Variant report

Variant	nsv870843
Chromosome Location	chr1:71465292-71489438
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	chr1:71468699-71468724	K562	blood:	n/a	n/a
2	ARID3A	chr1:71472265-71472284	K562	blood:	n/a	n/a
3	ARID3A	chr1:71481128-71481217	K562	blood:	n/a	n/a
4	BACH1	chr1:71468156-71468161	K562	blood:	n/a	n/a
5	BHLHE40	chr1:71465554-71465707	K562	blood:	n/a	n/a
6	BHLHE40	chr1:71485053-71485253	K562	blood:	n/a	n/a
7	BHLHE40	chr1:71480894-71480941	K562	blood:	n/a	n/a
8	CCNT2	chr1:71474825-71475012	K562	blood:	n/a	n/a
9	CEBPB	chr1:71485618-71485862	IMR90	lung:	n/a	chr1:71485756-71485767
10	CEBPB	chr1:71485706-71485857	A549	lung:	n/a	chr1:71485756-71485767
11	CEBPB	chr1:71470760-71470839	HepG2	liver:	n/a	chr1:71470810-71470821
12	CEBPB	chr1:71483442-71483555	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:71467360-71467695	K562	blood:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
14	CEBPB	chr1:71477312-71477504	HepG2	liver:	n/a	chr1:71477360-71477371
15	CEBPB	chr1:71477204-71477504	K562	blood:	n/a	chr1:71477360-71477371
16	CEBPB	chr1:71469996-71470196	K562	blood:	n/a	chr1:71470127-71470140 chr1:71470129-71470140
17	CEBPB	chr1:71467358-71467677	IMR90	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
18	CEBPB	chr1:71467389-71467679	H1-hESC	embryonic stem cell:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
19	CEBPB	chr1:71474287-71474494	K562	blood:	n/a	n/a
20	CEBPB	chr1:71467353-71467636	A549	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
21	CEBPB	chr1:71467330-71467690	HepG2	liver:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
22	CTCF	chr1:71478740-71478890	GM12866	blood:	n/a	n/a
23	CTCF	chr1:71467834-71467882	GM13977	blood:	n/a	n/a
24	CUX1	chr1:71481194-71481342	K562	blood:	n/a	n/a
25	CUX1	chr1:71466475-71466477	GM12878	blood:	n/a	n/a
26	EP300	chr1:71484933-71485359	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr1:71485426-71485674	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr1:71470322-71470837	ECC-1	luminal epithelium:	n/a	chr1:71470375-71470384
29	EP300	chr1:71484967-71485666	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr1:71484234-71487033	SK-N-SH	brain:	n/a	chr1:71486260-71486269 chr1:71484313-71484327 chr1:71484888-71484895 chr1:71485709-71485723
31	FOS	chr1:71483562-71483805	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:71483560-71483887	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:71481218-71481788	MCF10A-Er-Src	breast:	n/a	chr1:71481328-71481339
34	FOS	chr1:71481167-71481790	MCF10A-Er-Src	breast:	n/a	chr1:71481328-71481339
35	FOS	chr1:71481183-71481603	HUVEC	blood vessel:	n/a	chr1:71481328-71481339
36	FOS	chr1:71483560-71483868	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:71481207-71481680	MCF10A-Er-Src	breast:	n/a	chr1:71481328-71481339
38	FOS	chr1:71483558-71483802	MCF10A-Er-Src	breast:	n/a	n/a
39	FOXP2	chr1:71479770-71480138	SK-N-MC	brain:	n/a	n/a
40	GATA2	chr1:71484602-71485670	SH-SY5Y	brain:	n/a	chr1:71485136-71485145 chr1:71485611-71485620 chr1:71485610-71485620 chr1:71485503-71485513
41	GATA2	chr1:71464956-71465336	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr1:71464915-71465367	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr1:71484963-71486094	SH-SY5Y	brain:	n/a	chr1:71485136-71485145 chr1:71485611-71485620 chr1:71485610-71485620 chr1:71485503-71485513
44	GATA3	chr1:71473605-71473835	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr1:71479609-71480122	SK-N-SH	brain:	n/a	n/a
46	GATA3	chr1:71484932-71485641	SK-N-SH	brain:	n/a	chr1:71485136-71485145 chr1:71485611-71485620 chr1:71485610-71485620 chr1:71485503-71485513
47	GATA3	chr1:71484920-71485481	SK-N-SH	brain:	n/a	chr1:71485136-71485145
48	GATA3	chr1:71479599-71480290	SK-N-SH	brain:	n/a	n/a
49	JUN	chr1:71478258-71478560	K562	blood:	n/a	n/a
50	JUN	chr1:71465696-71465994	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71472738-71472788	HRCEpiC	kidney:	n/a
2	chr1:71472738-71472788	GM19239	blood:	n/a
3	chr1:71472738-71472788	HL-60	blood:	n/a
4	chr1:71472738-71472788	Jurkat	blood:	n/a
5	chr1:71472738-71472788	BJ	skin:	n/a
6	chr1:71472738-71472788	H1-hESC	embryonic stem cell:	embryo
7	chr1:71472738-71472788	MCF10A-Er-Src	breast:	n/a
8	chr1:71472738-71472788	U87	brain:	n/a
9	chr1:71472738-71472788	Caco-2	colon:	n/a
10	chr1:71472738-71472788	AoSMC	blood vessel:	n/a
11	chr1:71472738-71472788	GM12878	blood:	n/a
12	chr1:71472738-71472788	MCF-7	breast:	n/a
13	chr1:71472738-71472788	ECC-1	luminal epithelium:	n/a
14	chr1:71472738-71472788	IMR90	lung:	fetal
15	chr1:71472738-71472788	GM12892	blood:	n/a
16	chr1:71472738-71472788	SK-N-SH	brain:	n/a
17	chr1:71472738-71472788	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:71472738-71472788	Hepatocyte	liver:	n/a
19	chr1:71472738-71472788	NB4	blood:	n/a
20	chr1:71472738-71472788	HCM	heart:	n/a
21	chr1:71472738-71472788	ProgFib	skin:	n/a
22	chr1:71472738-71472788	SK-N-MC	brain:	n/a
23	chr1:71472738-71472788	HIPEpiC	eye:	n/a
24	chr1:71472738-71472788	GM12891	blood:	n/a
25	chr1:71472738-71472788	HMEC	breast:	n/a
26	chr1:71472738-71472788	NT2-D1	testis:	n/a
27	chr1:71472738-71472788	HUVEC	blood vessel:	n/a
28	chr1:71472738-71472788	HAEpiC	amniotic membrane:	n/a
29	chr1:71472738-71472788	PFSK-1	brain:	n/a
30	chr1:71472738-71472788	HCPEpiC	choroid plexus:	n/a
31	chr1:71472738-71472788	HCF	heart:	n/a
32	chr1:71472738-71472788	LNCaP	prostate:	n/a
33	chr1:71472738-71472788	AG09309	skin:	n/a
34	chr1:71472738-71472788	PrEC	prostate:	n/a
35	chr1:71472738-71472788	HRPEpiC	eye:	n/a
36	chr1:71472738-71472788	AG10803	skin:	n/a
37	chr1:71472738-71472788	CMK	blood:	n/a
38	chr1:71472738-71472788	SAEC	small airway:	n/a
39	chr1:71472738-71472788	BE2_C	brain:	n/a
40	chr1:71472738-71472788	A549	lung:	n/a
41	chr1:71472738-71472788	NHBE	bronchial:	n/a
42	chr1:71472738-71472788	HEEpiC	esophagus:	n/a
43	chr1:71472738-71472788	AG09319	gingival:	n/a
44	chr1:71472738-71472788	HepG2	liver:	n/a
45	chr1:71472738-71472788	NH-A	brain:	n/a
46	chr1:71472738-71472788	HEK293	kidney:	embryo
47	chr1:71472738-71472788	SK-N-SH_RA	brain:	n/a
48	chr1:71472738-71472788	GM06990	blood:	n/a
49	chr1:71472738-71472788	SKMC	muscle:	n/a
50	chr1:71472738-71472788	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:71486485..71490048-chr1:71491402..71493576,3	K562	blood:
2	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
3	chr1:71488156..71490050-chr1:71494544..71497230,2	K562	blood:
4	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
5	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
6	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
7	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
8	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
9	chr1:71488605..71491550-chr1:71545533..71547496,2	K562	blood:
10	chr1:71467023..71468927-chr1:71512007..71514052,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-13	chr1:71489270-71489329	NONHSAT003876
2	lnc-ZRANB2-3	chr1:71471537-71472185	ENSG00000269933.1
3	lnc-CTH-14	chr1:71475401-71475924	l_71_chr1:71319635-71475982_testes
4	lnc-CTH-14	chr1:71475926-71475982	l_71_chr1:71319635-71475982_testes
5	lnc-ZRANB2-2	chr1:71472542-71473814	NONHSAT003875

Variant related genes	Relation type
ENSG00000269933	TF binding region
ENSG00000269933	CpG island
ENSG00000132485	chromatin interactions
ENSG00000050628	chromatin interactions
ENSG00000229956	chromatin interactions

Extended variants
information (count: 830 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:830 , 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	rs2268055	chr1:71465292-71465293	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574846211	chr1:71465334-71465335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148663161	chr1:71465351-71465352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2744912	chr1:71465398-71465399	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs577361470	chr1:71465454-71465455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546513202	chr1:71465481-71465482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553664417	chr1:71465501-71465502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573463446	chr1:71465508-71465509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142234807	chr1:71465529-71465530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151217746	chr1:71465583-71465584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530613252	chr1:71465607-71465608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs36084336	chr1:71465615-71465616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368149085	chr1:71465652-71465653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370212731	chr1:71465690-71465691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140365699	chr1:71465775-71465776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189192221	chr1:71465784-71465785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546197013	chr1:71465856-71465857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145368308	chr1:71465860-71465861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180888633	chr1:71465891-71465892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570517791	chr1:71465924-71465925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533924691	chr1:71465943-71465944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186493976	chr1:71465978-71465979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190153555	chr1:71466038-71466039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568989175	chr1:71466048-71466049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537553339	chr1:71466087-71466088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370114812	chr1:71466101-71466102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373861963	chr1:71466138-71466139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570969389	chr1:71466205-71466206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181162544	chr1:71466302-71466303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559144451	chr1:71466347-71466348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369592562	chr1:71466372-71466373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553426410	chr1:71466405-71466406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573450653	chr1:71466406-71466407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542194309	chr1:71466560-71466561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11209732	chr1:71466633-71466634	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs10789315	chr1:71466644-71466645	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs147655382	chr1:71466658-71466659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563797032	chr1:71466701-71466702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563592191	chr1:71466714-71466715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532865258	chr1:71466723-71466724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186153444	chr1:71466724-71466725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142444080	chr1:71466793-71466794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529168669	chr1:71466815-71466816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138831761	chr1:71466879-71466880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376986732	chr1:71466881-71466882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28548948	chr1:71466905-71466906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115895239	chr1:71466919-71466920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554204284	chr1:71466931-71466932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532658601	chr1:71466951-71466952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569027480	chr1:71467063-71467064	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71461800-71465600	Weak transcription	K562	blood
2	chr1:71465000-71465600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:71465000-71466000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr1:71465200-71465600	Enhancers	Primary hematopoietic stem cells	blood
5	chr1:71465200-71465600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:71465200-71467400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:71465400-71465800	Enhancers	Pancreas	Pancrea
8	chr1:71465600-71466000	Enhancers	K562	blood
9	chr1:71465800-71485000	Weak transcription	Pancreas	Pancrea
10	chr1:71466000-71467000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr1:71466000-71475200	Weak transcription	K562	blood
12	chr1:71467000-71467200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr1:71467400-71469600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:71467800-71475400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:71468400-71472800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:71469600-71469800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:71469800-71470200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:71470200-71470800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:71470400-71470600	Enhancers	Adipose Nuclei	Adipose
20	chr1:71470400-71470800	Enhancers	Placenta	Placenta
21	chr1:71470600-71477600	Weak transcription	Adipose Nuclei	Adipose
22	chr1:71472800-71474000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:71473600-71478000	Weak transcription	Aorta	Aorta
24	chr1:71474000-71474600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:71474600-71478200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:71475200-71476200	Strong transcription	K562	blood
27	chr1:71475400-71478200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:71476200-71477200	Weak transcription	K562	blood
29	chr1:71477200-71478600	Strong transcription	K562	blood
30	chr1:71477600-71478200	Strong transcription	Adipose Nuclei	Adipose
31	chr1:71477800-71478200	Enhancers	Fetal Stomach	stomach
32	chr1:71478000-71478200	Enhancers	Aorta	Aorta
33	chr1:71478200-71479600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:71478200-71479600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:71478200-71482600	Weak transcription	Aorta	Aorta
36	chr1:71478200-71483200	Weak transcription	Adipose Nuclei	Adipose
37	chr1:71478600-71480400	Weak transcription	K562	blood
38	chr1:71479600-71481600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:71479600-71482000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:71479800-71480600	Enhancers	Fetal Heart	heart
41	chr1:71480400-71481800	Enhancers	K562	blood
42	chr1:71480600-71484400	Weak transcription	Fetal Heart	heart
43	chr1:71481600-71482800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:71481800-71501000	Weak transcription	K562	blood
45	chr1:71482000-71483400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:71482600-71483800	Enhancers	Aorta	Aorta
47	chr1:71482800-71484000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:71483000-71483800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:71483000-71483800	Enhancers	Placenta	Placenta
50	chr1:71483200-71483600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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