr22:34108928-34108929	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542972374	chr22:34108955-34108956	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4821176	chr22:34109005-34109006	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs531577122	chr22:34109060-34109061	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535188585	chr22:34109072-34109073	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142054831	chr22:34109082-34109083	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527420327	chr22:34109085-34109086	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151177771	chr22:34109096-34109097	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542225089	chr22:34109131-34109132	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566960070	chr22:34109149-34109150	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552910342	chr22:34109163-34109164	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181514750	chr22:34109168-34109169	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570020482	chr22:34109173-34109174	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76114213	chr22:34109215-34109216	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185826202	chr22:34109236-34109237	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111794112	chr22:34109237-34109238	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4821177	chr22:34109309-34109310	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs59984379	chr22:34109345-34109346	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188580571	chr22:34109347-34109348	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574934631	chr22:34109348-34109349	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543616250	chr22:34109361-34109362	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543831041	chr22:34109362-34109363	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181055689	chr22:34109383-34109384	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557351414	chr22:34109415-34109416	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563792264	chr22:34109451-34109452	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34087000-34109400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr22:34091600-34115800	Weak transcription	Pancreas	Pancrea
3	chr22:34092400-34109200	Weak transcription	Fetal Intestine Large	intestine
4	chr22:34097000-34110000	Weak transcription	Ovary	ovary
5	chr22:34097200-34109200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr22:34097200-34109200	Weak transcription	Fetal Brain Female	brain
7	chr22:34097200-34109400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr22:34097600-34110200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr22:34097600-34114600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr22:34098200-34110600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr22:34100400-34109000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr22:34100800-34110000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr22:34101200-34108800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr22:34101200-34109600	Weak transcription	Fetal Stomach	stomach
15	chr22:34101200-34110000	Weak transcription	Aorta	Aorta
16	chr22:34103200-34110600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr22:34104000-34110000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr22:34104200-34118800	Weak transcription	Right Ventricle	heart
19	chr22:34104600-34109400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr22:34105000-34109800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr22:34105200-34109800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr22:34105600-34133400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr22:34106400-34110200	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr22:34106600-34109200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr22:34106600-34109400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr22:34106600-34109400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr22:34106600-34109400	Weak transcription	Brain Hippocampus Middle	brain
28	chr22:34106600-34110000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr22:34107200-34109800	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr22:34107200-34110000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr22:34107200-34110000	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr22:34107600-34111400	Weak transcription	Left Ventricle	heart
33	chr22:34107600-34116200	Weak transcription	Stomach Mucosa	stomach
34	chr22:34108200-34109200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr22:34108400-34109200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr22:34108400-34109400	Enhancers	HepG2	liver
37	chr22:34108800-34109800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr22:34109000-34110000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr22:34109200-34109400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr22:34109200-34109800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
41	chr22:34109400-34109800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr22:34109400-34109800	Weak transcription	Liver	Liver
43	chr22:34109400-34110400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr22:34109400-34110800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr22:34109400-34112000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
46	chr22:34109400-34112400	Weak transcription	HepG2	liver
47	chr22:34109600-34111000	ZNF genes & repeats	Fetal Stomach	stomach
48	chr22:34109800-34110800	ZNF genes & repeats	Liver	Liver
49	chr22:34109800-34111000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
50	chr22:34109800-34111200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived

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