Variant report

Variant	esv1845799
Chromosome Location	chr1:158175976-158230829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:184)
CpG islands
(count:245)
Chromatin interactive
region (count:6)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:184 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:158217850-158218281	GM12878	blood:	n/a	n/a
2	BATF	chr1:158216589-158216761	GM12878	blood:	n/a	n/a
3	BCL11A	chr1:158178671-158178874	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:158183251-158183479	A549	lung:	n/a	chr1:158183379-158183390
5	CEBPB	chr1:158183220-158183477	HepG2	liver:	n/a	chr1:158183379-158183390
6	CEBPB	chr1:158221829-158221952	A549	lung:	n/a	n/a
7	CEBPB	chr1:158215112-158215534	A549	lung:	n/a	n/a
8	CEBPB	chr1:158215057-158215474	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:158215437-158215445	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr1:158216542-158216739	GM13977	blood:	n/a	n/a
11	CTCF	chr1:158216453-158216817	GM12878	blood:	n/a	n/a
12	CTCF	chr1:158216646-158216691	GM19239	blood:	n/a	n/a
13	CTCF	chr1:158216460-158216610	GM12866	blood:	n/a	n/a
14	CTCF	chr1:158183718-158183788	Fibrobl	skin:	n/a	n/a
15	CTCF	chr1:158216721-158216772	MCF-7	breast:	n/a	n/a
16	CTCF	chr1:158216520-158216670	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr1:158216392-158216815	HCT-116	colon:	n/a	n/a
18	CTCF	chr1:158230080-158230230	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr1:158216690-158216796	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:158216680-158216830	GM12864	blood:	n/a	n/a
21	CTCF	chr1:158216375-158216856	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:158216560-158216775	GM10266	blood:	n/a	n/a
23	CTCF	chr1:158216620-158216770	RPTEC	kidney:	n/a	n/a
24	CTCF	chr1:158216577-158216615	GM10248	blood:	n/a	n/a
25	CTCF	chr1:158216660-158216763	GM12892	blood:	n/a	n/a
26	CTCF	chr1:158216612-158216631	HepG2	liver:	n/a	n/a
27	CTCF	chr1:158203493-158203536	GM20000	blood:	n/a	n/a
28	CTCF	chr1:158216511-158216820	T-47D	breast:	n/a	n/a
29	CTCF	chr1:158216655-158216721	GM19238	blood:	n/a	n/a
30	CTCF	chr1:158216500-158216650	GM12869	blood:	n/a	n/a
31	CTCF	chr1:158216500-158216650	GM12873	blood:	n/a	n/a
32	CTCF	chr1:158216520-158216670	GM12875	blood:	n/a	n/a
33	CTCF	chr1:158216500-158216650	GM12872	blood:	n/a	n/a
34	CTCF	chr1:158216520-158216670	GM12871	blood:	n/a	n/a
35	CTCF	chr1:158216554-158216801	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr1:158216563-158216779	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:158216560-158216710	SAEC	small airway:	n/a	n/a
38	CTCF	chr1:158199286-158199327	GM10248	blood:	n/a	n/a
39	CTCF	chr1:158216515-158216783	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:158197026-158197066	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr1:158216540-158216690	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:158216504-158216756	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:158216540-158216690	HRE	kidney:	n/a	n/a
44	CTCF	chr1:158216460-158216610	GM12865	blood:	n/a	n/a
45	CTCF	chr1:158216480-158216630	NHEK	skin:	n/a	n/a
46	CTCF	chr1:158216620-158216770	GM12878	blood:	n/a	n/a
47	CTCF	chr1:158216580-158216730	GM12865	blood:	n/a	n/a
48	CTCF	chr1:158216540-158216690	NHEK	skin:	n/a	n/a
49	CTCF	chr1:158216580-158216730	GM12873	blood:	n/a	n/a
50	CTCF	chr1:158216600-158216750	GM12872	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158223934-158223984	Caco-2	colon:	n/a
2	chr1:158223934-158223984	Caco-2	colon:	n/a
3	chr1:158223921-158223971	HMEC	breast:	n/a
4	chr1:158224869-158224919	AG09309	skin:	n/a
5	chr1:158223921-158223971	ovcar-3	ovarian:	n/a
6	chr1:158224869-158224919	MCF-7	breast:	n/a
7	chr1:158223921-158223971	NH-A	brain:	n/a
8	chr1:158223921-158223971	HL-60	blood:	n/a
9	chr1:158223921-158223971	HAEpiC	amniotic membrane:	n/a
10	chr1:158223921-158223971	RPTEC	kidney:	n/a
11	chr1:158223934-158223984	HepG2	liver:	n/a
12	chr1:158224869-158224919	GM06990	blood:	n/a
13	chr1:158224869-158224919	SKMC	muscle:	n/a
14	chr1:158223513-158223563	HAEpiC	amniotic membrane:	n/a
15	chr1:158223934-158223984	SK-N-SH_RA	brain:	n/a
16	chr1:158224869-158224919	HCPEpiC	choroid plexus:	n/a
17	chr1:158223921-158223971	HRCEpiC	kidney:	n/a
18	chr1:158223513-158223563	Caco-2	colon:	n/a
19	chr1:158224869-158224919	HNPCEpiC	eye:	n/a
20	chr1:158224869-158224919	ProgFib	skin:	n/a
21	chr1:158223921-158223971	HCT-116	colon:	n/a
22	chr1:158223921-158223971	Hela-S3	cervix:	n/a
23	chr1:158223934-158223984	SAEC	small airway:	n/a
24	chr1:158223934-158223984	GM12892	blood:	n/a
25	chr1:158224869-158224919	HEEpiC	esophagus:	n/a
26	chr1:158223513-158223563	RPTEC	kidney:	n/a
27	chr1:158223513-158223563	K562	blood:	n/a
28	chr1:158223934-158223984	CMK	blood:	n/a
29	chr1:158223921-158223971	H1-hESC	embryonic stem cell:	embryo
30	chr1:158224869-158224919	NB4	blood:	n/a
31	chr1:158223513-158223563	A549	lung:	n/a
32	chr1:158223921-158223971	ECC-1	luminal epithelium:	n/a
33	chr1:158223934-158223984	SK-N-MC	brain:	n/a
34	chr1:158223513-158223563	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:158223934-158223984	MCF10A-Er-Src	breast:	n/a
36	chr1:158223513-158223563	HRPEpiC	eye:	n/a
37	chr1:158223513-158223563	HEK293	kidney:	embryo
38	chr1:158224869-158224919	U87	brain:	n/a
39	chr1:158224869-158224919	ovcar-3	ovarian:	n/a
40	chr1:158223921-158223971	HIPEpiC	eye:	n/a
41	chr1:158223921-158223971	Jurkat	blood:	n/a
42	chr1:158224869-158224919	PrEC	prostate:	n/a
43	chr1:158223921-158223971	HRE	kidney:	n/a
44	chr1:158224869-158224919	GM19239	blood:	n/a
45	chr1:158223921-158223971	AG04449	skin:	fetal
46	chr1:158223513-158223563	ProgFib	skin:	n/a
47	chr1:158223934-158223984	HRPEpiC	eye:	n/a
48	chr1:158223513-158223563	T-47D	breast:	n/a
49	chr1:158224869-158224919	HRPEpiC	eye:	n/a
50	chr1:158223513-158223563	HNPCEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158215977..158216658-chr1:158299289..158299857,2	MCF-7	breast:
2	chr1:158216297..158216811-chr1:178024086..178024814,2	MCF-7	breast:
3	chr1:158216395..158217146-chr1:158496757..158497397,2	MCF-7	breast:
4	chr1:158159135..158160992-chr1:158182164..158184743,2	K562	blood:
5	chr1:158212629..158214182-chr1:158216641..158218801,2	K562	blood:
6	chr1:158212629..158214182-chr1:158216641..158218801,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD1A-1	chr1:158213058-158213526	NONHSAT006977
2	lnc-CD1A-1	chr1:158213058-158213358	ucscGeneNc_uc001fuu_2
3	lnc-CD1A-1	chr1:158213058-158213526	NONHSAT006976
4	lnc-CD1A-1	chr1:158197698-158197819	ucscGeneNc_uc001fuu_2
5	lnc-CD1A-1	chr1:158201913-158202059	NONHSAT006976
6	lnc-CD1A-1	chr1:158197638-158197819	NONHSAT006977
7	lnc-CD1A-1	chr1:158197632-158197819	NONHSAT006976
8	lnc-CD1A-1	chr1:158215014-158215475	NONHSAT006977

No data

Variant related genes	Relation type
ENSG00000176320	TF binding region
CD1A	TF binding region
ENSG00000176320	CpG island
CD1A	CpG island

Extended variants
information (count: 1385 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1385 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529367494	chr1:158176003-158176004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs421484	chr1:158176028-158176029	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs374446538	chr1:158176070-158176071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs386368427	chr1:158176071-158176072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386368428	chr1:158176077-158176078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs397821558	chr1:158176078-158176079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142406610	chr1:158176113-158176114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151290053	chr1:158176121-158176122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139432138	chr1:158176132-158176133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112775318	chr1:158176166-158176167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs422944	chr1:158176171-158176172	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs442076	chr1:158176231-158176232	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567891407	chr1:158176263-158176264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535242737	chr1:158176292-158176293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141946970	chr1:158176343-158176344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12738901	chr1:158176356-158176357	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs71084266	chr1:158176367-158176368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs398103273	chr1:158176379-158176380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73014155	chr1:158176412-158176413	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs189254097	chr1:158176439-158176440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs692052	chr1:158176443-158176444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs561553072	chr1:158176488-158176489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561896453	chr1:158176533-158176534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554574130	chr1:158176536-158176537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572652822	chr1:158176564-158176565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540057358	chr1:158176609-158176610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555401185	chr1:158176620-158176621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112713093	chr1:158176622-158176623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs59279563	chr1:158176628-158176629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs590018	chr1:158176652-158176653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544979867	chr1:158176671-158176672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112183406	chr1:158176674-158176675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531101951	chr1:158176712-158176713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371110074	chr1:158176718-158176719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540793012	chr1:158176724-158176725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs367984426	chr1:158176725-158176726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528669325	chr1:158176730-158176731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61580508	chr1:158176737-158176738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201467188	chr1:158176738-158176739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144866360	chr1:158176789-158176790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571352067	chr1:158176806-158176807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1238748	chr1:158176828-158176829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538769749	chr1:158176876-158176877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs591331	chr1:158176931-158176932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35192840	chr1:158176965-158176966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556681777	chr1:158176985-158176986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1748386	chr1:158177006-158177007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs55819216	chr1:158177046-158177047	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs369413237	chr1:158177047-158177048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78801939	chr1:158177069-158177070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158173800-158178200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr1:158173800-158178200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr1:158173800-158178400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:158174200-158177200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr1:158174600-158182600	Weak transcription	Thymus	Thymus
6	chr1:158175400-158176000	Enhancers	Dnd41	blood
7	chr1:158176000-158178600	Weak transcription	Dnd41	blood
8	chr1:158177400-158178200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr1:158178200-158179400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:158178200-158179400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr1:158178200-158179400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr1:158178400-158179000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr1:158178400-158179400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr1:158178400-158179400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr1:158178400-158179600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:158178600-158179000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:158178600-158179400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:158178600-158179400	Enhancers	Dnd41	blood
19	chr1:158179400-158181600	Weak transcription	Dnd41	blood
20	chr1:158179400-158182000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr1:158179400-158182600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:158181600-158182200	Enhancers	Dnd41	blood
23	chr1:158182000-158182200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr1:158182000-158182400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:158182000-158182600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:158182200-158182600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr1:158182200-158182600	Weak transcription	Dnd41	blood
28	chr1:158182200-158184000	ZNF genes & repeats	Lung	lung
29	chr1:158182400-158183200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:158182600-158182800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:158182600-158183800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:158182600-158184200	ZNF genes & repeats	Dnd41	blood
33	chr1:158183600-158183800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr1:158194200-158198400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr1:158198400-158198600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:158206800-158207200	Enhancers	Dnd41	blood
37	chr1:158213600-158213800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr1:158213800-158214200	Enhancers	Thymus	Thymus
39	chr1:158214000-158217400	Enhancers	Dnd41	blood
40	chr1:158214200-158214600	Weak transcription	Thymus	Thymus
41	chr1:158214600-158215600	Enhancers	Thymus	Thymus
42	chr1:158214800-158217400	Enhancers	Fetal Thymus	thymus
43	chr1:158215000-158215200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
44	chr1:158215000-158215200	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr1:158215400-158215600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
46	chr1:158215400-158215600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
47	chr1:158215600-158216600	Weak transcription	Thymus	Thymus
48	chr1:158216400-158217000	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr1:158216400-158217400	Enhancers	Fetal Heart	heart
50	chr1:158216400-158222400	Enhancers	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links