Variant report

Variant	nsv962456
Chromosome Location	chr17:45163689-45212872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:707)
CpG islands
(count:612)
Chromatin interactive
region (count:25)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45178080-45178088	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:45191135-45191603	K562	blood:	n/a	n/a
3	ARID3A	chr17:45165062-45165080	K562	blood:	n/a	n/a
4	ATF1	chr17:45212762-45214888	K562	blood:	n/a	n/a
5	ATF1	chr17:45176347-45176414	K562	blood:	n/a	n/a
6	ATF3	chr17:45212743-45214880	K562	blood:	n/a	n/a
7	BACH1	chr17:45177408-45177655	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr17:45191283-45191331	K562	blood:	n/a	n/a
9	BACH1	chr17:45212712-45214898	K562	blood:	n/a	n/a
10	BCL3	chr17:45212826-45213264	GM12878	blood:	n/a	n/a
11	BCL3	chr17:45177585-45178094	A549	lung:	n/a	n/a
12	BCLAF1	chr17:45177412-45177731	GM12878	blood:	n/a	n/a
13	BDP1	chr17:45212734-45214890	K562	blood:	n/a	n/a
14	BHLHE40	chr17:45177528-45177799	GM12878	blood:	n/a	n/a
15	BHLHE40	chr17:45177425-45177752	K562	blood:	n/a	n/a
16	BHLHE40	chr17:45176199-45176524	GM12878	blood:	n/a	n/a
17	BHLHE40	chr17:45176257-45176572	K562	blood:	n/a	n/a
18	BRCA1	chr17:45177718-45177810	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr17:45212726-45214898	GM12878	blood:	n/a	n/a
20	BRCA1	chr17:45212742-45214897	Hela-S3	cervix:	n/a	n/a
21	BRF1	chr17:45212753-45214897	K562	blood:	n/a	n/a
22	BRF2	chr17:45212730-45214887	K562	blood:	n/a	n/a
23	BRF2	chr17:45212732-45214887	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr17:45176116-45176464	K562	blood:	n/a	n/a
25	CBX3	chr17:45183455-45183828	K562	blood:	n/a	n/a
26	CCNT2	chr17:45177380-45177744	K562	blood:	n/a	chr17:45177652-45177661
27	CEBPB	chr17:45179693-45179787	HepG2	liver:	n/a	chr17:45179737-45179748
28	CEBPB	chr17:45186544-45187072	A549	lung:	n/a	chr17:45186889-45186900
29	CEBPB	chr17:45186765-45187032	Hela-S3	cervix:	n/a	chr17:45186889-45186900
30	CEBPB	chr17:45186716-45187064	K562	blood:	n/a	chr17:45186889-45186900
31	CEBPB	chr17:45179721-45179888	A549	lung:	n/a	chr17:45179737-45179748
32	CEBPB	chr17:45186740-45186992	A549	lung:	n/a	chr17:45186889-45186900
33	CEBPB	chr17:45186735-45187052	HepG2	liver:	n/a	chr17:45186889-45186900
34	CEBPD	chr17:45183555-45183952	K562	blood:	n/a	n/a
35	CEBPD	chr17:45177335-45177879	HepG2	liver:	n/a	n/a
36	CEBPZ	chr17:45177620-45177795	HepG2	liver:	n/a	n/a
37	CHD1	chr17:45177363-45177588	GM12878	blood:	n/a	n/a
38	CHD2	chr17:45177434-45177950	GM12878	blood:	n/a	n/a
39	CHD2	chr17:45177530-45177902	K562	blood:	n/a	n/a
40	CHD2	chr17:45177505-45177823	HepG2	liver:	n/a	n/a
41	CHD2	chr17:45177441-45177829	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr17:45177396-45177943	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr17:45177555-45177825	A549	lung:	n/a	n/a
44	CREB1	chr17:45177184-45177885	A549	lung:	n/a	n/a
45	CREB1	chr17:45177262-45177977	HepG2	liver:	n/a	n/a
46	CTCF	chr17:45177440-45177590	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr17:45177420-45177570	GM12878	blood:	n/a	n/a
48	CTCF	chr17:45192967-45193078	GM10248	blood:	n/a	n/a
49	CTCF	chr17:45177460-45177610	GM12871	blood:	n/a	n/a
50	CTCF	chr17:45177440-45177590	WERI-Rb-1	eye:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45177429-45177479	MCF-7	breast:	n/a
2	chr17:45177628-45177678	SAEC	small airway:	n/a
3	chr17:45177429-45177479	MCF-7	breast:	n/a
4	chr17:45177628-45177678	SAEC	small airway:	n/a
5	chr17:45177628-45177678	Hela-S3	cervix:	n/a
6	chr17:45198207-45198257	HUVEC	blood vessel:	n/a
7	chr17:45177431-45177481	HRCEpiC	kidney:	n/a
8	chr17:45177598-45177648	GM12878	blood:	n/a
9	chr17:45177431-45177481	Hepatocyte	liver:	n/a
10	chr17:45177598-45177648	HRE	kidney:	n/a
11	chr17:45177431-45177481	SK-N-SH_RA	brain:	n/a
12	chr17:45177628-45177678	PrEC	prostate:	n/a
13	chr17:45177431-45177481	SKMC	muscle:	n/a
14	chr17:45177429-45177479	HNPCEpiC	eye:	n/a
15	chr17:45177859-45177909	HPAEpiC	pulmonary alveolar:	n/a
16	chr17:45177378-45177428	MCF10A-Er-Src	breast:	n/a
17	chr17:45180460-45180510	GM12878	blood:	n/a
18	chr17:45198207-45198257	PFSK-1	brain:	n/a
19	chr17:45177859-45177909	ProgFib	skin:	n/a
20	chr17:45177378-45177428	BE2_C	brain:	n/a
21	chr17:45177859-45177909	ovcar-3	ovarian:	n/a
22	chr17:45177628-45177678	HRE	kidney:	n/a
23	chr17:45177431-45177481	T-47D	breast:	n/a
24	chr17:45174155-45174205	PFSK-1	brain:	n/a
25	chr17:45177859-45177909	NT2-D1	testis:	n/a
26	chr17:45183984-45184034	PFSK-1	brain:	n/a
27	chr17:45183984-45184034	GM06990	blood:	n/a
28	chr17:45177431-45177481	SAEC	small airway:	n/a
29	chr17:45180460-45180510	SK-N-SH_RA	brain:	n/a
30	chr17:45183984-45184034	AG09319	gingival:	n/a
31	chr17:45177598-45177648	MCF-7	breast:	n/a
32	chr17:45177628-45177678	HepG2	liver:	n/a
33	chr17:45183984-45184034	HEEpiC	esophagus:	n/a
34	chr17:45174155-45174205	HRPEpiC	eye:	n/a
35	chr17:45177628-45177678	NH-A	brain:	n/a
36	chr17:45174155-45174205	ovcar-3	ovarian:	n/a
37	chr17:45177598-45177648	HEEpiC	esophagus:	n/a
38	chr17:45183984-45184034	MCF10A-Er-Src	breast:	n/a
39	chr17:45177598-45177648	HL-60	blood:	n/a
40	chr17:45174155-45174205	BJ	skin:	n/a
41	chr17:45177598-45177648	BE2_C	brain:	n/a
42	chr17:45174155-45174205	AG04450	lung:	fetal
43	chr17:45174155-45174205	SK-N-MC	brain:	n/a
44	chr17:45177378-45177428	SK-N-MC	brain:	n/a
45	chr17:45183984-45184034	HCT-116	colon:	n/a
46	chr17:45177598-45177648	HRPEpiC	eye:	n/a
47	chr17:45180460-45180510	HRCEpiC	kidney:	n/a
48	chr17:45177431-45177481	GM12878	blood:	n/a
49	chr17:45177429-45177479	HIPEpiC	eye:	n/a
50	chr17:45177598-45177648	IMR90	lung:	fetal

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45169541..45171629-chr17:45172586..45174850,2	K562	blood:
2	chr17:45143258..45146165-chr17:45178013..45180632,2	K562	blood:
3	chr17:45195494..45197087-chr17:45199093..45201965,2	K562	blood:
4	chr17:45170129..45171669-chr17:45173350..45174934,2	K562	blood:
5	chr17:45190584..45193064-chr17:45401116..45402656,2	K562	blood:
6	chr17:44302347..44303352-chr17:45177408..45178065,4	HCT-116	colon:
7	chr17:45162074..45163604-chr17:45171046..45173992,2	MCF-7	breast:
8	chr17:45155821..45158287-chr17:45163734..45167832,3	K562	blood:
9	chr17:45179866..45182150-chr17:45185203..45188192,2	K562	blood:
10	chr17:45159211..45163683-chr17:45163741..45168313,5	K562	blood:
11	chr17:45179866..45182150-chr17:45185203..45188192,2	K562	blood:
12	chr17:45156502..45159050-chr17:45162212..45165184,2	K562	blood:
13	chr17:45195494..45197087-chr17:45199093..45201965,2	K562	blood:
14	chr17:45143436..45146346-chr17:45178059..45181405,3	K562	blood:
15	chr17:45163760..45166072-chr17:45166357..45168655,2	K562	blood:
16	chr17:45170129..45171669-chr17:45173350..45174934,2	K562	blood:
17	chr17:45207192..45209453-chr17:45214341..45217324,3	K562	blood:
18	chr17:45207790..45209318-chr17:45237237..45238826,2	K562	blood:
19	chr17:45163760..45166072-chr17:45166357..45168655,2	K562	blood:
20	chr17:45201166..45202971-chr17:45204243..45206513,3	K562	blood:
21	chr17:45201166..45204162-chr17:45204579..45207992,3	K562	blood:
22	chr17:45169541..45171629-chr17:45172586..45174850,2	K562	blood:
23	chr17:45177573..45179138-chr17:45179846..45181452,2	MCF-7	breast:
24	chr17:45211653..45214560-chr17:45231641..45234372,2	MCF-7	breast:
25	chr17:45145658..45148463-chr17:45161187..45163786,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPRML-3	chr17:45177201-45177614	ENSG00000262879.1
2	lnc-MYL4-2	chr17:45212171-45213246	ENSG00000249938
3	lnc-RPRML-3	chr17:45176744-45177617	NONHSAT054281
4	lnc-RPRML-3	chr17:45177201-45177614	NONHSAT054277
5	lnc-RPRML-3	chr17:45177201-45177605	ENSG00000262879.1
6	lnc-RPRML-3	chr17:45177201-45177560	NONHSAT054278
7	lnc-RPRML-3	chr17:45177201-45177631	NONHSAT054279

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CDC27	hsa-miR-32-5p	chr17:45198125-45198146
2	CDC27	hsa-miR-16-5p	chr17:45195640-45195634
3	CDC27	hsa-miR-16-5p	chr17:45195634-45195658
4	CDC27	hsa-miR-32-5p	chr17:45198131-45198124

Variant related genes	Relation type
CDC27	TF binding region
ENSG00000221016	TF binding region
ENSG00000262879	TF binding region
CDC27	CpG island
ENSG00000221016	CpG island
ENSG00000262879	CpG island
ENSG00000239291	chromatin interactions
ENSG00000120071	chromatin interactions
ENSG00000262879	chromatin interactions
ENSG00000221016	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000004897	chromatin interactions
BCCIP	miRNA target sites

Extended variants
information (count: 1887 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1887 , 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	rs114929350	chr17:45163696-45163697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376821687	chr17:45163717-45163718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550984917	chr17:45163723-45163724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148958749	chr17:45163736-45163737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143640030	chr17:45163745-45163746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547280186	chr17:45163755-45163756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138307390	chr17:45163758-45163759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs71365036	chr17:45163817-45163818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371531677	chr17:45163818-45163819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs386386173	chr17:45163841-45163842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10686268	chr17:45163842-45163843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs62074462	chr17:45163845-45163846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375876362	chr17:45163855-45163856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143724017	chr17:45163856-45163857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371696801	chr17:45163857-45163858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369889486	chr17:45163905-45163906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536788632	chr17:45163916-45163917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556639068	chr17:45163920-45163921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563632416	chr17:45163945-45163946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535655965	chr17:45164027-45164028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556913019	chr17:45164042-45164043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9899078	chr17:45164056-45164057	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs545747630	chr17:45164071-45164072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559624456	chr17:45164087-45164088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189480333	chr17:45164146-45164147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573203864	chr17:45164174-45164175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552173640	chr17:45164238-45164239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561906284	chr17:45164265-45164266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545827286	chr17:45164273-45164274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374835831	chr17:45164365-45164366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150542177	chr17:45164366-45164367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370612647	chr17:45164367-45164368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531024211	chr17:45164390-45164391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181480381	chr17:45164403-45164404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564281887	chr17:45164409-45164410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533378621	chr17:45164443-45164444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374708451	chr17:45164497-45164498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546949351	chr17:45164532-45164533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567129275	chr17:45164550-45164551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572903787	chr17:45164582-45164583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186263090	chr17:45164589-45164590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138808729	chr17:45164707-45164708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569114226	chr17:45164712-45164713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528609511	chr17:45164741-45164742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557037179	chr17:45164786-45164787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191419014	chr17:45164787-45164788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369282704	chr17:45164811-45164812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181394581	chr17:45164911-45164912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552729238	chr17:45164925-45164926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186615587	chr17:45164936-45164937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1388 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45145000-45163800	Weak transcription	Small Intestine	intestine
2	chr17:45145000-45164600	Weak transcription	Brain Angular Gyrus	brain
3	chr17:45145000-45169800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr17:45145000-45169800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr17:45145000-45169800	Weak transcription	Fetal Lung	lung
6	chr17:45145000-45176400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr17:45145000-45176600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr17:45145000-45176800	Weak transcription	Lung	lung
9	chr17:45145200-45169200	Weak transcription	Primary B cells from cord blood	blood
10	chr17:45145200-45170200	Weak transcription	Brain Germinal Matrix	brain
11	chr17:45145200-45176600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr17:45145400-45176000	Weak transcription	Primary T cells from cord blood	blood
13	chr17:45146400-45169800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr17:45146400-45170800	Weak transcription	Dnd41	blood
15	chr17:45148800-45175400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr17:45149000-45164200	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr17:45149000-45168600	Weak transcription	Primary B cells from peripheral blood	blood
18	chr17:45149000-45170000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr17:45149000-45173800	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr17:45149600-45175400	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr17:45149600-45176800	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr17:45150200-45170000	Weak transcription	Ovary	ovary
23	chr17:45150200-45174600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr17:45150600-45164600	Weak transcription	Brain Anterior Caudate	brain
25	chr17:45150600-45167200	Weak transcription	Spleen	Spleen
26	chr17:45150600-45169800	Weak transcription	Fetal Muscle Leg	muscle
27	chr17:45150600-45170600	Weak transcription	HSMM	muscle
28	chr17:45150600-45176400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr17:45150600-45176800	Weak transcription	Left Ventricle	heart
30	chr17:45155000-45169800	Weak transcription	Fetal Brain Female	brain
31	chr17:45155600-45170200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr17:45155600-45170200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr17:45155600-45170200	Weak transcription	NHEK	skin
34	chr17:45155600-45173600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr17:45158200-45170600	Weak transcription	A549	lung
36	chr17:45158600-45169800	Weak transcription	Fetal Thymus	thymus
37	chr17:45158600-45175000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr17:45159200-45175600	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr17:45159600-45169800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr17:45159800-45169800	Weak transcription	Fetal Stomach	stomach
41	chr17:45159800-45170200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr17:45161200-45164400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr17:45162200-45163800	Enhancers	HepG2	liver
44	chr17:45162200-45164200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr17:45162400-45163800	Enhancers	Fetal Intestine Small	intestine
46	chr17:45162400-45164200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr17:45162600-45170000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr17:45162800-45164800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr17:45163000-45163800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr17:45163200-45164400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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