Variant report

Variant	esv3374788
Chromosome Location	chr10:45419346-45423644
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	ATF1	chr10:45420744-45421360	K562	blood:	n/a	n/a
2	ATF2	chr10:45420618-45421003	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr10:45421231-45421726	GM12878	blood:	n/a	n/a
4	BCL3	chr10:45421140-45421796	GM12878	blood:	n/a	n/a
5	BRCA1	chr10:45420864-45420880	HepG2	liver:	n/a	n/a
6	CEBPB	chr10:45422640-45422985	IMR90	lung:	n/a	chr10:45422822-45422833
7	CEBPB	chr10:45422643-45423015	HepG2	liver:	n/a	chr10:45422822-45422833
8	CEBPB	chr10:45422631-45423079	HepG2	liver:	n/a	chr10:45422822-45422833
9	CEBPB	chr10:45420648-45421013	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr10:45422701-45422923	HepG2	liver:	n/a	chr10:45422822-45422833
11	CEBPB	chr10:45422676-45422897	Hela-S3	cervix:	n/a	chr10:45422822-45422833
12	CEBPB	chr10:45420745-45420962	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:45422676-45422951	K562	blood:	n/a	chr10:45422822-45422833
14	CHD2	chr10:45420209-45420256	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr10:45420632-45421043	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr10:45421322-45421509	GM12878	blood:	n/a	n/a
17	CREB1	chr10:45420628-45421094	H1-hESC	embryonic stem cell:	n/a	chr10:45420852-45420865
18	CTCF	chr10:45420720-45420870	HEK293	kidney:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
19	CTCF	chr10:45420160-45420310	HRPEpiC	eye:	n/a	chr10:45420266-45420282
20	CTCF	chr10:45420700-45420850	HEK293	kidney:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
21	CTCF	chr10:45420710-45420959	MCF-7	breast:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
22	CTCF	chr10:45420636-45421013	GM12878	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
23	CTCF	chr10:45420715-45420968	GM19238	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
24	CTCF	chr10:45420700-45420850	GM12867	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
25	CTCF	chr10:45420680-45420830	GM12864	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
26	CTCF	chr10:45420660-45420810	HMF	breast:	n/a	n/a
27	CTCF	chr10:45420700-45420850	GM12864	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
28	CTCF	chr10:45420720-45420870	AG04449	skin:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
29	CTCF	chr10:45420743-45420877	LNCaP	prostate:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
30	CTCF	chr10:45420718-45420941	MCF-7	breast:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
31	CTCF	chr10:45420700-45420850	HPF	lung:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
32	CTCF	chr10:45420734-45420936	Gliobla	brain:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
33	CTCF	chr10:45420631-45421031	K562	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
34	CTCF	chr10:45420714-45420939	MCF-7	breast:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
35	CTCF	chr10:45420820-45420970	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr10:45420708-45420714	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr10:45420680-45420830	GM12873	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
38	CTCF	chr10:45420720-45420870	BJ	skin:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
39	CTCF	chr10:45420700-45420850	HCT-116	colon:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
40	CTCF	chr10:45420720-45420870	GM12865	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
41	CTCF	chr10:45420711-45420892	A549	lung:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
42	CTCF	chr10:45420720-45420870	HCM	heart:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
43	CTCF	chr10:45420689-45420938	MCF-7	breast:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
44	CTCF	chr10:45420760-45420910	NB4	blood:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
45	CTCF	chr10:45420760-45420910	WERI-Rb-1	eye:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
46	CTCF	chr10:45420780-45420930	A549	lung:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
47	CTCF	chr10:45420800-45420950	HFF	foreskin:	n/a	chr10:45420806-45420819 chr10:45420804-45420822
48	CTCF	chr10:45420586-45421008	H1-hESC	embryonic stem cell:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822
49	CTCF	chr10:45420820-45420970	K562	blood:	n/a	n/a
50	CTCF	chr10:45420700-45420850	HCFaa	heart:	n/a	chr10:45420806-45420819 chr10:45420799-45420820 chr10:45420804-45420822

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:45420821-45420871	SK-N-SH_RA	brain:	n/a
2	chr10:45420821-45420871	MCF-7	breast:	n/a
3	chr10:45420821-45420871	GM12878	blood:	n/a
4	chr10:45420821-45420871	HMEC	breast:	n/a
5	chr10:45420821-45420871	HRCEpiC	kidney:	n/a
6	chr10:45420821-45420871	PFSK-1	brain:	n/a
7	chr10:45420821-45420871	NHBE	bronchial:	n/a
8	chr10:45420821-45420871	GM12891	blood:	n/a
9	chr10:45420821-45420871	HNPCEpiC	eye:	n/a
10	chr10:45420821-45420871	NB4	blood:	n/a
11	chr10:45420821-45420871	ProgFib	skin:	n/a
12	chr10:45420821-45420871	HEEpiC	esophagus:	n/a
13	chr10:45420821-45420871	Hepatocyte	liver:	n/a
14	chr10:45420821-45420871	HCPEpiC	choroid plexus:	n/a
15	chr10:45420821-45420871	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:45420821-45420871	BE2_C	brain:	n/a
17	chr10:45420821-45420871	LNCaP	prostate:	n/a
18	chr10:45420821-45420871	CMK	blood:	n/a
19	chr10:45420821-45420871	HRPEpiC	eye:	n/a
20	chr10:45420821-45420871	Hela-S3	cervix:	n/a
21	chr10:45420821-45420871	HCT-116	colon:	n/a
22	chr10:45420821-45420871	SK-N-MC	brain:	n/a
23	chr10:45420821-45420871	K562	blood:	n/a
24	chr10:45420821-45420871	MCF10A-Er-Src	breast:	n/a
25	chr10:45420821-45420871	HL-60	blood:	n/a
26	chr10:45420821-45420871	AG10803	skin:	n/a
27	chr10:45420821-45420871	IMR90	lung:	fetal
28	chr10:45420821-45420871	AoSMC	blood vessel:	n/a
29	chr10:45420821-45420871	PANC-1	pancreas:	n/a
30	chr10:45420821-45420871	AG09319	gingival:	n/a
31	chr10:45420821-45420871	GM12892	blood:	n/a
32	chr10:45420821-45420871	SAEC	small airway:	n/a
33	chr10:45420821-45420871	AG04449	skin:	fetal
34	chr10:45420821-45420871	HIPEpiC	eye:	n/a
35	chr10:45420821-45420871	ovcar-3	ovarian:	n/a
36	chr10:45420821-45420871	NT2-D1	testis:	n/a
37	chr10:45420821-45420871	BJ	skin:	n/a
38	chr10:45420821-45420871	Jurkat	blood:	n/a
39	chr10:45420821-45420871	ECC-1	luminal epithelium:	n/a
40	chr10:45420821-45420871	HepG2	liver:	n/a
41	chr10:45420821-45420871	H1-hESC	embryonic stem cell:	embryo
42	chr10:45420821-45420871	U87	brain:	n/a
43	chr10:45420821-45420871	GM06990	blood:	n/a
44	chr10:45420821-45420871	AG04450	lung:	fetal
45	chr10:45420821-45420871	SKMC	muscle:	n/a
46	chr10:45420821-45420871	HAEpiC	amniotic membrane:	n/a
47	chr10:45420821-45420871	HCF	heart:	n/a
48	chr10:45420821-45420871	HUVEC	blood vessel:	n/a
49	chr10:45420821-45420871	HRE	kidney:	n/a
50	chr10:45420821-45420871	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:45419232..45422212-chr10:45424408..45426713,2	K562	blood:
2	chr10:45358763..45359359-chr10:45420588..45421166,2	MCF-7	breast:
3	chr10:45359809..45360961-chr10:45420280..45421173,6	MCF-7	breast:
4	chr10:45423081..45426439-chr10:45487238..45490931,4	K562	blood:
5	chr10:45406644..45408622-chr10:45422950..45424971,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASSF4-2	chr10:45420766-45420801	NONHSAT013045

Variant related genes	Relation type
ENSG00000234504	TF binding region
TMEM72	TF binding region
ENSG00000234504	CpG island
TMEM72	CpG island
ENSG00000187783	chromatin interactions

Extended variants
information (count: 207 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:207 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559899342	chr10:45419385-45419386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150991526	chr10:45419387-45419388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550931602	chr10:45419425-45419426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186942275	chr10:45419486-45419487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529916530	chr10:45419569-45419570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548226781	chr10:45419577-45419578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76018888	chr10:45419602-45419603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533754027	chr10:45419626-45419627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558246921	chr10:45419628-45419629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570148612	chr10:45419635-45419636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538142015	chr10:45419656-45419657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556487110	chr10:45419665-45419666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574647970	chr10:45419707-45419708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370536677	chr10:45419714-45419715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7477198	chr10:45419744-45419745	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs554207156	chr10:45419756-45419757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572471465	chr10:45419816-45419817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548678513	chr10:45419824-45419825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551552056	chr10:45419875-45419876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564310632	chr10:45419906-45419907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576551313	chr10:45419919-45419920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570063551	chr10:45419926-45419927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544469043	chr10:45419942-45419943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562778800	chr10:45419953-45419954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529879846	chr10:45419954-45419955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548106406	chr10:45419955-45419956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560322827	chr10:45419961-45419962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192244894	chr10:45419962-45419963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs5784658	chr10:45419974-45419975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527380770	chr10:45419978-45419979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1332623	chr10:45419998-45419999	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs34634089	chr10:45420052-45420053	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs533576978	chr10:45420053-45420054	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs35814342	chr10:45420055-45420056	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs570111444	chr10:45420065-45420066	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs139298756	chr10:45420070-45420071	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs1332622	chr10:45420076-45420077	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs568432195	chr10:45420139-45420140	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs536022255	chr10:45420156-45420157	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs371726870	chr10:45420158-45420159	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs570801009	chr10:45420204-45420205	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs554054099	chr10:45420227-45420228	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs145493651	chr10:45420269-45420270	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs147667184	chr10:45420270-45420271	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs539654618	chr10:45420284-45420285	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183371025	chr10:45420293-45420294	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs576463424	chr10:45420298-45420299	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs543853007	chr10:45420312-45420313	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs375719707	chr10:45420377-45420378	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs76079074	chr10:45420415-45420416	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Glioblastoma multiforme	21138945	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45407800-45422800	Weak transcription	Ovary	ovary
2	chr10:45410200-45430400	Weak transcription	Gastric	stomach
3	chr10:45410600-45419600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:45413200-45420400	Weak transcription	Fetal Kidney	kidney
5	chr10:45413400-45428200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr10:45415400-45420000	Weak transcription	HSMMtube	muscle
7	chr10:45416200-45419800	Weak transcription	Fetal Muscle Leg	muscle
8	chr10:45417000-45434000	Weak transcription	Fetal Brain Female	brain
9	chr10:45417800-45422400	Weak transcription	Duodenum Mucosa	Duodenum
10	chr10:45418800-45420800	Weak transcription	Spleen	Spleen
11	chr10:45418800-45424800	Weak transcription	Colonic Mucosa	Colon
12	chr10:45419200-45420200	Weak transcription	Lung	lung
13	chr10:45419200-45420200	Weak transcription	Pancreas	Pancrea
14	chr10:45419400-45420800	Enhancers	Fetal Thymus	thymus
15	chr10:45419600-45420400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr10:45419600-45421000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr10:45419800-45420600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr10:45419800-45421000	Enhancers	Fetal Muscle Trunk	muscle
19	chr10:45419800-45421200	Enhancers	Fetal Muscle Leg	muscle
20	chr10:45420000-45420200	Bivalent Enhancer	HepG2	liver
21	chr10:45420000-45420400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr10:45420000-45421200	Enhancers	HSMMtube	muscle
23	chr10:45420200-45420400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:45420200-45420800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr10:45420200-45421000	Enhancers	Lung	lung
26	chr10:45420200-45421000	Enhancers	Pancreas	Pancrea
27	chr10:45420200-45422200	Enhancers	HepG2	liver
28	chr10:45420400-45420600	Enhancers	Fetal Lung	lung
29	chr10:45420400-45420800	Enhancers	Fetal Kidney	kidney
30	chr10:45420400-45421000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr10:45420400-45428000	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr10:45420400-45428200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:45420600-45421000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr10:45420600-45421600	Bivalent Enhancer	K562	blood
35	chr10:45420800-45421000	Enhancers	Right Ventricle	heart
36	chr10:45420800-45421000	Enhancers	Spleen	Spleen
37	chr10:45420800-45421200	Weak transcription	Fetal Kidney	kidney
38	chr10:45420800-45422800	Weak transcription	Fetal Thymus	thymus
39	chr10:45421000-45421400	Enhancers	Fetal Heart	heart
40	chr10:45421000-45421600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr10:45421000-45421600	Weak transcription	Spleen	Spleen
42	chr10:45421000-45422400	Weak transcription	Pancreas	Pancrea
43	chr10:45421000-45422800	Weak transcription	Fetal Muscle Trunk	muscle
44	chr10:45421000-45423200	Weak transcription	Lung	lung
45	chr10:45421000-45427800	Weak transcription	Right Ventricle	heart
46	chr10:45421200-45421800	ZNF genes & repeats	Fetal Kidney	kidney
47	chr10:45421200-45422200	Weak transcription	HSMMtube	muscle
48	chr10:45421200-45422400	Weak transcription	Fetal Muscle Leg	muscle
49	chr10:45421400-45421600	Genic enhancers	Fetal Heart	heart
50	chr10:45421600-45421800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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