Variant report

Variant	esv3356894
Chromosome Location	chr1:227985266-228005245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:225)
CpG islands
(count:549)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:225 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:227986998-227987305	K562	blood:	n/a	n/a
2	ATF3	chr1:228003217-228003449	K562	blood:	n/a	n/a
3	BACH1	chr1:227996473-227996564	K562	blood:	n/a	n/a
4	BRCA1	chr1:227993242-227993704	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr1:228003121-228003526	K562	blood:	n/a	n/a
6	CBX3	chr1:228001542-228002075	K562	blood:	n/a	n/a
7	CBX3	chr1:228001453-228002244	K562	blood:	n/a	n/a
8	CBX3	chr1:227993132-227994273	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:227993189-227994028	HCT-116	colon:	n/a	n/a
10	CEBPB	chr1:228000148-228000228	HepG2	liver:	n/a	chr1:228000177-228000188
11	CEBPB	chr1:227987533-227987696	HepG2	liver:	n/a	chr1:227987565-227987576
12	CHD2	chr1:227993361-227993823	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr1:227993300-227993450	NHEK	skin:	n/a	n/a
14	CTCF	chr1:228003244-228003465	K562	blood:	n/a	chr1:228003391-228003404
15	CTCF	chr1:228003240-228003390	GM12871	blood:	n/a	n/a
16	CTCF	chr1:228003231-228003338	A549	lung:	n/a	n/a
17	CTCF	chr1:228003247-228003461	H1-hESC	embryonic stem cell:	n/a	chr1:228003391-228003404
18	CTCF	chr1:228003073-228003568	K562	blood:	n/a	chr1:228003391-228003404
19	CTCF	chr1:228003260-228003410	HEK293	kidney:	n/a	chr1:228003391-228003404
20	CTCF	chr1:227993300-227993450	HMF	breast:	n/a	n/a
21	CTCF	chr1:228003140-228003290	HAc	cerebellar:	n/a	n/a
22	CTCF	chr1:228003220-228003370	GM12864	blood:	n/a	n/a
23	CTCF	chr1:228003360-228003510	A549	lung:	n/a	chr1:228003391-228003404
24	CTCF	chr1:228003252-228003443	HepG2	liver:	n/a	chr1:228003391-228003404
25	CTCF	chr1:227993420-227993570	HMEC	breast:	n/a	n/a
26	CTCF	chr1:228003240-228003390	GM12872	blood:	n/a	n/a
27	CTCF	chr1:227993360-227993510	HAc	cerebellar:	n/a	n/a
28	CTCF	chr1:228003159-228003533	K562	blood:	n/a	chr1:228003391-228003404
29	CTCF	chr1:228003124-228003520	K562	blood:	n/a	chr1:228003391-228003404
30	CTCF	chr1:227993379-227993464	ProgFib	skin:	n/a	n/a
31	CTCF	chr1:228003219-228003373	Gliobla	brain:	n/a	n/a
32	CTCF	chr1:227993260-227993410	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr1:227993380-227993530	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr1:228003240-228003390	K562	blood:	n/a	n/a
35	CTCF	chr1:228003120-228003270	GM12872	blood:	n/a	n/a
36	CTCF	chr1:228003320-228003470	K562	blood:	n/a	chr1:228003391-228003404
37	CTCF	chr1:228003269-228003360	GM19239	blood:	n/a	n/a
38	CTCF	chr1:228003201-228003555	K562	blood:	n/a	chr1:228003391-228003404
39	CTCF	chr1:228003230-228003338	Fibrobl	skin:	n/a	n/a
40	CTCF	chr1:227993260-227993410	HPF	lung:	n/a	n/a
41	CTCF	chr1:227993400-227993550	HMF	breast:	n/a	n/a
42	CTCF	chr1:227993317-227993504	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:227993365-227993502	Fibrobl	skin:	n/a	n/a
44	CTCF	chr1:228003286-228003320	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:227993260-227993410	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr1:228003263-228003339	NHEK	skin:	n/a	n/a
47	CTCF	chr1:228003270-228003344	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr1:227992993-227993886	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:227993425-227993458	A549	lung:	n/a	n/a
50	CTCF	chr1:227993300-227993450	AG10803	skin:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228003435-228003485	MCF10A-Er-Src	breast:	n/a
2	chr1:228004075-228004125	HEK293	kidney:	embryo
3	chr1:228003435-228003485	NT2-D1	testis:	n/a
4	chr1:228004075-228004125	HRE	kidney:	n/a
5	chr1:228003938-228003988	K562	blood:	n/a
6	chr1:228003402-228003452	HCT-116	colon:	n/a
7	chr1:228004967-228005017	H1-hESC	embryonic stem cell:	embryo
8	chr1:228003900-228003950	NB4	blood:	n/a
9	chr1:228004967-228005017	ECC-1	luminal epithelium:	n/a
10	chr1:228003402-228003452	MCF-7	breast:	n/a
11	chr1:228003435-228003485	A549	lung:	n/a
12	chr1:228004967-228005017	SAEC	small airway:	n/a
13	chr1:228004967-228005017	NB4	blood:	n/a
14	chr1:228003402-228003452	SKMC	muscle:	n/a
15	chr1:228004967-228005017	PrEC	prostate:	n/a
16	chr1:228003402-228003452	NT2-D1	testis:	n/a
17	chr1:228003402-228003452	HCF	heart:	n/a
18	chr1:228003900-228003950	PANC-1	pancreas:	n/a
19	chr1:228003435-228003485	HepG2	liver:	n/a
20	chr1:228003072-228003122	HAEpiC	amniotic membrane:	n/a
21	chr1:228003938-228003988	AG09309	skin:	n/a
22	chr1:228004967-228005017	HAEpiC	amniotic membrane:	n/a
23	chr1:228003072-228003122	HCM	heart:	n/a
24	chr1:228001655-228001705	AG04450	lung:	fetal
25	chr1:228003435-228003485	SAEC	small airway:	n/a
26	chr1:228003402-228003452	BJ	skin:	n/a
27	chr1:228001655-228001705	PrEC	prostate:	n/a
28	chr1:228003938-228003988	HCF	heart:	n/a
29	chr1:228003072-228003122	GM12878	blood:	n/a
30	chr1:228001655-228001705	LNCaP	prostate:	n/a
31	chr1:228003393-228003443	Caco-2	colon:	n/a
32	chr1:228001655-228001705	MCF10A-Er-Src	breast:	n/a
33	chr1:228003435-228003485	Hela-S3	cervix:	n/a
34	chr1:228003938-228003988	Hela-S3	cervix:	n/a
35	chr1:228003393-228003443	ProgFib	skin:	n/a
36	chr1:228001655-228001705	A549	lung:	n/a
37	chr1:228003435-228003485	GM12878	blood:	n/a
38	chr1:228004967-228005017	HEEpiC	esophagus:	n/a
39	chr1:228003900-228003950	HEK293	kidney:	embryo
40	chr1:228001655-228001705	T-47D	breast:	n/a
41	chr1:228003402-228003452	SK-N-SH_RA	brain:	n/a
42	chr1:228004967-228005017	HCM	heart:	n/a
43	chr1:228003402-228003452	HMEC	breast:	n/a
44	chr1:228003393-228003443	HCT-116	colon:	n/a
45	chr1:228003938-228003988	HAEpiC	amniotic membrane:	n/a
46	chr1:228003900-228003950	HRPEpiC	eye:	n/a
47	chr1:228001655-228001705	HCT-116	colon:	n/a
48	chr1:228001655-228001705	SK-N-SH_RA	brain:	n/a
49	chr1:228001655-228001705	BJ	skin:	n/a
50	chr1:228004967-228005017	BJ	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227950165..227950767-chr1:227991014..227991675,2	K562	blood:
2	chr1:227987307..227988833-chr1:227989105..227991204,2	MCF-7	breast:
3	chr1:227977112..227980203-chr1:227982448..227986232,4	MCF-7	breast:
4	chr1:227987307..227988833-chr1:227989105..227991204,2	MCF-7	breast:
5	chr1:228003528..228005647-chr1:228006569..228009542,2	K562	blood:
6	chr1:227985977..227987965-chr1:228133584..228136071,2	K562	blood:
7	chr1:227992970..227993567-chr1:228129726..228130492,2	MCF-7	breast:

No data

Variant related genes	Relation type
PRSS38	TF binding region
PRSS38	CpG island
ENSG00000143816	chromatin interactions

Extended variants
information (count: 530 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372893654	chr1:227986026-227986027	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs79144879	chr1:227986040-227986041	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs576932743	chr1:227986041-227986042	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs541065410	chr1:227986053-227986054	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs552674104	chr1:227986069-227986070	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs138713700	chr1:227986083-227986084	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542943289	chr1:227986093-227986094	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561541086	chr1:227986112-227986113	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531744987	chr1:227986124-227986125	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543531778	chr1:227986152-227986153	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116727962	chr1:227986196-227986197	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529362439	chr1:227986197-227986198	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs142713557	chr1:227986199-227986200	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565925143	chr1:227986202-227986203	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530009176	chr1:227986240-227986241	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371865437	chr1:227986243-227986244	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs376123193	chr1:227986289-227986290	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548135058	chr1:227986298-227986299	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77704522	chr1:227986299-227986300	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537205650	chr1:227986404-227986405	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552388769	chr1:227986413-227986414	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570591425	chr1:227986421-227986422	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs368859429	chr1:227986422-227986423	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534706836	chr1:227986450-227986451	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147358328	chr1:227986463-227986464	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181982505	chr1:227986474-227986475	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75617281	chr1:227986532-227986533	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554937245	chr1:227986539-227986540	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111478466	chr1:227986548-227986549	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs191903468	chr1:227986570-227986571	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75364737	chr1:227986599-227986600	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs12750005	chr1:227986661-227986662	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76554499	chr1:227986663-227986664	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559699401	chr1:227986667-227986668	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539232404	chr1:227986685-227986686	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369986162	chr1:227986734-227986735	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs115740315	chr1:227986809-227986810	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570317063	chr1:227986822-227986823	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563611996	chr1:227986900-227986901	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531241090	chr1:227986906-227986907	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs530806766	chr1:227986912-227986913	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs12091509	chr1:227986939-227986940	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs567886095	chr1:227986946-227986947	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566187121	chr1:227986980-227986981	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs142722024	chr1:227987000-227987001	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554578506	chr1:227987051-227987052	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534718888	chr1:227987192-227987193	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139001648	chr1:227987205-227987206	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs149539369	chr1:227987237-227987238	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs371334561	chr1:227987251-227987252	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
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
Breast cancer	17603634	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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227986000-227986200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:227986200-227987000	Enhancers	K562	blood
3	chr1:227986600-227987000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:227990200-227990400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:227990400-227997800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:227992800-227993000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:227993000-227994200	Enhancers	NHEK	skin
8	chr1:227993000-227994400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:227993000-227994400	Enhancers	HMEC	breast
10	chr1:227993200-227994200	Enhancers	NH-A	brain
11	chr1:227993200-227994400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr1:227993200-227994600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:227993400-227993600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
14	chr1:227993400-227993800	Enhancers	HSMM	muscle
15	chr1:227993400-227994000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:227993400-227994000	Enhancers	HSMMtube	muscle
17	chr1:227993600-227993800	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr1:227993600-227994000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:227993600-227994000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:227993600-227994000	Enhancers	Colon Smooth Muscle	Colon
21	chr1:227993600-227994000	Enhancers	NHLF	lung
22	chr1:227993600-227994200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:227993600-227994400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:227993600-227994400	Enhancers	Hela-S3	cervix
25	chr1:227993600-227994400	Enhancers	Osteobl	bone
26	chr1:227993800-227994000	Weak transcription	HSMM	muscle
27	chr1:227994000-227994400	Enhancers	HSMM	muscle
28	chr1:227994400-227994600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:227994400-227996000	Weak transcription	HMEC	breast
30	chr1:227994400-227996200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr1:227995800-227996600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:227996000-227996600	Enhancers	HMEC	breast
33	chr1:227996200-227996800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr1:227996400-227996600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:227996400-227996600	Enhancers	HSMM	muscle
36	chr1:227996400-227996800	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr1:227996400-227996800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr1:227996400-227996800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr1:227996400-227996800	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr1:227996400-227997000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr1:227996400-227997000	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr1:228001400-228002000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:228003200-228005000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:228003800-228005400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:228004200-228005400	Enhancers	Primary T cells fromperipheralblood	blood
46	chr1:228004600-228005000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr1:228004600-228005200	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr1:228004600-228005400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr1:228005000-228005200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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