Variant report

Variant	nsv889078
Chromosome Location	chr7:117135025-117246315
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:122)
Chromatin interactive
region (count:34)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:117195388-117195586	K562	blood:	n/a	n/a
2	ATF2	chr7:117228256-117228885	GM12878	blood:	n/a	n/a
3	ATF2	chr7:117228213-117228911	GM12878	blood:	n/a	n/a
4	ATF3	chr7:117228178-117228937	A549	lung:	n/a	n/a
5	ATF3	chr7:117222102-117222912	A549	lung:	n/a	n/a
6	ATF3	chr7:117222180-117222830	A549	lung:	n/a	n/a
7	BACH1	chr7:117188133-117188349	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:117245114-117245164	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr7:117204164-117204384	GM12878	blood:	n/a	n/a
10	BATF	chr7:117228364-117228827	GM12878	blood:	n/a	chr7:117228615-117228626
11	BCL11A	chr7:117228325-117228839	GM12878	blood:	n/a	n/a
12	BCL3	chr7:117245619-117246225	A549	lung:	n/a	n/a
13	BCL3	chr7:117228101-117228945	A549	lung:	n/a	n/a
14	BCL3	chr7:117222144-117222940	A549	lung:	n/a	chr7:117222627-117222634
15	BCL3	chr7:117222062-117223040	A549	lung:	n/a	chr7:117222627-117222634
16	BCL3	chr7:117228214-117228853	A549	lung:	n/a	n/a
17	BCLAF1	chr7:117228370-117228794	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:117243779-117244031	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:117204094-117204536	GM12878	blood:	n/a	chr7:117204311-117204320 chr7:117204311-117204320
20	BHLHE40	chr7:117228373-117228856	GM12878	blood:	n/a	n/a
21	BRCA1	chr7:117245834-117246047	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr7:117222167-117222831	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr7:117228113-117228980	Hela-S3	cervix:	n/a	chr7:117228650-117228657
24	CEBPB	chr7:117171738-117171964	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:117222032-117222940	Hela-S3	cervix:	n/a	chr7:117222302-117222313
26	CEBPB	chr7:117202940-117203217	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:117143403-117143622	HepG2	liver:	n/a	chr7:117143483-117143494 chr7:117143481-117143494 chr7:117143481-117143492
28	CEBPB	chr7:117245562-117246203	A549	lung:	n/a	n/a
29	CEBPB	chr7:117228349-117228788	MCF-7	breast:	n/a	chr7:117228586-117228597
30	CEBPB	chr7:117222244-117222431	K562	blood:	n/a	chr7:117222302-117222313
31	CEBPB	chr7:117206581-117206695	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr7:117143495-117143528	K562	blood:	n/a	n/a
33	CEBPB	chr7:117245738-117246078	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:117213004-117213146	A549	lung:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
35	CEBPB	chr7:117212837-117213239	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
36	CEBPB	chr7:117228431-117228821	IMR90	lung:	n/a	chr7:117228586-117228597
37	CEBPB	chr7:117170361-117170547	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:117228203-117228832	A549	lung:	n/a	chr7:117228586-117228597
39	CEBPB	chr7:117212851-117213351	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
40	CEBPB	chr7:117202921-117203156	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:117161167-117161444	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:117171679-117171984	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:117221920-117222859	A549	lung:	n/a	chr7:117222302-117222313
44	CEBPB	chr7:117222133-117222567	HepG2	liver:	n/a	chr7:117222302-117222313
45	CEBPB	chr7:117143393-117143626	IMR90	lung:	n/a	chr7:117143483-117143494 chr7:117143481-117143494 chr7:117143481-117143492
46	CEBPB	chr7:117191755-117191958	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:117221884-117223012	A549	lung:	n/a	chr7:117222302-117222313
48	CEBPB	chr7:117227809-117228967	Hela-S3	cervix:	n/a	chr7:117228586-117228597
49	CEBPB	chr7:117222054-117222935	A549	lung:	n/a	chr7:117222302-117222313
50	CEBPB	chr7:117198075-117198115	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:117171038-117171088	HCM	heart:	n/a
2	chr7:117171038-117171088	NHDF-neo	bronchial:	n/a
3	chr7:117228958-117229008	ProgFib	skin:	n/a
4	chr7:117171038-117171088	LNCaP	prostate:	n/a
5	chr7:117228958-117229008	CMK	blood:	n/a
6	chr7:117171038-117171088	HRCEpiC	kidney:	n/a
7	chr7:117228958-117229008	LNCaP	prostate:	n/a
8	chr7:117228958-117229008	BJ	skin:	n/a
9	chr7:117228958-117229008	HepG2	liver:	n/a
10	chr7:117171038-117171088	SKMC	muscle:	n/a
11	chr7:117228958-117229008	HCF	heart:	n/a
12	chr7:117228958-117229008	Caco-2	colon:	n/a
13	chr7:117171038-117171088	Jurkat	blood:	n/a
14	chr7:117228958-117229008	GM19239	blood:	n/a
15	chr7:117171038-117171088	NT2-D1	testis:	n/a
16	chr7:117228958-117229008	HRCEpiC	kidney:	n/a
17	chr7:117171038-117171088	AG04449	skin:	fetal
18	chr7:117171038-117171088	HepG2	liver:	n/a
19	chr7:117228958-117229008	HRPEpiC	eye:	n/a
20	chr7:117171038-117171088	HEK293	kidney:	embryo
21	chr7:117228958-117229008	AG09319	gingival:	n/a
22	chr7:117171038-117171088	HNPCEpiC	eye:	n/a
23	chr7:117171038-117171088	RPTEC	kidney:	n/a
24	chr7:117228958-117229008	NHDF-neo	bronchial:	n/a
25	chr7:117228958-117229008	Jurkat	blood:	n/a
26	chr7:117228958-117229008	U87	brain:	n/a
27	chr7:117228958-117229008	NHBE	bronchial:	n/a
28	chr7:117228958-117229008	NH-A	brain:	n/a
29	chr7:117228958-117229008	T-47D	breast:	n/a
30	chr7:117171038-117171088	AG10803	skin:	n/a
31	chr7:117171038-117171088	ProgFib	skin:	n/a
32	chr7:117171038-117171088	GM12892	blood:	n/a
33	chr7:117228958-117229008	NT2-D1	testis:	n/a
34	chr7:117171038-117171088	HEEpiC	esophagus:	n/a
35	chr7:117171038-117171088	HAEpiC	amniotic membrane:	n/a
36	chr7:117171038-117171088	IMR90	lung:	fetal
37	chr7:117171038-117171088	BE2_C	brain:	n/a
38	chr7:117228958-117229008	MCF10A-Er-Src	breast:	n/a
39	chr7:117171038-117171088	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:117228958-117229008	HEEpiC	esophagus:	n/a
41	chr7:117171038-117171088	ovcar-3	ovarian:	n/a
42	chr7:117228958-117229008	NB4	blood:	n/a
43	chr7:117228958-117229008	MCF-7	breast:	n/a
44	chr7:117228958-117229008	SK-N-SH	brain:	n/a
45	chr7:117171038-117171088	A549	lung:	n/a
46	chr7:117228958-117229008	K562	blood:	n/a
47	chr7:117171038-117171088	GM06990	blood:	n/a
48	chr7:117228958-117229008	SKMC	muscle:	n/a
49	chr7:117228958-117229008	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:117171038-117171088	SK-N-MC	brain:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
2	chr12:58237960..58239522-chr7:117246298..117249075,2	MCF-7	breast:
3	7:116754962-116765597..7:117228556-117233275	Hela-S3	cervix:
4	7:115890993-115892266..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
5	chr7:117244166..117245859-chr7:117250473..117252926,2	MCF-7	breast:
6	chr7:117171466..117173089-chr7:117174919..117176705,2	K562	blood:
7	7:116544149-116547624..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
8	chr7:117142868..117145143-chr7:117146989..117148912,2	K562	blood:
9	7:115847372-115857098..7:117167208-117172399	H1-hESC	embryonic stem cell:	embryo
10	chr7:115543985..115545868-chr7:117149262..117151198,2	MCF-7	breast:
11	7:115847372-115857098..7:117228556-117233275	H1-hESC	embryonic stem cell:	embryo
12	7:115847372-115857098..7:117179549-117182665	H1-hESC	embryonic stem cell:	embryo
13	chr7:117173270..117176194-chr7:117177984..117179733,2	MCF-7	breast:
14	chr7:117180519..117183145-chr7:117187916..117190717,2	K562	blood:
15	7:115861595-115870968..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
16	chr7:117184115..117186355-chr7:117188163..117190019,2	K562	blood:
17	7:116604327-116608063..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
18	7:115847372-115857098..7:117194433-117196955	H1-hESC	embryonic stem cell:	embryo
19	7:117100350-117112126..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
20	7:117065049-117068137..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
21	chr7:117180519..117183145-chr7:117187916..117190717,2	K562	blood:
22	chr7:117171466..117173089-chr7:117174919..117176705,2	K562	blood:
23	7:117100350-117112126..7:117167208-117172399	H1-hESC	embryonic stem cell:	embryo
24	chr3:27573830..27575693-chr7:117148842..117151138,2	MCF-7	breast:
25	chr7:117173270..117176194-chr7:117177984..117179733,2	MCF-7	breast:
26	chr7:117142868..117145143-chr7:117146989..117148912,2	K562	blood:
27	7:115861595-115870968..7:117216968-117220729	H1-hESC	embryonic stem cell:	embryo
28	7:117100350-117112126..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
29	chr7:117184115..117186355-chr7:117188163..117190019,2	K562	blood:
30	chr7:117190103..117191769-chr7:117198785..117201652,2	K562	blood:
31	7:116957165-116964911..7:117151441-117153264	H1-hESC	embryonic stem cell:	embryo
32	chr7:117203452..117206266-chr7:117206487..117208495,3	MCF-7	breast:
33	7:115847372-115857098..7:117137230-117139328	Hela-S3	cervix:
34	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASZ1-1	chr7:117204570-117204730	ENSG00000232661.1
2	lnc-CFTR-2	chr7:117144308-117144362	NONHSAT122944
3	lnc-CTTNBP2-4	chr7:117226261-117226470	NONHSAT122949
4	lnc-CTTNBP2-1	chr7:117244845-117245043	ENSG00000083622.8
5	lnc-ASZ1-1	chr7:117200787-117200846	ENSG00000232661.1

No data

Variant related genes	Relation type
CFTR	TF binding region
ENSG00000234001	TF binding region
ENSG00000232661	TF binding region
CFTR	CpG island
ENSG00000234001	CpG island
ENSG00000232661	CpG island
ENSG00000228368	chromatin interactions
ENSG00000232661	chromatin interactions
ENSG00000004866	chromatin interactions
ENSG00000175215	chromatin interactions
ENSG00000001626	chromatin interactions
ENSG00000105989	chromatin interactions
ENSG00000154438	chromatin interactions
ENSG00000135269	chromatin interactions

Extended variants
information (count: 4186 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4186 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4148688	chr7:117135025-117135026	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574747569	chr7:117135099-117135100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535481849	chr7:117135106-117135107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554098747	chr7:117135125-117135126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572479439	chr7:117135153-117135154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17545644	chr7:117135212-117135213	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557713052	chr7:117135236-117135237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552878712	chr7:117135249-117135250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192561615	chr7:117135293-117135294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35313680	chr7:117135392-117135393	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs113527763	chr7:117135413-117135414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112371844	chr7:117135438-117135439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561966045	chr7:117135440-117135441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184931344	chr7:117135475-117135476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142997603	chr7:117135478-117135479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146152437	chr7:117135507-117135508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77491337	chr7:117135512-117135513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575386042	chr7:117135521-117135522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189460519	chr7:117135525-117135526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181734690	chr7:117135537-117135538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140196396	chr7:117135583-117135584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549937495	chr7:117135608-117135609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568426336	chr7:117135633-117135634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535348607	chr7:117135644-117135645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563531507	chr7:117135701-117135702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548882363	chr7:117135715-117135716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553904869	chr7:117135724-117135725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373192216	chr7:117135768-117135769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566060224	chr7:117135784-117135785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34360978	chr7:117135833-117135834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539586997	chr7:117135989-117135990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117629380	chr7:117136019-117136020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576557842	chr7:117136050-117136051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534535991	chr7:117136057-117136058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73484603	chr7:117136059-117136060	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs184482103	chr7:117136074-117136075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34792223	chr7:117136083-117136084	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs541316536	chr7:117136108-117136109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559127433	chr7:117136129-117136130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34427586	chr7:117136143-117136144	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs559817768	chr7:117136210-117136211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148934096	chr7:117136211-117136212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148422231	chr7:117136242-117136243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6944750	chr7:117136252-117136253	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs530491492	chr7:117136260-117136261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189967427	chr7:117136266-117136267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577755963	chr7:117136269-117136270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181360386	chr7:117136283-117136284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186327948	chr7:117136355-117136356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548059041	chr7:117136357-117136358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Squamous cell cancer	20885788	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Glioblastoma multiforme	21922591	CNVD
Sudden cardiac death	19188705	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117126800-117151200	Weak transcription	Pancreas	Pancrea
2	chr7:117129800-117144600	Weak transcription	Duodenum Mucosa	Duodenum
3	chr7:117131200-117139600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr7:117134200-117135200	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr7:117134400-117136200	Enhancers	Fetal Intestine Small	intestine
6	chr7:117134600-117136400	Enhancers	Fetal Intestine Large	intestine
7	chr7:117135200-117135800	Enhancers	Small Intestine	intestine
8	chr7:117135200-117142200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr7:117135800-117141200	Weak transcription	Small Intestine	intestine
10	chr7:117136200-117139400	Weak transcription	Fetal Intestine Small	intestine
11	chr7:117136400-117141000	Weak transcription	Fetal Intestine Large	intestine
12	chr7:117139400-117140200	Enhancers	Fetal Intestine Small	intestine
13	chr7:117139600-117140000	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr7:117139600-117140200	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr7:117140000-117142000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr7:117140200-117142000	Weak transcription	Fetal Intestine Small	intestine
17	chr7:117140200-117142000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:117141000-117142800	Enhancers	Fetal Intestine Large	intestine
19	chr7:117141200-117141400	Enhancers	Small Intestine	intestine
20	chr7:117141400-117141800	Weak transcription	Small Intestine	intestine
21	chr7:117141800-117143200	Enhancers	Small Intestine	intestine
22	chr7:117142000-117143200	Enhancers	Fetal Intestine Small	intestine
23	chr7:117142000-117143200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr7:117142000-117143200	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr7:117142200-117142400	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr7:117142400-117147000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:117142800-117145200	Weak transcription	Fetal Intestine Large	intestine
28	chr7:117143200-117145600	Weak transcription	Fetal Intestine Small	intestine
29	chr7:117143200-117147000	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr7:117143200-117152600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr7:117144600-117145800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:117144600-117147800	Strong transcription	Duodenum Mucosa	Duodenum
33	chr7:117144800-117145400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:117145200-117146400	Strong transcription	Fetal Intestine Large	intestine
35	chr7:117145600-117146600	Strong transcription	Fetal Intestine Small	intestine
36	chr7:117146400-117151000	Weak transcription	Fetal Intestine Large	intestine
37	chr7:117146600-117151200	Weak transcription	Fetal Intestine Small	intestine
38	chr7:117146800-117147200	Enhancers	Liver	Liver
39	chr7:117147000-117147800	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr7:117147000-117147800	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr7:117147800-117148800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr7:117147800-117150400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr7:117147800-117151000	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr7:117148800-117149000	Genic enhancers	Rectal Mucosa Donor 31	rectum
45	chr7:117149000-117149200	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr7:117149200-117151200	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr7:117150400-117153800	Strong transcription	Duodenum Mucosa	Duodenum
48	chr7:117151000-117154400	Strong transcription	Fetal Intestine Large	intestine
49	chr7:117151000-117154400	Strong transcription	Rectal Mucosa Donor 29	rectum
50	chr7:117151200-117151800	Strong transcription	Fetal Intestine Small	intestine

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