Variant report

Variant	esv1798515
Chromosome Location	chr1:220157811-220167371
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	chr1:220164343-220164674	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:220167031-220167220	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:220164368-220164700	K562	blood:	n/a	n/a
4	ATF1	chr1:220159572-220159639	K562	blood:	n/a	n/a
5	ATF2	chr1:220161520-220162244	GM12878	blood:	n/a	n/a
6	BATF	chr1:220161821-220162147	GM12878	blood:	n/a	n/a
7	BCLAF1	chr1:220161550-220162282	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:220158687-220158770	GM12878	blood:	n/a	n/a
9	CCNT2	chr1:220161065-220161211	K562	blood:	n/a	n/a
10	CCNT2	chr1:220165024-220165335	K562	blood:	n/a	n/a
11	CEBPB	chr1:220159572-220159724	A549	lung:	n/a	n/a
12	CEBPB	chr1:220159606-220159651	K562	blood:	n/a	n/a
13	CEBPB	chr1:220163851-220163996	K562	blood:	n/a	n/a
14	CTCF	chr1:220164460-220164610	SK-N-SH_RA	brain:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
15	CTCF	chr1:220164480-220164630	HVMF	connective:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
16	CTCF	chr1:220164400-220164550	HepG2	liver:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
17	CTCF	chr1:220164397-220164680	Medullo	brain:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
18	CTCF	chr1:220164440-220164590	MCF-7	breast:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
19	CTCF	chr1:220164440-220164590	HMEC	breast:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
20	CTCF	chr1:220164440-220164590	GM12866	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
21	CTCF	chr1:220164460-220164610	AoAF	blood vessel:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
22	CTCF	chr1:220164440-220164590	HFF-Myc	foreskin:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
23	CTCF	chr1:220164435-220164672	HepG2	liver:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
24	CTCF	chr1:220164358-220164741	K562	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
25	CTCF	chr1:220164420-220164570	GM12865	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
26	CTCF	chr1:220164420-220164570	HA-sp	spinal cord:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
27	CTCF	chr1:220164500-220164650	GM12873	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
28	CTCF	chr1:220164330-220164695	A549	lung:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
29	CTCF	chr1:220164452-220164576	SK-N-SH_RA	brain:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
30	CTCF	chr1:220164500-220164650	BJ	skin:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
31	CTCF	chr1:220164440-220164590	HCPEpiC	choroid plexus:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
32	CTCF	chr1:220164451-220164591	LNCaP	prostate:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
33	CTCF	chr1:220164400-220164550	NHEK	skin:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
34	CTCF	chr1:220164440-220164590	NB4	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
35	CTCF	chr1:220164500-220164650	GM12872	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
36	CTCF	chr1:220164420-220164570	AG04450	lung:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
37	CTCF	chr1:220164480-220164630	GM12874	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
38	CTCF	chr1:220164403-220164592	HepG2	liver:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
39	CTCF	chr1:220164460-220164610	HMF	breast:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
40	CTCF	chr1:220164420-220164570	NHDF-neo	bronchial:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
41	CTCF	chr1:220164400-220164550	HRE	kidney:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
42	CTCF	chr1:220164283-220164654	MCF-7	breast:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
43	CTCF	chr1:220164440-220164590	BJ	skin:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
44	CTCF	chr1:220164342-220164795	IMR90	lung:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
45	CTCF	chr1:220164400-220164550	HEK293	kidney:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
46	CTCF	chr1:220164440-220164590	HCT-116	colon:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
47	CTCF	chr1:220164104-220165175	A549	lung:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
48	CTCF	chr1:220164432-220164634	Kidney_OC	kidney:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
49	CTCF	chr1:220164480-220164630	AG04450	lung:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
50	CTCF	chr1:220164460-220164610	HPF	lung:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542

No.	Distal block	Cell Line	Cell type
1	chr1:220072242..220074837-chr1:220162775..220165302,2	K562	blood:
2	chr1:220166855..220169233-chr1:220184126..220185704,2	K562	blood:
3	chr1:220164810..220167759-chr1:220168424..220170636,2	K562	blood:
4	chr1:220163115..220165079-chr1:220292412..220294107,2	K562	blood:
5	chr1:220049633..220050383-chr1:220164327..220165162,2	MCF-7	breast:
6	chr1:220164112..220164967-chr1:220297177..220297836,2	MCF-7	breast:
7	chr1:220163102..220165191-chr1:220201695..220204471,2	K562	blood:
8	chr1:220153591..220159773-chr1:220159981..220165102,9	K562	blood:
9	chr1:220144163..220148221-chr1:220163054..220166012,3	K562	blood:
10	chr1:220163484..220165362-chr1:220165481..220167153,2	K562	blood:
11	chr1:220163484..220165362-chr1:220165481..220167153,2	K562	blood:
12	chr1:220165101..220168556-chr1:220168858..220170933,3	K562	blood:
13	chr1:220161264..220163445-chr1:220234115..220237098,2	K562	blood:
14	chr1:220153591..220159773-chr1:220159981..220165102,9	K562	blood:
15	chr1:220011035..220013766-chr1:220162762..220165197,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPRS-1	chr1:220158557-220158677	NONHSAT009572
2	lnc-EPRS-1	chr1:220158557-220158677	NONHSAT009569

Variant related genes	Relation type
ENSG00000238798	TF binding region
EPRS	TF binding region
ENSG00000136628	chromatin interactions
ENSG00000238798	chromatin interactions

Extended variants
information (count: 374 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:374 , 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	rs564040121	chr1:220157813-220157814	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs533078226	chr1:220157846-220157847	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs2647437	chr1:220157849-220157850	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs113539774	chr1:220157909-220157910	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs147650655	chr1:220157911-220157912	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs2647436	chr1:220157915-220157916	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs1909199	chr1:220157927-220157928	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561822115	chr1:220157955-220157956	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs115207263	chr1:220158018-220158019	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs115894402	chr1:220158021-220158022	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs114215331	chr1:220158022-220158023	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs372883287	chr1:220158065-220158066	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570733555	chr1:220158070-220158071	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375841680	chr1:220158126-220158127	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12058150	chr1:220158145-220158146	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs186868176	chr1:220158242-220158243	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146446907	chr1:220158243-220158244	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535223869	chr1:220158252-220158253	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550477980	chr1:220158274-220158275	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs571973948	chr1:220158277-220158278	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548071735	chr1:220158296-220158297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs190166948	chr1:220158301-220158302	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182347579	chr1:220158305-220158306	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577560056	chr1:220158334-220158335	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543553373	chr1:220158335-220158336	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs2486328	chr1:220158339-220158340	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs576720993	chr1:220158341-220158342	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs140473502	chr1:220158342-220158343	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12059273	chr1:220158349-220158350	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs2454326	chr1:220158369-220158370	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs548093070	chr1:220158390-220158391	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs145581165	chr1:220158391-220158392	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs138252265	chr1:220158400-220158401	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs189539765	chr1:220158404-220158405	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs180934352	chr1:220158455-220158456	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149200257	chr1:220158483-220158484	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548738201	chr1:220158490-220158491	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565525128	chr1:220158535-220158536	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374960520	chr1:220158538-220158539	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs557766753	chr1:220158545-220158546	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs367762945	chr1:220158552-220158553	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs536603040	chr1:220158579-220158580	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs557035063	chr1:220158683-220158684	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs573752222	chr1:220158830-220158831	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145149599	chr1:220158838-220158839	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs562302578	chr1:220158844-220158845	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369970973	chr1:220158845-220158846	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs541755640	chr1:220158855-220158856	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs116426251	chr1:220158856-220158857	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs185340911	chr1:220158858-220158859	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220132800-220177000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:220140000-220167400	Weak transcription	Gastric	stomach
3	chr1:220140200-220160000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:220140600-220162400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:220140600-220162400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr1:220140600-220163000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:220140800-220161800	Strong transcription	Fetal Thymus	thymus
8	chr1:220140800-220162400	Strong transcription	Fetal Intestine Large	intestine
9	chr1:220140800-220162400	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr1:220140800-220163200	Strong transcription	Primary T cells from cord blood	blood
11	chr1:220140800-220164000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:220140800-220173400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:220140800-220192400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:220141000-220158000	Strong transcription	Primary B cells from peripheral blood	blood
15	chr1:220141000-220163000	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:220141000-220163200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:220141000-220163400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:220141200-220158200	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr1:220141200-220162000	Strong transcription	Adipose Nuclei	Adipose
20	chr1:220141200-220162800	Strong transcription	Duodenum Mucosa	Duodenum
21	chr1:220141200-220163200	Strong transcription	HSMM	muscle
22	chr1:220141200-220192200	Weak transcription	Fetal Kidney	kidney
23	chr1:220141400-220161800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:220141400-220162000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:220141400-220162200	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr1:220141400-220162200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr1:220141400-220163400	Strong transcription	Dnd41	blood
28	chr1:220141400-220165400	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr1:220141600-220158000	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr1:220141600-220162000	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr1:220141600-220162200	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr1:220142200-220164000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr1:220142600-220169400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr1:220145800-220162000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr1:220146400-220182800	Weak transcription	Spleen	Spleen
36	chr1:220146600-220158800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:220146600-220160400	Weak transcription	Psoas Muscle	Psoas
38	chr1:220147200-220169400	Weak transcription	Fetal Heart	heart
39	chr1:220147800-220163400	Strong transcription	K562	blood
40	chr1:220148200-220162200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr1:220148400-220162400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:220148600-220161800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:220148600-220162000	Strong transcription	Osteobl	bone
44	chr1:220148600-220162200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:220149000-220158000	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr1:220149000-220161000	Strong transcription	Colon Smooth Muscle	Colon
47	chr1:220149000-220167400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:220149200-220158200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr1:220149200-220163400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:220149400-220162200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood

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