Variant report

Variant	nsv831384
Chromosome Location	chr8:88746718-88917248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:518)
CpG islands
(count:1100)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:88893430-88893620	K562	blood:	n/a	n/a
2	ATF1	chr8:88886163-88886450	K562	blood:	n/a	n/a
3	ATF1	chr8:88823819-88824074	K562	blood:	n/a	n/a
4	BACH1	chr8:88793459-88793553	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:88885154-88885612	K562	blood:	n/a	n/a
6	BHLHE40	chr8:88886230-88886430	K562	blood:	n/a	n/a
7	CBX3	chr8:88886060-88886543	K562	blood:	n/a	n/a
8	CBX3	chr8:88886148-88886472	K562	blood:	n/a	n/a
9	CEBPB	chr8:88844381-88845171	H1-hESC	embryonic stem cell:	n/a	chr8:88844663-88844674
10	CEBPB	chr8:88905282-88905596	HepG2	liver:	n/a	chr8:88905455-88905466
11	CEBPB	chr8:88881550-88881750	K562	blood:	n/a	chr8:88881626-88881637
12	CEBPB	chr8:88844457-88845101	K562	blood:	n/a	chr8:88844663-88844674
13	CEBPB	chr8:88844407-88845130	Hela-S3	cervix:	n/a	chr8:88844663-88844674
14	CEBPB	chr8:88881537-88881766	HepG2	liver:	n/a	chr8:88881626-88881637
15	CEBPB	chr8:88844476-88845180	A549	lung:	n/a	chr8:88844663-88844674
16	CEBPB	chr8:88905294-88905601	IMR90	lung:	n/a	chr8:88905455-88905466
17	CEBPB	chr8:88888876-88889065	A549	lung:	n/a	chr8:88888968-88888981 chr8:88888968-88888979 chr8:88888968-88888981 chr8:88888968-88888981 chr8:88888965-88888982
18	CEBPB	chr8:88844423-88844796	A549	lung:	n/a	chr8:88844663-88844674
19	CEBPB	chr8:88914854-88914986	K562	blood:	n/a	chr8:88914891-88914902
20	CEBPB	chr8:88888854-88889128	HepG2	liver:	n/a	chr8:88888968-88888981 chr8:88888968-88888979 chr8:88888968-88888981 chr8:88888968-88888981 chr8:88888965-88888982
21	CEBPB	chr8:88844451-88844800	ECC-1	luminal epithelium:	n/a	chr8:88844663-88844674
22	CEBPB	chr8:88776700-88776957	H1-hESC	embryonic stem cell:	n/a	chr8:88776818-88776829
23	CEBPB	chr8:88763797-88763933	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr8:88844275-88845108	MCF-7	breast:	n/a	chr8:88844663-88844674
25	CEBPB	chr8:88917060-88917510	MCF-7	breast:	n/a	n/a
26	CEBPB	chr8:88904327-88904586	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:88917172-88917445	K562	blood:	n/a	n/a
28	CEBPB	chr8:88911974-88912386	MCF-7	breast:	n/a	n/a
29	CEBPB	chr8:88914798-88915018	HepG2	liver:	n/a	chr8:88914891-88914902
30	CEBPB	chr8:88905319-88905558	Hela-S3	cervix:	n/a	chr8:88905455-88905466
31	CEBPB	chr8:88844270-88844984	HCT-116	colon:	n/a	chr8:88844663-88844674
32	CEBPB	chr8:88844482-88845032	HepG2	liver:	n/a	chr8:88844663-88844674
33	CEBPB	chr8:88914714-88915044	IMR90	lung:	n/a	chr8:88914891-88914902
34	CEBPB	chr8:88881495-88881763	H1-hESC	embryonic stem cell:	n/a	chr8:88881626-88881637
35	CEBPB	chr8:88917148-88917387	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr8:88912052-88912299	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:88914784-88915005	A549	lung:	n/a	chr8:88914891-88914902
38	CEBPB	chr8:88917124-88917445	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:88844390-88845179	IMR90	lung:	n/a	chr8:88844663-88844674
40	CEBPB	chr8:88905306-88905587	A549	lung:	n/a	chr8:88905455-88905466
41	CEBPB	chr8:88904429-88904580	K562	blood:	n/a	n/a
42	CEBPB	chr8:88904275-88904691	MCF-7	breast:	n/a	n/a
43	CHD2	chr8:88885216-88885334	K562	blood:	n/a	n/a
44	CHD2	chr8:88886202-88886586	K562	blood:	n/a	n/a
45	CHD2	chr8:88844855-88845050	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr8:88844460-88844610	HMF	breast:	n/a	n/a
47	CTCF	chr8:88844442-88844611	LNCaP	prostate:	n/a	n/a
48	CTCF	chr8:88844420-88844570	WI-38	lung:	n/a	n/a
49	CTCF	chr8:88844370-88844647	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:88856940-88857090	HPAF	blood vessel:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:88760082-88760132	HRE	kidney:	n/a
2	chr8:88885186-88885236	NHBE	bronchial:	n/a
3	chr8:88760082-88760132	HRE	kidney:	n/a
4	chr8:88885186-88885236	NHBE	bronchial:	n/a
5	chr8:88886320-88886370	A549	lung:	n/a
6	chr8:88886262-88886312	NH-A	brain:	n/a
7	chr8:88886051-88886101	NB4	blood:	n/a
8	chr8:88886339-88886389	Hepatocyte	liver:	n/a
9	chr8:88886262-88886312	HRPEpiC	eye:	n/a
10	chr8:88889648-88889698	AG09319	gingival:	n/a
11	chr8:88760082-88760132	BJ	skin:	n/a
12	chr8:88884985-88885035	HCT-116	colon:	n/a
13	chr8:88886320-88886370	MCF-7	breast:	n/a
14	chr8:88886432-88886482	HAEpiC	amniotic membrane:	n/a
15	chr8:88889648-88889698	AG10803	skin:	n/a
16	chr8:88885254-88885304	K562	blood:	n/a
17	chr8:88886320-88886370	HCPEpiC	choroid plexus:	n/a
18	chr8:88885469-88885519	HEEpiC	esophagus:	n/a
19	chr8:88889648-88889698	GM12892	blood:	n/a
20	chr8:88885186-88885236	HRPEpiC	eye:	n/a
21	chr8:88845118-88845168	HepG2	liver:	n/a
22	chr8:88886411-88886461	AG09309	skin:	n/a
23	chr8:88886301-88886351	HCT-116	colon:	n/a
24	chr8:88845118-88845168	PANC-1	pancreas:	n/a
25	chr8:88886262-88886312	HAEpiC	amniotic membrane:	n/a
26	chr8:88886320-88886370	IMR90	lung:	fetal
27	chr8:88886306-88886356	ProgFib	skin:	n/a
28	chr8:88886306-88886356	H1-hESC	embryonic stem cell:	embryo
29	chr8:88885254-88885304	PANC-1	pancreas:	n/a
30	chr8:88886262-88886312	SK-N-SH_RA	brain:	n/a
31	chr8:88885186-88885236	GM12891	blood:	n/a
32	chr8:88886301-88886351	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:88885043-88885093	HUVEC	blood vessel:	n/a
34	chr8:88886320-88886370	NT2-D1	testis:	n/a
35	chr8:88886301-88886351	SK-N-SH	brain:	n/a
36	chr8:88886301-88886351	HMEC	breast:	n/a
37	chr8:88889648-88889698	HCM	heart:	n/a
38	chr8:88884156-88884206	NT2-D1	testis:	n/a
39	chr8:88886411-88886461	HRE	kidney:	n/a
40	chr8:88845118-88845168	GM19239	blood:	n/a
41	chr8:88886320-88886370	CMK	blood:	n/a
42	chr8:88886432-88886482	HEK293	kidney:	embryo
43	chr8:88885043-88885093	ECC-1	luminal epithelium:	n/a
44	chr8:88886339-88886389	HCF	heart:	n/a
45	chr8:88889648-88889698	LNCaP	prostate:	n/a
46	chr8:88886432-88886482	HCPEpiC	choroid plexus:	n/a
47	chr8:88845118-88845168	HRCEpiC	kidney:	n/a
48	chr8:88884156-88884206	AG04450	lung:	fetal
49	chr8:88884985-88885035	GM06990	blood:	n/a
50	chr8:88886306-88886356	SKMC	muscle:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:88879930..88882837-chr8:88894807..88896983,2	MCF-7	breast:
2	chr8:88844099..88844976-chr8:89566466..89567055,2	MCF-7	breast:
3	chr8:88843989..88844789-chr8:89301629..89302601,7	MCF-7	breast:
4	chr8:88883093..88885069-chr8:89007816..89009519,2	MCF-7	breast:
5	chr8:88844020..88845021-chr8:89301693..89302582,7	MCF-7	breast:
6	chr8:88837049..88839934-chr8:88843106..88844697,2	MCF-7	breast:
7	chr8:88837817..88839528-chr8:88842838..88844637,2	MCF-7	breast:
8	chr8:88843768..88844920-chr8:89332543..89333442,5	MCF-7	breast:
9	chr8:88910926..88912766-chr8:88929269..88932098,2	MCF-7	breast:
10	chr8:88752001..88754722-chr8:88761392..88764098,2	MCF-7	breast:
11	chr8:88844023..88845076-chr8:89068948..89070439,5	MCF-7	breast:
12	chr8:88837049..88839934-chr8:88843106..88844697,2	MCF-7	breast:
13	chr8:88874875..88877431-chr8:88884154..88886402,2	K562	blood:
14	chr2:123589396..123591482-chr8:88778600..88780103,2	MCF-7	breast:
15	chr8:88771464..88773201-chr8:88775160..88777510,2	MCF-7	breast:
16	chr8:88771464..88773201-chr8:88775160..88777510,2	MCF-7	breast:
17	chr8:88594302..88595226-chr8:88844378..88845025,3	MCF-7	breast:
18	chr8:88752001..88754722-chr8:88761392..88764098,2	MCF-7	breast:
19	chr8:88837817..88839528-chr8:88842838..88844637,2	MCF-7	breast:
20	chr8:88879930..88882837-chr8:88894807..88896983,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCAF4L2-2	chr8:88763435-88763545	ENSG00000253500.1
2	lnc-DCAF4L2-2	chr8:88767880-88767946	ENSG00000253500.1
3	lnc-DCAF4L2-2	chr8:88767880-88767923	ENSG00000253500.1
4	lnc-DCAF4L2-2	chr8:88763435-88763545	ENSG00000253500.1

No data

Variant related genes	Relation type
ENSG00000253500	TF binding region
DCAF4L2	TF binding region
SOX5P	TF binding region
ENSG00000253500	CpG island
DCAF4L2	CpG island
SOX5P	CpG island
ENSG00000176566	chromatin interactions

Extended variants
information (count: 1876 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1876 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574226445	chr8:88748771-88748772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs368302595	chr8:88748921-88748922	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs541500567	chr8:88748933-88748934	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563157696	chr8:88748947-88748948	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs545832856	chr8:88749710-88749711	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs564064409	chr8:88749721-88749722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs202139057	chr8:88749728-88749729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs573210342	chr8:88749729-88749730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs540513081	chr8:88749738-88749739	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs577382021	chr8:88759600-88759601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538756371	chr8:88759655-88759656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570204767	chr8:88759694-88759695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7827917	chr8:88759706-88759707	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs373914587	chr8:88759726-88759727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530452130	chr8:88759756-88759757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141765445	chr8:88759768-88759769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542697630	chr8:88759785-88759786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561320567	chr8:88759836-88759837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13439375	chr8:88759846-88759847	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs544103199	chr8:88759870-88759871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570471162	chr8:88759907-88759908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12549708	chr8:88759973-88759974	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs75333536	chr8:88759981-88759982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532714800	chr8:88759991-88759992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551505982	chr8:88760034-88760035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560028881	chr8:88760056-88760057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs13256471	chr8:88760083-88760084	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs548728161	chr8:88760167-88760168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs12549752	chr8:88760185-88760186	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs146253687	chr8:88760262-88760263	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs141203424	chr8:88760276-88760277	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181390537	chr8:88760287-88760288	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs538493903	chr8:88760361-88760362	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs555512035	chr8:88760389-88760390	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs117391161	chr8:88760459-88760460	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs536729109	chr8:88760497-88760498	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs116614360	chr8:88760502-88760503	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs576353350	chr8:88760523-88760524	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs72673112	chr8:88760576-88760577	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs559249572	chr8:88760598-88760599	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs577601108	chr8:88760643-88760644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186903036	chr8:88760704-88760705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559873397	chr8:88760737-88760738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527414174	chr8:88760750-88760751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190700714	chr8:88760756-88760757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574273682	chr8:88760809-88760810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535688634	chr8:88760866-88760867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377521960	chr8:88760925-88760926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531162231	chr8:88760934-88760935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549361366	chr8:88760946-88760947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:88759600-88760200	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr8:88759600-88761200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr8:88759800-88760000	Enhancers	H1 Cell Line	embryonic stem cell
4	chr8:88759800-88760000	Enhancers	H9 Cell Line	embryonic stem cell
5	chr8:88759800-88760000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:88759800-88760000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:88759800-88760000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:88759800-88760600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:88759800-88760800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr8:88760000-88763000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr8:88760000-88766200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:88760000-88768000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr8:88760000-88770600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr8:88760200-88760600	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr8:88760200-88760800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr8:88762400-88763200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr8:88762600-88765200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:88763000-88763600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr8:88763200-88763400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
20	chr8:88763400-88765000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr8:88764800-88765000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr8:88766000-88766600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr8:88766200-88766400	Enhancers	H9 Cell Line	embryonic stem cell
24	chr8:88766200-88766400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:88766200-88766600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr8:88766400-88767400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:88768000-88768200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
28	chr8:88769200-88769600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
29	chr8:88769600-88771000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr8:88771400-88772000	Enhancers	Fetal Brain Male	brain
31	chr8:88771800-88772200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:88788400-88790200	Enhancers	HUVEC	blood vessel
33	chr8:88790200-88791200	ZNF genes & repeats	Aorta	Aorta
34	chr8:88790800-88791000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:88790800-88791200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:88796800-88798200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
37	chr8:88797400-88797800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr8:88825400-88826600	Enhancers	Fetal Brain Male	brain
39	chr8:88838200-88838600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:88838200-88839200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr8:88838200-88839200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr8:88838200-88840000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:88838600-88839200	Enhancers	Primary hematopoietic stem cells	blood
44	chr8:88838600-88839200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:88838800-88839200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:88839200-88839600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr8:88839200-88843800	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr8:88839200-88844200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr8:88839600-88843800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:88840000-88844200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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