Variant report

Variant	nsv888835
Chromosome Location	chr7:102103293-102110890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:938)
CpG islands
(count:979)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102105026-102105477	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102107670-102107707	HepG2	liver:	n/a	n/a
3	ATF2	chr7:102105214-102105642	GM12878	blood:	n/a	n/a
4	ATF3	chr7:102105121-102105483	H1-hESC	embryonic stem cell:	n/a	chr7:102105134-102105143
5	ATF3	chr7:102105079-102105666	K562	blood:	n/a	chr7:102105134-102105143
6	ATF3	chr7:102105156-102105479	HepG2	liver:	n/a	n/a
7	ATF3	chr7:102105052-102105541	A549	lung:	n/a	chr7:102105134-102105143
8	BACH1	chr7:102105195-102105583	K562	blood:	n/a	n/a
9	BACH1	chr7:102105152-102105627	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:102106969-102107235	GM12878	blood:	n/a	chr7:102107141-102107152
11	BCL3	chr7:102105600-102105954	A549	lung:	n/a	n/a
12	BCL3	chr7:102104786-102105505	A549	lung:	n/a	n/a
13	BCLAF1	chr7:102105007-102105737	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:102105109-102105696	K562	blood:	n/a	n/a
15	BHLHE40	chr7:102104315-102104322	K562	blood:	n/a	n/a
16	BHLHE40	chr7:102105053-102105547	GM12878	blood:	n/a	chr7:102105343-102105359 chr7:102105409-102105425
17	BHLHE40	chr7:102105028-102105670	K562	blood:	n/a	chr7:102105343-102105359 chr7:102105409-102105425
18	BRCA1	chr7:102105238-102105495	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:102107666-102107866	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:102107676-102107680	HepG2	liver:	n/a	n/a
21	BRCA1	chr7:102105131-102105589	HepG2	liver:	n/a	n/a
22	BRCA1	chr7:102105043-102105492	GM12878	blood:	n/a	n/a
23	CBX3	chr7:102104440-102105788	K562	blood:	n/a	n/a
24	CCNT2	chr7:102109140-102109266	K562	blood:	n/a	n/a
25	CCNT2	chr7:102105109-102105718	K562	blood:	n/a	n/a
26	CEBPB	chr7:102105268-102105644	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:102105250-102105458	GM12878	blood:	n/a	n/a
28	CEBPD	chr7:102105226-102105633	HepG2	liver:	n/a	n/a
29	CHD1	chr7:102105332-102105854	GM12878	blood:	n/a	n/a
30	CHD1	chr7:102105968-102105976	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:102105097-102105518	K562	blood:	n/a	n/a
32	CHD2	chr7:102104973-102105628	GM12878	blood:	n/a	n/a
33	CHD2	chr7:102105035-102105755	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr7:102105044-102105606	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr7:102104946-102105631	HepG2	liver:	n/a	n/a
36	CHD2	chr7:102107547-102107747	GM12878	blood:	n/a	n/a
37	CREB1	chr7:102105108-102105614	A549	lung:	n/a	n/a
38	CREB1	chr7:102105296-102105555	A549	lung:	n/a	n/a
39	CREB1	chr7:102104730-102105812	HepG2	liver:	n/a	n/a
40	CREB1	chr7:102105174-102105661	ECC-1	luminal epithelium:	n/a	n/a
41	CTCF	chr7:102107620-102107770	SAEC	small airway:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
42	CTCF	chr7:102105380-102105530	GM06990	blood:	n/a	chr7:102105413-102105426
43	CTCF	chr7:102105612-102105615	GM12878	blood:	n/a	n/a
44	CTCF	chr7:102107600-102107750	HMF	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
45	CTCF	chr7:102105340-102105534	GM10248	blood:	n/a	chr7:102105413-102105426
46	CTCF	chr7:102107620-102107770	SK-N-SH_RA	brain:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
47	CTCF	chr7:102107960-102108110	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr7:102105120-102105270	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr7:102107640-102107790	AoAF	blood vessel:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
50	CTCF	chr7:102107490-102107927	IMR90	lung:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102109446-102109496	ECC-1	luminal epithelium:	n/a
2	chr7:102104916-102104966	NB4	blood:	n/a
3	chr7:102105641-102105691	HL-60	blood:	n/a
4	chr7:102109446-102109496	ECC-1	luminal epithelium:	n/a
5	chr7:102104916-102104966	NB4	blood:	n/a
6	chr7:102105641-102105691	HL-60	blood:	n/a
7	chr7:102104807-102104857	Hepatocyte	liver:	n/a
8	chr7:102105753-102105803	HEK293	kidney:	embryo
9	chr7:102109247-102109297	K562	blood:	n/a
10	chr7:102107737-102107787	IMR90	lung:	fetal
11	chr7:102105344-102105394	Caco-2	colon:	n/a
12	chr7:102105195-102105245	SK-N-MC	brain:	n/a
13	chr7:102105205-102105255	Jurkat	blood:	n/a
14	chr7:102105195-102105245	HCM	heart:	n/a
15	chr7:102109247-102109297	HCF	heart:	n/a
16	chr7:102104807-102104857	ProgFib	skin:	n/a
17	chr7:102107737-102107787	ECC-1	luminal epithelium:	n/a
18	chr7:102105256-102105306	H1-hESC	embryonic stem cell:	embryo
19	chr7:102105205-102105255	HNPCEpiC	eye:	n/a
20	chr7:102105344-102105394	HCPEpiC	choroid plexus:	n/a
21	chr7:102109247-102109297	HCM	heart:	n/a
22	chr7:102105205-102105255	AG09309	skin:	n/a
23	chr7:102105256-102105306	NHDF-neo	bronchial:	n/a
24	chr7:102104807-102104857	HCM	heart:	n/a
25	chr7:102105195-102105245	SAEC	small airway:	n/a
26	chr7:102105344-102105394	HIPEpiC	eye:	n/a
27	chr7:102109446-102109496	HUVEC	blood vessel:	n/a
28	chr7:102105641-102105691	HUVEC	blood vessel:	n/a
29	chr7:102104916-102104966	RPTEC	kidney:	n/a
30	chr7:102105344-102105394	U87	brain:	n/a
31	chr7:102105753-102105803	T-47D	breast:	n/a
32	chr7:102104297-102104347	T-47D	breast:	n/a
33	chr7:102105124-102105174	BE2_C	brain:	n/a
34	chr7:102105641-102105691	Caco-2	colon:	n/a
35	chr7:102107737-102107787	GM12892	blood:	n/a
36	chr7:102107737-102107787	AG04449	skin:	fetal
37	chr7:102105256-102105306	AG09309	skin:	n/a
38	chr7:102105124-102105174	Hepatocyte	liver:	n/a
39	chr7:102105753-102105803	SK-N-SH_RA	brain:	n/a
40	chr7:102105205-102105255	NH-A	brain:	n/a
41	chr7:102107737-102107787	AG09319	gingival:	n/a
42	chr7:102109247-102109297	AG04450	lung:	fetal
43	chr7:102109446-102109496	AG04449	skin:	fetal
44	chr7:102109247-102109297	GM12891	blood:	n/a
45	chr7:102105201-102105251	K562	blood:	n/a
46	chr7:102105205-102105255	LNCaP	prostate:	n/a
47	chr7:102109446-102109496	SK-N-SH_RA	brain:	n/a
48	chr7:102105781-102105831	AG04450	lung:	fetal
49	chr7:102105205-102105255	HRCEpiC	kidney:	n/a
50	chr7:102105781-102105831	HCF	heart:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:82462024..82463020-chr7:102105257..102105953,2	NB4	blood:
2	chr7:102073875..102075484-chr7:102103725..102106348,2	MCF-7	breast:
3	chr7:102092377..102094022-chr7:102102863..102104706,2	K562	blood:
4	chr7:102035604..102038403-chr7:102105375..102107150,2	K562	blood:
5	chr16:90039038..90039558-chr7:102105289..102105810,2	Hela-S3	cervix:
6	chr7:102085730..102086410-chr7:102110585..102111557,2	K562	blood:
7	chr7:102074336..102076927-chr7:102105688..102108273,2	K562	blood:
8	chr7:101929851..101931493-chr7:102106221..102107741,2	MCF-7	breast:
9	chr7:102110628..102112535-chr8:144951000..144953117,2	MCF-7	breast:
10	chr7:102110592..102113197-chr7:102117853..102119354,2	MCF-7	breast:
11	chr10:12391000..12393664-chr7:102102754..102105293,2	MCF-7	breast:
12	chr7:101935058..101937626-chr7:102103527..102105838,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5090	chr7:102106199-102106221	MIMAT0021082

No data

Variant related genes	Relation type
MIR5090	TF binding region
MIR4467	TF binding region
LRWD1	TF binding region
ALKBH4	TF binding region
MIR5090	CpG island
MIR4467	CpG island
LRWD1	CpG island
ALKBH4	CpG island
ENSG00000264675	chromatin interactions
ENSG00000183049	chromatin interactions
ENSG00000160991	chromatin interactions
ENSG00000112773	chromatin interactions
ENSG00000239480	chromatin interactions
ENSG00000227184	chromatin interactions
ENSG00000128563	chromatin interactions
ENSG00000223959	chromatin interactions
ENSG00000005075	chromatin interactions

Extended variants
information (count: 419 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6465866	chr7:102103293-102103294	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs56208004	chr7:102103294-102103295	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs528868745	chr7:102103372-102103373	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs543759108	chr7:102103382-102103383	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs190744817	chr7:102103386-102103387	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370280641	chr7:102103403-102103404	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs78507302	chr7:102103415-102103416	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs79075886	chr7:102103421-102103422	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs75836400	chr7:102103423-102103424	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527258028	chr7:102103514-102103515	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182024783	chr7:102103610-102103611	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs548992938	chr7:102103673-102103674	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs567302374	chr7:102103682-102103683	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs560316435	chr7:102103691-102103692	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs186314398	chr7:102103694-102103695	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs77384286	chr7:102103731-102103732	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs11487069	chr7:102103732-102103733	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs549445235	chr7:102103770-102103771	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs77928869	chr7:102103795-102103796	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs10234138	chr7:102103797-102103798	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs375202572	chr7:102103879-102103880	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs546893613	chr7:102103902-102103903	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs188363666	chr7:102103931-102103932	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs10234347	chr7:102103949-102103950	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs180673529	chr7:102103974-102103975	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs10234267	chr7:102104056-102104057	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs369652254	chr7:102104057-102104058	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs540166233	chr7:102104073-102104074	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs140637840	chr7:102104099-102104100	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs4403344	chr7:102104108-102104109	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs76191781	chr7:102104109-102104110	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs111294683	chr7:102104135-102104136	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs185747497	chr7:102104220-102104221	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs557919211	chr7:102104233-102104234	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs543888265	chr7:102104280-102104281	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs144404115	chr7:102104298-102104299	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs28538953	chr7:102104299-102104300	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191152226	chr7:102104363-102104364	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs560144986	chr7:102104468-102104469	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs67493080	chr7:102104486-102104487	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs527482765	chr7:102104490-102104491	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs548949559	chr7:102104491-102104492	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs537183877	chr7:102104492-102104493	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs555321289	chr7:102104493-102104494	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs78865278	chr7:102104494-102104495	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs398005637	chr7:102104495-102104496	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs561051486	chr7:102104498-102104499	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs529444661	chr7:102104621-102104622	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs75327203	chr7:102104634-102104635	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs183857380	chr7:102104672-102104673	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:952 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102075000-102104000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:102075200-102104200	Weak transcription	Fetal Kidney	kidney
3	chr7:102075600-102103400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr7:102075800-102103600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr7:102076000-102104200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr7:102081200-102104200	Weak transcription	Right Atrium	heart
7	chr7:102084400-102104000	Weak transcription	Fetal Brain Male	brain
8	chr7:102088200-102104200	Weak transcription	HUVEC	blood vessel
9	chr7:102088400-102104000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:102092400-102104200	Weak transcription	Psoas Muscle	Psoas
11	chr7:102092400-102104200	Weak transcription	Stomach Mucosa	stomach
12	chr7:102092400-102104200	Weak transcription	A549	lung
13	chr7:102092400-102104200	Weak transcription	HSMM	muscle
14	chr7:102092400-102104200	Weak transcription	NHDF-Ad	bronchial
15	chr7:102092600-102104000	Weak transcription	HSMMtube	muscle
16	chr7:102092600-102104200	Weak transcription	HMEC	breast
17	chr7:102092600-102104200	Weak transcription	NHEK	skin
18	chr7:102094800-102103400	Strong transcription	Fetal Stomach	stomach
19	chr7:102095200-102103400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr7:102097800-102104000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr7:102097800-102104200	Weak transcription	NH-A	brain
22	chr7:102098400-102104000	Weak transcription	GM12878-XiMat	blood
23	chr7:102098600-102104200	Weak transcription	Hela-S3	cervix
24	chr7:102098800-102104000	Weak transcription	Colon Smooth Muscle	Colon
25	chr7:102098800-102104200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr7:102098800-102104200	Weak transcription	Colonic Mucosa	Colon
27	chr7:102098800-102104200	Weak transcription	K562	blood
28	chr7:102098800-102104400	Weak transcription	Small Intestine	intestine
29	chr7:102099000-102104000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:102099000-102104200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr7:102099000-102104200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr7:102099000-102104200	Weak transcription	Primary B cells from cord blood	blood
33	chr7:102099000-102104200	Weak transcription	NHLF	lung
34	chr7:102099200-102104000	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr7:102099200-102104000	Weak transcription	HepG2	liver
36	chr7:102099400-102104200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr7:102099600-102104200	Weak transcription	Osteobl	bone
38	chr7:102100000-102104000	Weak transcription	Primary B cells from peripheral blood	blood
39	chr7:102100000-102104000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr7:102100000-102104000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr7:102100000-102104000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr7:102100000-102104000	Weak transcription	Pancreas	Pancrea
43	chr7:102100000-102104200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr7:102100000-102104200	Weak transcription	Brain Angular Gyrus	brain
45	chr7:102100000-102104200	Weak transcription	Brain Substantia Nigra	brain
46	chr7:102100000-102104200	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr7:102100200-102103800	Weak transcription	Left Ventricle	heart
48	chr7:102100200-102104000	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr7:102100200-102104000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr7:102100200-102104000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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