Variant report

Variant	esv3449576
Chromosome Location	chr10:94048622-94050670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:593)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94050518-94051175	HepG2	liver:	n/a	n/a
2	ATF1	chr10:94050664-94051066	K562	blood:	n/a	n/a
3	ATF2	chr10:94050558-94050955	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:94050518-94051044	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr10:94050647-94051174	GM12878	blood:	n/a	n/a
6	ATF2	chr10:94050622-94051094	GM12878	blood:	n/a	n/a
7	ATF3	chr10:94050625-94051037	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:94050152-94050836	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr10:94050505-94051165	A549	lung:	n/a	chr10:94050797-94050806 chr10:94050585-94050592 chr10:94051091-94051104 chr10:94051090-94051099
10	BCLAF1	chr10:94050526-94051303	GM12878	blood:	n/a	chr10:94050797-94050806 chr10:94050585-94050592 chr10:94051091-94051104 chr10:94051090-94051099
11	BCLAF1	chr10:94050183-94051237	GM12878	blood:	n/a	chr10:94050797-94050806 chr10:94050585-94050592 chr10:94051091-94051104 chr10:94051090-94051099
12	BHLHE40	chr10:94050075-94051066	K562	blood:	n/a	n/a
13	BHLHE40	chr10:94050053-94051141	GM12878	blood:	n/a	n/a
14	BRCA1	chr10:94050637-94051279	HepG2	liver:	n/a	n/a
15	BRCA1	chr10:94050649-94051233	GM12878	blood:	n/a	n/a
16	BRCA1	chr10:94050658-94050934	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr10:94049868-94050296	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr10:94050589-94051137	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr10:94050556-94051245	K562	blood:	n/a	n/a
20	CCNT2	chr10:94050550-94051437	K562	blood:	n/a	chr10:94050608-94050617 chr10:94050572-94050581
21	CCNT2	chr10:94049994-94050259	K562	blood:	n/a	chr10:94050098-94050107
22	CEBPB	chr10:94050363-94051105	IMR90	lung:	n/a	n/a
23	CEBPB	chr10:94050612-94051108	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr10:94050416-94051097	A549	lung:	n/a	n/a
25	CEBPB	chr10:94049922-94051138	Hela-S3	cervix:	n/a	n/a
26	CEBPD	chr10:94050469-94050881	HepG2	liver:	n/a	n/a
27	CHD1	chr10:94050412-94051261	GM12878	blood:	n/a	n/a
28	CHD2	chr10:94050219-94051094	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr10:94049874-94051517	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr10:94050022-94051602	GM12878	blood:	n/a	n/a
31	CHD2	chr10:94050578-94050848	K562	blood:	n/a	n/a
32	CREB1	chr10:94049883-94051564	HepG2	liver:	n/a	n/a
33	CREB1	chr10:94050274-94051299	GM12878	blood:	n/a	n/a
34	CREB1	chr10:94050276-94051348	GM12878	blood:	n/a	n/a
35	CREB1	chr10:94050572-94051278	ECC-1	luminal epithelium:	n/a	n/a
36	CREB1	chr10:94050572-94051239	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr10:94050439-94051433	K562	blood:	n/a	n/a
38	CREB1	chr10:94050520-94051349	K562	blood:	n/a	n/a
39	CREB1	chr10:94050567-94051132	ECC-1	luminal epithelium:	n/a	n/a
40	CREB1	chr10:94050552-94051267	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr10:94050538-94051293	A549	lung:	n/a	n/a
42	CREB1	chr10:94050496-94051290	HepG2	liver:	n/a	n/a
43	CTBP2	chr10:94049938-94051525	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr10:94050020-94050170	GM12872	blood:	n/a	n/a
45	CTCF	chr10:94050280-94050430	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr10:94050400-94050550	HMF	breast:	n/a	n/a
47	CTCF	chr10:94050660-94050810	HFF	foreskin:	n/a	chr10:94050753-94050762
48	CTCF	chr10:94050660-94050810	MCF-7	breast:	n/a	chr10:94050753-94050762
49	CTCF	chr10:94050640-94050790	HCM	heart:	n/a	chr10:94050753-94050762
50	CTCF	chr10:94050640-94050790	HL-60	blood:	n/a	chr10:94050753-94050762

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94050649-94050699	HEK293	kidney:	embryo
2	chr10:94050516-94050566	HUVEC	blood vessel:	n/a
3	chr10:94050143-94050193	NT2-D1	testis:	n/a
4	chr10:94050516-94050566	GM19239	blood:	n/a
5	chr10:94050516-94050566	NH-A	brain:	n/a
6	chr10:94050143-94050193	HRE	kidney:	n/a
7	chr10:94050649-94050699	PFSK-1	brain:	n/a
8	chr10:94050143-94050193	Jurkat	blood:	n/a
9	chr10:94050516-94050566	AG04450	lung:	fetal
10	chr10:94050516-94050566	AG10803	skin:	n/a
11	chr10:94050143-94050193	CMK	blood:	n/a
12	chr10:94050143-94050193	NHBE	bronchial:	n/a
13	chr10:94050649-94050699	ovcar-3	ovarian:	n/a
14	chr10:94050516-94050566	ProgFib	skin:	n/a
15	chr10:94050649-94050699	HEEpiC	esophagus:	n/a
16	chr10:94050649-94050699	NHBE	bronchial:	n/a
17	chr10:94050516-94050566	A549	lung:	n/a
18	chr10:94050516-94050566	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:94050516-94050566	MCF-7	breast:	n/a
20	chr10:94050516-94050566	T-47D	breast:	n/a
21	chr10:94050649-94050699	HUVEC	blood vessel:	n/a
22	chr10:94050516-94050566	HRPEpiC	eye:	n/a
23	chr10:94050649-94050699	HepG2	liver:	n/a
24	chr10:94050143-94050193	AG04449	skin:	fetal
25	chr10:94050516-94050566	ovcar-3	ovarian:	n/a
26	chr10:94050143-94050193	GM12892	blood:	n/a
27	chr10:94050516-94050566	AoSMC	blood vessel:	n/a
28	chr10:94050516-94050566	CMK	blood:	n/a
29	chr10:94050649-94050699	HCF	heart:	n/a
30	chr10:94050516-94050566	SK-N-SH	brain:	n/a
31	chr10:94050649-94050699	T-47D	breast:	n/a
32	chr10:94050649-94050699	AoSMC	blood vessel:	n/a
33	chr10:94050649-94050699	HIPEpiC	eye:	n/a
34	chr10:94050649-94050699	GM06990	blood:	n/a
35	chr10:94050516-94050566	GM12878	blood:	n/a
36	chr10:94050649-94050699	AG04449	skin:	fetal
37	chr10:94050649-94050699	SK-N-SH	brain:	n/a
38	chr10:94050143-94050193	MCF10A-Er-Src	breast:	n/a
39	chr10:94050649-94050699	HNPCEpiC	eye:	n/a
40	chr10:94050516-94050566	Hela-S3	cervix:	n/a
41	chr10:94050143-94050193	T-47D	breast:	n/a
42	chr10:94050516-94050566	HepG2	liver:	n/a
43	chr10:94050649-94050699	NHDF-neo	bronchial:	n/a
44	chr10:94050516-94050566	PFSK-1	brain:	n/a
45	chr10:94050143-94050193	K562	blood:	n/a
46	chr10:94050649-94050699	HRCEpiC	kidney:	n/a
47	chr10:94050516-94050566	HCT-116	colon:	n/a
48	chr10:94050649-94050699	ProgFib	skin:	n/a
49	chr10:94050516-94050566	ECC-1	luminal epithelium:	n/a
50	chr10:94050649-94050699	PANC-1	pancreas:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94002101..94003735-chr10:94050527..94052941,2	K562	blood:
2	chr10:94050268..94050930-chr8:33341952..33342805,2	Hela-S3	cervix:
3	chr10:94048555..94050723-chr10:94056799..94059082,2	K562	blood:
4	chr10:94050380..94051225-chrX:70585319..70586284,2	Hela-S3	cervix:
5	chr10:93998891..94002756-chr10:94046633..94048810,3	MCF-7	breast:
6	chr10:94049633..94050585-chr19:3557462..3558007,2	Hela-S3	cervix:
7	chr10:93948126..93950243-chr10:94048743..94050692,2	K562	blood:
8	chr10:93973011..93976411-chr10:94049477..94051967,3	K562	blood:

No data

Variant related genes	Relation type
MARCH5	TF binding region
MARCH5	CpG island
ENSG00000105988	chromatin interactions
ENSG00000147133	chromatin interactions
ENSG00000198042	chromatin interactions
ENSG00000161091	chromatin interactions
ENSG00000107864	chromatin interactions

Extended variants
information (count: 63 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:63 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573383101	chr10:94048658-94048659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144253578	chr10:94048720-94048721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528866006	chr10:94048773-94048774	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs545252251	chr10:94048810-94048811	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs185375484	chr10:94048847-94048848	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs373650398	chr10:94048869-94048870	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs148297510	chr10:94048925-94048926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369431055	chr10:94049023-94049024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141388751	chr10:94049031-94049032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552443488	chr10:94049065-94049066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559387958	chr10:94049112-94049113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528251536	chr10:94049122-94049123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548417995	chr10:94049123-94049124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189649995	chr10:94049175-94049176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181700935	chr10:94049255-94049256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186770056	chr10:94049256-94049257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550731793	chr10:94049308-94049309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192123484	chr10:94049309-94049310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539112416	chr10:94049310-94049311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553584618	chr10:94049373-94049374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76828556	chr10:94049376-94049377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368667996	chr10:94049489-94049490	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12573385	chr10:94049491-94049492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71025390	chr10:94049515-94049516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183345716	chr10:94049537-94049538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530265441	chr10:94049570-94049571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186595595	chr10:94049585-94049586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535619991	chr10:94049690-94049691	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs11816877	chr10:94049691-94049692	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs200567983	chr10:94049694-94049695	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs139664506	chr10:94049695-94049696	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs377534160	chr10:94049728-94049729	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs575466213	chr10:94049794-94049795	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs542406135	chr10:94049865-94049866	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs189768071	chr10:94049977-94049978	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577922038	chr10:94049982-94049983	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs11186898	chr10:94049988-94049989	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs559562676	chr10:94050019-94050020	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs17107521	chr10:94050073-94050074	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs370731972	chr10:94050097-94050098	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs374912047	chr10:94050102-94050103	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs528415745	chr10:94050196-94050197	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs548530233	chr10:94050215-94050216	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs561851639	chr10:94050244-94050245	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs530769375	chr10:94050296-94050297	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs550650065	chr10:94050330-94050331	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs139744800	chr10:94050357-94050358	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs532900835	chr10:94050359-94050360	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs546295195	chr10:94050384-94050385	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs571062557	chr10:94050431-94050432	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
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
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94020200-94049800	Weak transcription	Brain Anterior Caudate	brain
2	chr10:94025800-94049800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr10:94039200-94048800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr10:94039200-94049600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:94039800-94049600	Weak transcription	Right Atrium	heart
6	chr10:94043200-94049800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr10:94044200-94049200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr10:94044200-94050000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:94044400-94049800	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr10:94044400-94049800	Weak transcription	Brain Substantia Nigra	brain
11	chr10:94044400-94049800	Weak transcription	Stomach Mucosa	stomach
12	chr10:94044400-94049800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr10:94044600-94049800	Weak transcription	Fetal Intestine Small	intestine
14	chr10:94044800-94049800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr10:94045000-94049800	Weak transcription	Primary B cells from peripheral blood	blood
16	chr10:94045000-94049800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr10:94045000-94049800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr10:94045000-94049800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr10:94045000-94049800	Weak transcription	GM12878-XiMat	blood
20	chr10:94046000-94050000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr10:94047600-94049800	Weak transcription	Colon Smooth Muscle	Colon
22	chr10:94048600-94049000	Enhancers	Pancreas	Pancrea
23	chr10:94048600-94049200	Enhancers	Lung	lung
24	chr10:94048800-94049000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:94048800-94049000	Enhancers	Aorta	Aorta
26	chr10:94048800-94049000	Enhancers	Brain Angular Gyrus	brain
27	chr10:94048800-94049000	Enhancers	Esophagus	oesophagus
28	chr10:94048800-94049000	Enhancers	Fetal Muscle Trunk	muscle
29	chr10:94048800-94049000	Enhancers	Left Ventricle	heart
30	chr10:94048800-94049000	Enhancers	Ovary	ovary
31	chr10:94048800-94049000	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr10:94048800-94049600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr10:94049000-94049800	Weak transcription	Ovary	ovary
34	chr10:94049000-94049800	Weak transcription	Pancreas	Pancrea
35	chr10:94049000-94049800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr10:94049000-94050000	Weak transcription	Esophagus	oesophagus
37	chr10:94049000-94050000	Weak transcription	Left Ventricle	heart
38	chr10:94049200-94049600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr10:94049200-94049800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:94049200-94049800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr10:94049200-94050000	Weak transcription	Lung	lung
42	chr10:94049400-94049600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr10:94049400-94049600	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr10:94049600-94049800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr10:94049600-94049800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr10:94049600-94049800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr10:94049600-94049800	Enhancers	Primary B cells from cord blood	blood
48	chr10:94049600-94049800	Enhancers	Primary T cells from cord blood	blood
49	chr10:94049600-94049800	Enhancers	Primary T cells fromperipheralblood	blood
50	chr10:94049600-94049800	Enhancers	Primary hematopoietic stem cells	blood

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