Variant report

Variant	nsv465752
Chromosome Location	chr8:103953990-103979714
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	ATF2	chr8:103973698-103974445	GM12878	blood:	n/a	n/a
2	BATF	chr8:103973794-103974148	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:103976361-103976593	Hela-S3	cervix:	n/a	chr8:103976486-103976497
4	CEBPB	chr8:103976382-103976664	A549	lung:	n/a	chr8:103976486-103976497
5	CEBPB	chr8:103976354-103976655	IMR90	lung:	n/a	chr8:103976486-103976497
6	CEBPB	chr8:103976353-103976601	HepG2	liver:	n/a	chr8:103976486-103976497
7	CTCF	chr8:103973716-103973904	A549	lung:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
8	CTCF	chr8:103973667-103973887	GM12892	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
9	CTCF	chr8:103973691-103973900	GM19240	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
10	CTCF	chr8:103973700-103973850	GM12878	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
11	CTCF	chr8:103973720-103973870	GM12869	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
12	CTCF	chr8:103973700-103973850	GM12875	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
13	CTCF	chr8:103973739-103973861	HUVEC	blood vessel:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
14	CTCF	chr8:103973729-103973845	MCF-7	breast:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
15	CTCF	chr8:103973720-103973870	GM12865	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
16	CTCF	chr8:103973740-103973890	GM12864	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
17	CTCF	chr8:103973740-103973890	Hela-S3	cervix:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
18	CTCF	chr8:103958095-103958149	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:103973740-103973890	HA-sp	spinal cord:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
20	CTCF	chr8:103973720-103973870	AG09319	gingival:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
21	CTCF	chr8:103973689-103973928	GM12878	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
22	CTCF	chr8:103973720-103973870	HCT-116	colon:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
23	CTCF	chr8:103973700-103973850	HL-60	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
24	CTCF	chr8:103973748-103973845	LNCaP	prostate:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
25	CTCF	chr8:103973700-103973850	HCFaa	heart:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
26	CTCF	chr8:103973500-103973650	HVMF	connective:	n/a	n/a
27	CTCF	chr8:103973700-103973850	BE2_C	brain:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
28	CTCF	chr8:103973740-103973890	HCM	heart:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
29	CTCF	chr8:103973800-103973950	HepG2	liver:	n/a	n/a
30	CTCF	chr8:103973560-103973710	HAc	cerebellar:	n/a	n/a
31	CTCF	chr8:103973700-103973850	HMEC	breast:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
32	CTCF	chr8:103973740-103973890	HPF	lung:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
33	CTCF	chr8:103973675-103973895	H1-hESC	embryonic stem cell:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
34	CTCF	chr8:103973689-103973884	Hela-S3	cervix:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
35	CTCF	chr8:103973710-103973872	GM13977	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
36	CTCF	chr8:103973680-103973830	WERI-Rb-1	eye:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
37	CTCF	chr8:103973649-103973941	IMR90	lung:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
38	CTCF	chr8:103973717-103973843	MCF-7	breast:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
39	CTCF	chr8:103973800-103973950	GM12872	blood:	n/a	n/a
40	CTCF	chr8:103973700-103973850	A549	lung:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
41	CTCF	chr8:103973709-103973867	SK-N-SH_RA	brain:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
42	CTCF	chr8:103973720-103973870	GM12871	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
43	CTCF	chr8:103973700-103973850	HCPEpiC	choroid plexus:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
44	CTCF	chr8:103973740-103973890	GM12873	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
45	CTCF	chr8:103973590-103973976	K562	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
46	CTCF	chr8:103973720-103973870	GM12872	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
47	CTCF	chr8:103973625-103973958	K562	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
48	CTCF	chr8:103973780-103973930	GM12864	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
49	CTCF	chr8:103973740-103973890	BE2_C	brain:	n/a	chr8:103973785-103973798 chr8:103973787-103973795
50	CTCF	chr8:103973700-103973850	GM12866	blood:	n/a	chr8:103973785-103973798 chr8:103973787-103973795

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:103973799-103973849	HL-60	blood:	n/a
2	chr8:103973799-103973849	IMR90	lung:	fetal
3	chr8:103973799-103973849	PANC-1	pancreas:	n/a
4	chr8:103973799-103973849	BJ	skin:	n/a
5	chr8:103973799-103973849	BE2_C	brain:	n/a
6	chr8:103973799-103973849	NH-A	brain:	n/a
7	chr8:103973799-103973849	AG10803	skin:	n/a
8	chr8:103973799-103973849	GM19239	blood:	n/a
9	chr8:103973799-103973849	NHBE	bronchial:	n/a
10	chr8:103973799-103973849	AG04450	lung:	fetal
11	chr8:103973799-103973849	HRPEpiC	eye:	n/a
12	chr8:103973799-103973849	U87	brain:	n/a
13	chr8:103973799-103973849	HEK293	kidney:	embryo
14	chr8:103973799-103973849	HRCEpiC	kidney:	n/a
15	chr8:103973799-103973849	GM06990	blood:	n/a
16	chr8:103973799-103973849	Jurkat	blood:	n/a
17	chr8:103973799-103973849	GM12878	blood:	n/a
18	chr8:103973799-103973849	NB4	blood:	n/a
19	chr8:103973799-103973849	T-47D	breast:	n/a
20	chr8:103973799-103973849	Caco-2	colon:	n/a
21	chr8:103973799-103973849	HCF	heart:	n/a
22	chr8:103973799-103973849	ovcar-3	ovarian:	n/a
23	chr8:103973799-103973849	K562	blood:	n/a
24	chr8:103973799-103973849	SK-N-SH_RA	brain:	n/a
25	chr8:103973799-103973849	HMEC	breast:	n/a
26	chr8:103973799-103973849	H1-hESC	embryonic stem cell:	embryo
27	chr8:103973799-103973849	HNPCEpiC	eye:	n/a
28	chr8:103973799-103973849	HCPEpiC	choroid plexus:	n/a
29	chr8:103973799-103973849	HEEpiC	esophagus:	n/a
30	chr8:103973799-103973849	HCM	heart:	n/a
31	chr8:103973799-103973849	MCF-7	breast:	n/a
32	chr8:103973799-103973849	CMK	blood:	n/a
33	chr8:103973799-103973849	AG09309	skin:	n/a
34	chr8:103973799-103973849	HIPEpiC	eye:	n/a
35	chr8:103973799-103973849	NHDF-neo	bronchial:	n/a
36	chr8:103973799-103973849	LNCaP	prostate:	n/a
37	chr8:103973799-103973849	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:103973799-103973849	GM12892	blood:	n/a
39	chr8:103973799-103973849	SK-N-SH	brain:	n/a
40	chr8:103973799-103973849	Hepatocyte	liver:	n/a
41	chr8:103973799-103973849	HUVEC	blood vessel:	n/a
42	chr8:103973799-103973849	SKMC	muscle:	n/a
43	chr8:103973799-103973849	ECC-1	luminal epithelium:	n/a
44	chr8:103973799-103973849	A549	lung:	n/a
45	chr8:103973799-103973849	AG09319	gingival:	n/a
46	chr8:103973799-103973849	SK-N-MC	brain:	n/a
47	chr8:103973799-103973849	AG04449	skin:	fetal
48	chr8:103973799-103973849	PrEC	prostate:	n/a
49	chr8:103973799-103973849	GM12891	blood:	n/a
50	chr8:103973799-103973849	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:103951762..103954440-chr8:103965375..103967122,2	MCF-7	breast:
2	chr8:103962535..103965315-chr8:103967073..103968689,2	MCF-7	breast:
3	chr8:103964753..103967650-chr8:104045838..104047640,2	K562	blood:
4	chr8:103874529..103876453-chr8:103970493..103973590,3	K562	blood:
5	chr8:103961586..103965372-chr8:103965644..103968506,3	MCF-7	breast:
6	chr8:103874736..103877340-chr8:103957475..103959172,2	MCF-7	breast:
7	chr8:103875368..103877553-chr8:103967686..103969276,3	MCF-7	breast:
8	chr8:103979381..103981672-chr8:103986062..103989018,2	MCF-7	breast:
9	chr8:103875385..103877214-chr8:103958627..103960858,2	MCF-7	breast:
10	chr8:103875112..103879316-chr8:103972204..103974673,4	MCF-7	breast:
11	chr8:103874838..103876433-chr8:103978031..103981018,2	MCF-7	breast:
12	chr8:103977894..103979426-chr8:103982268..103984695,2	MCF-7	breast:
13	chr8:103874330..103878583-chr8:103978201..103983603,5	MCF-7	breast:
14	chr8:103873930..103876740-chr8:103969749..103972556,2	MCF-7	breast:
15	chr8:103937164..103938846-chr8:103972423..103974367,2	MCF-7	breast:
16	chr8:103874782..103876316-chr8:103973931..103975682,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128141
2	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128140
3	lnc-KB-1507C5.2.1-4	chr8:103954149-103955587	NONHSAT128133
4	lnc-KB-1507C5.2.1-4	chr8:103954149-103954193	NONHSAT128119
5	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128139
6	lnc-AZIN1-1	chr8:103966207-103967946	ncRnaDb_ncrna_FR151132_1
7	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT147657
8	lnc-AZIN1-2	chr8:103954149-103954281	NONHSAT128138
9	lnc-AZIN1-2	chr8:103961693-103962042	NONHSAT128138
10	lnc-KB-1507C5.2.1-4	chr8:103961299-103961462	l_3661_chr8:103945582-103948344_thyroid
11	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128132
12	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128134
13	lnc-ATP6V1C1-6	chr8:103976074-103976692	ncRnaDb_ncrna_FR026950_1

Variant related genes	Relation type
ENSG00000201216	TF binding region
ENSG00000265898	TF binding region
ENSG00000201216	CpG island
ENSG00000265898	CpG island
ENSG00000253320	chromatin interactions
ENSG00000201216	chromatin interactions
ENSG00000155096	chromatin interactions

Extended variants
information (count: 1015 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs651816	chr8:103953990-103953991	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572064584	chr8:103954058-103954059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144654259	chr8:103954065-103954066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2458278	chr8:103954081-103954082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373586400	chr8:103954091-103954092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547135745	chr8:103954109-103954110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571989828	chr8:103954162-103954163	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs368645287	chr8:103954171-103954172	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs539314897	chr8:103954175-103954176	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs7821253	chr8:103954240-103954241	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs76594553	chr8:103954270-103954271	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs144286576	chr8:103954276-103954277	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs575646223	chr8:103954363-103954364	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs573246519	chr8:103954376-103954377	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs534535381	chr8:103954421-103954422	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs553106107	chr8:103954429-103954430	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs577544486	chr8:103954440-103954441	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs550063968	chr8:103954456-103954457	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs113736280	chr8:103954463-103954464	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs192649038	chr8:103954467-103954468	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs146588376	chr8:103954499-103954500	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs542565731	chr8:103954516-103954517	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs560831553	chr8:103954543-103954544	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs374331399	chr8:103954581-103954582	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs546904348	chr8:103954637-103954638	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
26	rs114767204	chr8:103954680-103954681	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
27	rs111323791	chr8:103954706-103954707	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
28	rs371404379	chr8:103954709-103954710	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
29	rs62526543	chr8:103954714-103954715	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
30	rs368381829	chr8:103954744-103954745	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
31	rs13262022	chr8:103954754-103954755	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
32	rs62526544	chr8:103954757-103954758	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
33	rs112859472	chr8:103954762-103954763	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
34	rs71506356	chr8:103954764-103954765	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
35	rs549609	chr8:103954805-103954806	Weak transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs71276499	chr8:103954806-103954807	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
37	rs116582607	chr8:103954813-103954814	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
38	rs376263870	chr8:103954854-103954855	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
39	rs536257892	chr8:103954869-103954870	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
40	rs35644318	chr8:103954877-103954878	Weak transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs2513890	chr8:103954925-103954926	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
42	rs58159579	chr8:103954975-103954976	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
43	rs372279364	chr8:103954976-103954977	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
44	rs374126113	chr8:103954978-103954979	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
45	rs566874906	chr8:103954979-103954980	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
46	rs534279226	chr8:103954994-103954995	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
47	rs150985713	chr8:103954997-103954998	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
48	rs577406806	chr8:103955004-103955005	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs2513889	chr8:103955029-103955030	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs2513888	chr8:103955036-103955037	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
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
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
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
Multiple myeloma	16461302	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
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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103932200-103959400	Weak transcription	Fetal Brain Female	brain
2	chr8:103937800-103956000	Weak transcription	Brain Hippocampus Middle	brain
3	chr8:103940200-103972600	Weak transcription	Ovary	ovary
4	chr8:103943800-103973600	Weak transcription	Fetal Kidney	kidney
5	chr8:103945400-103956800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr8:103946800-103974000	Weak transcription	Brain Germinal Matrix	brain
7	chr8:103947600-103963400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr8:103948600-103957200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:103948800-103956800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr8:103950400-103961000	Weak transcription	Pancreas	Pancrea
11	chr8:103952400-103957600	Weak transcription	Fetal Intestine Small	intestine
12	chr8:103952600-103954600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:103952600-103973600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr8:103952800-103958200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr8:103952800-103971000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr8:103953000-103967200	Weak transcription	Brain Substantia Nigra	brain
17	chr8:103953000-103968800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr8:103953200-103972800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr8:103953200-103974000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:103953400-103954000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:103953600-103958400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr8:103953600-103973400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:103953800-103958200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr8:103953800-103958200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr8:103953800-103958400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr8:103954000-103962400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr8:103954200-103956800	Weak transcription	Fetal Stomach	stomach
28	chr8:103954600-103955000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
29	chr8:103955000-103961000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr8:103956800-103957000	Enhancers	Fetal Muscle Trunk	muscle
31	chr8:103957000-103957800	Weak transcription	Fetal Muscle Trunk	muscle
32	chr8:103957600-103958200	Strong transcription	Fetal Intestine Small	intestine
33	chr8:103957800-103958200	Enhancers	Fetal Muscle Trunk	muscle
34	chr8:103958000-103958400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr8:103958200-103958600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr8:103958200-103958600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:103958200-103958600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr8:103958200-103958600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr8:103958200-103958600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:103958200-103958600	Enhancers	HSMM	muscle
41	chr8:103958200-103958800	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr8:103958200-103959000	Enhancers	HSMMtube	muscle
43	chr8:103958200-103959800	Weak transcription	Fetal Intestine Small	intestine
44	chr8:103958400-103958600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr8:103958400-103959000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr8:103959000-103973400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr8:103961000-103961200	Strong transcription	Pancreas	Pancrea
48	chr8:103961000-103961600	Strong transcription	H9 Cell Line	embryonic stem cell
49	chr8:103961200-103961400	Genic enhancers	Pancreas	Pancrea
50	chr8:103961400-103961600	Strong transcription	Pancreas	Pancrea

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