Variant report

Variant	nsv1031672
Chromosome Location	chr8:52872448-52917469
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	chr8:52885937-52886571	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:52899570-52899849	HepG2	liver:	n/a	n/a
3	ATF2	chr8:52874345-52875476	GM12878	blood:	n/a	n/a
4	ATF2	chr8:52874536-52875346	GM12878	blood:	n/a	n/a
5	BATF	chr8:52874748-52875028	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:52874691-52875195	GM12878	blood:	n/a	n/a
7	BCLAF1	chr8:52874480-52875556	GM12878	blood:	n/a	chr8:52875215-52875222
8	BHLHE40	chr8:52874894-52875372	K562	blood:	n/a	n/a
9	BHLHE40	chr8:52898365-52898494	K562	blood:	n/a	n/a
10	BHLHE40	chr8:52912955-52912981	K562	blood:	n/a	n/a
11	BHLHE40	chr8:52874580-52875605	GM12878	blood:	n/a	n/a
12	BRCA1	chr8:52874272-52874367	GM12878	blood:	n/a	n/a
13	BRCA1	chr8:52908446-52908632	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr8:52874591-52875729	GM12878	blood:	n/a	n/a
15	CEBPB	chr8:52908062-52908326	IMR90	lung:	n/a	chr8:52908217-52908228 chr8:52908219-52908228 chr8:52908219-52908230
16	CEBPB	chr8:52899935-52900110	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:52875517-52875812	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:52875448-52875868	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:52892569-52892637	HepG2	liver:	n/a	chr8:52892595-52892606
20	CEBPB	chr8:52901158-52901483	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:52892446-52892881	MCF-7	breast:	n/a	chr8:52892595-52892606
22	CEBPB	chr8:52892428-52892787	MCF-7	breast:	n/a	chr8:52892595-52892606
23	CEBPB	chr8:52876554-52876868	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:52907706-52908343	HepG2	liver:	n/a	chr8:52908217-52908228 chr8:52908219-52908228 chr8:52908219-52908230
25	CEBPB	chr8:52895346-52895633	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr8:52874846-52875938	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:52907742-52908369	K562	blood:	n/a	chr8:52908217-52908228 chr8:52908219-52908228 chr8:52908219-52908230
28	CEBPZ	chr8:52886001-52886418	HepG2	liver:	n/a	n/a
29	CHD1	chr8:52874568-52875437	GM12878	blood:	n/a	n/a
30	CHD2	chr8:52873930-52875395	GM12878	blood:	n/a	n/a
31	CHD2	chr8:52875505-52875791	Hela-S3	cervix:	n/a	n/a
32	CREB1	chr8:52874729-52875278	GM12878	blood:	n/a	n/a
33	CTCF	chr8:52891000-52891236	K562	blood:	n/a	chr8:52891102-52891120 chr8:52891105-52891115 chr8:52891097-52891118 chr8:52891104-52891117
34	CTCF	chr8:52916760-52916910	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr8:52874324-52874424	GM12891	blood:	n/a	n/a
36	CTCF	chr8:52916720-52916870	HFF	foreskin:	n/a	n/a
37	CTCF	chr8:52896841-52896871	Fibrobl	skin:	n/a	n/a
38	CTCF	chr8:52891107-52891179	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:52891080-52891230	HUVEC	blood vessel:	n/a	chr8:52891102-52891120 chr8:52891105-52891115 chr8:52891097-52891118 chr8:52891104-52891117
40	CTCF	chr8:52901600-52901750	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr8:52916744-52916856	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:52916749-52916847	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:52901540-52901690	HPF	lung:	n/a	n/a
44	CTCF	chr8:52891108-52891158	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:52910896-52910965	Fibrobl	skin:	n/a	n/a
46	CTCF	chr8:52891079-52891147	Lung_OC	lung:	n/a	chr8:52891102-52891120 chr8:52891105-52891115 chr8:52891097-52891118 chr8:52891104-52891117
47	CTCF	chr8:52891014-52891193	HUVEC	blood vessel:	n/a	chr8:52891102-52891120 chr8:52891105-52891115 chr8:52891097-52891118 chr8:52891104-52891117
48	CTCF	chr8:52891041-52891199	Spleen_OC	spleen:	n/a	chr8:52891102-52891120 chr8:52891105-52891115 chr8:52891097-52891118 chr8:52891104-52891117
49	CTCF	chr8:52891020-52891170	HMEC	breast:	n/a	chr8:52891102-52891120 chr8:52891105-52891115 chr8:52891097-52891118 chr8:52891104-52891117
50	CTCF	chr8:52891040-52891190	HMEC	breast:	n/a	chr8:52891102-52891120 chr8:52891105-52891115 chr8:52891097-52891118 chr8:52891104-52891117

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:52874692-52874742	GM06990	blood:	n/a
2	chr8:52874692-52874742	GM06990	blood:	n/a
3	chr8:52874692-52874742	CMK	blood:	n/a
4	chr8:52874692-52874742	MCF-7	breast:	n/a
5	chr8:52874692-52874742	SK-N-SH_RA	brain:	n/a
6	chr8:52874692-52874742	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:52874692-52874742	NT2-D1	testis:	n/a
8	chr8:52874692-52874742	Caco-2	colon:	n/a
9	chr8:52874692-52874742	BJ	skin:	n/a
10	chr8:52874692-52874742	Hela-S3	cervix:	n/a
11	chr8:52874692-52874742	NB4	blood:	n/a
12	chr8:52874692-52874742	SK-N-SH	brain:	n/a
13	chr8:52874692-52874742	HEEpiC	esophagus:	n/a
14	chr8:52874692-52874742	HRPEpiC	eye:	n/a
15	chr8:52874692-52874742	HNPCEpiC	eye:	n/a
16	chr8:52874692-52874742	HMEC	breast:	n/a
17	chr8:52874692-52874742	AoSMC	blood vessel:	n/a
18	chr8:52874692-52874742	LNCaP	prostate:	n/a
19	chr8:52874692-52874742	NHBE	bronchial:	n/a
20	chr8:52874692-52874742	U87	brain:	n/a
21	chr8:52874692-52874742	Hepatocyte	liver:	n/a
22	chr8:52874692-52874742	BE2_C	brain:	n/a
23	chr8:52874692-52874742	GM12892	blood:	n/a
24	chr8:52874692-52874742	HRE	kidney:	n/a
25	chr8:52874692-52874742	HRCEpiC	kidney:	n/a
26	chr8:52874692-52874742	ovcar-3	ovarian:	n/a
27	chr8:52874692-52874742	AG04450	lung:	fetal
28	chr8:52874692-52874742	Jurkat	blood:	n/a
29	chr8:52874692-52874742	HL-60	blood:	n/a
30	chr8:52874692-52874742	AG09319	gingival:	n/a
31	chr8:52874692-52874742	HCF	heart:	n/a
32	chr8:52874692-52874742	IMR90	lung:	fetal
33	chr8:52874692-52874742	HAEpiC	amniotic membrane:	n/a
34	chr8:52874692-52874742	T-47D	breast:	n/a
35	chr8:52874692-52874742	SKMC	muscle:	n/a
36	chr8:52874692-52874742	NH-A	brain:	n/a
37	chr8:52874692-52874742	RPTEC	kidney:	n/a
38	chr8:52874692-52874742	HCM	heart:	n/a
39	chr8:52874692-52874742	GM12878	blood:	n/a
40	chr8:52874692-52874742	SK-N-MC	brain:	n/a
41	chr8:52874692-52874742	A549	lung:	n/a
42	chr8:52874692-52874742	HCT-116	colon:	n/a
43	chr8:52874692-52874742	MCF10A-Er-Src	breast:	n/a
44	chr8:52874692-52874742	AG04449	skin:	fetal
45	chr8:52874692-52874742	PANC-1	pancreas:	n/a
46	chr8:52874692-52874742	PFSK-1	brain:	n/a
47	chr8:52874692-52874742	HIPEpiC	eye:	n/a
48	chr8:52874692-52874742	GM12891	blood:	n/a
49	chr8:52874692-52874742	H1-hESC	embryonic stem cell:	embryo
50	chr8:52874692-52874742	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:52870845..52873668-chr8:52875256..52877463,2	K562	blood:
2	chr8:52810755..52813318-chr8:52906832..52909651,2	MCF-7	breast:
3	chr8:52870845..52873668-chr8:52875256..52877463,2	K562	blood:
4	chr8:52811794..52813477-chr8:52893629..52895891,2	MCF-7	breast:
5	chr8:52809196..52811979-chr8:52914393..52916351,2	MCF-7	breast:
6	chr8:52897910..52900253-chr8:52910017..52911981,2	MCF-7	breast:
7	chr8:52860243..52863481-chr8:52874076..52876433,3	MCF-7	breast:
8	chr8:52810673..52812861-chr8:52901606..52905084,3	MCF-7	breast:
9	chr8:52897910..52900253-chr8:52910017..52911981,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC090186.1-2	chr8:52888095-52888136	NONHSAT126547
2	lnc-PCMTD1-1	chr8:52908770-52908827	ENSG00000254136
3	lnc-AC090186.1-2	chr8:52874018-52874130	ENSG00000253844
4	lnc-AC090186.1-2	chr8:52886163-52886295	NONHSAT126546

Variant related genes	Relation type
ENSG00000253844	TF binding region
ENSG00000253844	CpG island
ENSG00000272024	chromatin interactions
ENSG00000228801	chromatin interactions
ENSG00000168300	chromatin interactions

Extended variants
information (count: 1566 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1566 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146629822	chr8:52872482-52872483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533671996	chr8:52872515-52872516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141111193	chr8:52872613-52872614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563303114	chr8:52872628-52872629	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs530925620	chr8:52872634-52872635	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs10104454	chr8:52872670-52872671	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs76209356	chr8:52872709-52872710	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs534551941	chr8:52872721-52872722	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs186226446	chr8:52872778-52872779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571501108	chr8:52872781-52872782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116870195	chr8:52872811-52872812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75252179	chr8:52872825-52872826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113627753	chr8:52872826-52872827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1300160	chr8:52872829-52872830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370656877	chr8:52872850-52872851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189909731	chr8:52872851-52872852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182137397	chr8:52872873-52872874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544993213	chr8:52872894-52872895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536230056	chr8:52872898-52872899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554737250	chr8:52872958-52872959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372034964	chr8:52872995-52872996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186497329	chr8:52873039-52873040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145816943	chr8:52873058-52873059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530623172	chr8:52873060-52873061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576253770	chr8:52873075-52873076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541765486	chr8:52873090-52873091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7834181	chr8:52873130-52873131	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572664156	chr8:52873140-52873141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs578192875	chr8:52873190-52873191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545262816	chr8:52873217-52873218	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs191294357	chr8:52873221-52873222	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs149046067	chr8:52873241-52873242	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs116175005	chr8:52873324-52873325	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs143076836	chr8:52873390-52873391	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs78364597	chr8:52873399-52873400	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs7838307	chr8:52873414-52873415	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs372000166	chr8:52873451-52873452	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs369827967	chr8:52873471-52873472	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs533331259	chr8:52873514-52873515	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs138763278	chr8:52873521-52873522	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs117118889	chr8:52873558-52873559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs73681418	chr8:52873578-52873579	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs183530540	chr8:52873649-52873650	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs77334030	chr8:52873650-52873651	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs533843329	chr8:52873734-52873735	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs529347655	chr8:52873840-52873841	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs142689039	chr8:52873846-52873847	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs116867982	chr8:52873855-52873856	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs541030304	chr8:52873904-52873905	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs545174991	chr8:52873929-52873930	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52867000-52873800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:52868200-52873600	Weak transcription	Primary B cells from cord blood	blood
3	chr8:52870200-52874200	Weak transcription	Fetal Brain Male	brain
4	chr8:52870800-52873200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr8:52870800-52873800	Weak transcription	Fetal Muscle Leg	muscle
6	chr8:52871000-52873600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr8:52871000-52874400	Weak transcription	HMEC	breast
8	chr8:52871200-52875000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:52871400-52873800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:52871400-52873800	Weak transcription	Pancreas	Pancrea
11	chr8:52871400-52874200	Weak transcription	Placenta	Placenta
12	chr8:52871400-52874400	Weak transcription	Fetal Intestine Small	intestine
13	chr8:52872200-52873600	Weak transcription	Primary T cells from cord blood	blood
14	chr8:52872400-52872800	Enhancers	Psoas Muscle	Psoas
15	chr8:52872400-52873400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr8:52872400-52873600	Enhancers	GM12878-XiMat	blood
17	chr8:52872600-52872800	Enhancers	Duodenum Mucosa	Duodenum
18	chr8:52872600-52873200	Enhancers	Dnd41	blood
19	chr8:52872600-52874200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr8:52872600-52874200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:52872800-52873800	Weak transcription	Psoas Muscle	Psoas
22	chr8:52872800-52874200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr8:52873000-52874600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr8:52873200-52873800	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr8:52873200-52875600	Flanking Active TSS	Dnd41	blood
26	chr8:52873400-52874400	Enhancers	Primary B cells from peripheral blood	blood
27	chr8:52873600-52873800	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr8:52873600-52873800	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr8:52873600-52874200	Enhancers	Primary T cells from cord blood	blood
30	chr8:52873600-52874200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr8:52873600-52874200	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr8:52873600-52874400	Enhancers	Primary B cells from cord blood	blood
33	chr8:52873600-52874400	Enhancers	Primary T cells fromperipheralblood	blood
34	chr8:52873600-52874400	Enhancers	Primary hematopoietic stem cells	blood
35	chr8:52873600-52874400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr8:52873600-52874400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr8:52873600-52874400	Enhancers	Fetal Thymus	thymus
38	chr8:52873600-52874400	Enhancers	Spleen	Spleen
39	chr8:52873600-52874600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr8:52873600-52874800	Flanking Active TSS	GM12878-XiMat	blood
41	chr8:52873800-52874000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:52873800-52874000	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr8:52873800-52874000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr8:52873800-52874000	Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr8:52873800-52874400	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr8:52873800-52874400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr8:52873800-52874400	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr8:52873800-52874400	Enhancers	Right Atrium	heart
49	chr8:52873800-52874400	Enhancers	Thymus	Thymus
50	chr8:52873800-52874600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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