Variant report

Variant	nsv889077
Chromosome Location	chr7:117129404-117238379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:546)
CpG islands
(count:122)
Chromatin interactive
region (count:30)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:546 , 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	ARID3A	chr7:117130015-117130462	HepG2	liver:	n/a	n/a
2	ATF1	chr7:117195388-117195586	K562	blood:	n/a	n/a
3	ATF2	chr7:117228213-117228911	GM12878	blood:	n/a	n/a
4	ATF2	chr7:117228256-117228885	GM12878	blood:	n/a	n/a
5	ATF3	chr7:117228178-117228937	A549	lung:	n/a	n/a
6	ATF3	chr7:117222180-117222830	A549	lung:	n/a	n/a
7	ATF3	chr7:117222102-117222912	A549	lung:	n/a	n/a
8	BACH1	chr7:117188133-117188349	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr7:117228364-117228827	GM12878	blood:	n/a	chr7:117228615-117228626
10	BATF	chr7:117204164-117204384	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:117228325-117228839	GM12878	blood:	n/a	n/a
12	BCL3	chr7:117228214-117228853	A549	lung:	n/a	n/a
13	BCL3	chr7:117222144-117222940	A549	lung:	n/a	chr7:117222627-117222634
14	BCL3	chr7:117228101-117228945	A549	lung:	n/a	n/a
15	BCL3	chr7:117222062-117223040	A549	lung:	n/a	chr7:117222627-117222634
16	BCLAF1	chr7:117228370-117228794	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:117228373-117228856	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:117204094-117204536	GM12878	blood:	n/a	chr7:117204311-117204320 chr7:117204311-117204320
19	BRCA1	chr7:117228113-117228980	Hela-S3	cervix:	n/a	chr7:117228650-117228657
20	BRCA1	chr7:117222167-117222831	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:117171738-117171964	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:117143393-117143626	IMR90	lung:	n/a	chr7:117143483-117143494 chr7:117143481-117143494 chr7:117143481-117143492
23	CEBPB	chr7:117227809-117228967	Hela-S3	cervix:	n/a	chr7:117228586-117228597
24	CEBPB	chr7:117206581-117206695	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:117170361-117170547	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:117228036-117228960	A549	lung:	n/a	chr7:117228586-117228597
27	CEBPB	chr7:117228349-117228788	MCF-7	breast:	n/a	chr7:117228586-117228597
28	CEBPB	chr7:117213004-117213146	A549	lung:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
29	CEBPB	chr7:117212837-117213239	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
30	CEBPB	chr7:117161167-117161444	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:117200161-117200427	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:117129984-117130381	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:117228431-117228821	IMR90	lung:	n/a	chr7:117228586-117228597
34	CEBPB	chr7:117202940-117203217	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:117212851-117213351	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
36	CEBPB	chr7:117222133-117222567	HepG2	liver:	n/a	chr7:117222302-117222313
37	CEBPB	chr7:117222032-117222940	Hela-S3	cervix:	n/a	chr7:117222302-117222313
38	CEBPB	chr7:117221920-117222859	A549	lung:	n/a	chr7:117222302-117222313
39	CEBPB	chr7:117222135-117222657	MCF-7	breast:	n/a	chr7:117222302-117222313
40	CEBPB	chr7:117134899-117135147	A549	lung:	n/a	n/a
41	CEBPB	chr7:117221884-117223012	A549	lung:	n/a	chr7:117222302-117222313
42	CEBPB	chr7:117129976-117130460	A549	lung:	n/a	n/a
43	CEBPB	chr7:117191755-117191958	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:117171672-117172026	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr7:117222117-117222867	IMR90	lung:	n/a	chr7:117222302-117222313
46	CEBPB	chr7:117228203-117228832	A549	lung:	n/a	chr7:117228586-117228597
47	CEBPB	chr7:117202921-117203156	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:117171679-117171984	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:117200159-117200394	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:117202887-117203267	Hela-S3	cervix:	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	SK-N-SH	brain:	n/a
2	chr7:117228958-117229008	SK-N-MC	brain:	n/a
3	chr7:117171038-117171088	Hepatocyte	liver:	n/a
4	chr7:117228958-117229008	ProgFib	skin:	n/a
5	chr7:117228958-117229008	AoSMC	blood vessel:	n/a
6	chr7:117228958-117229008	BE2_C	brain:	n/a
7	chr7:117171038-117171088	BE2_C	brain:	n/a
8	chr7:117228958-117229008	ECC-1	luminal epithelium:	n/a
9	chr7:117171038-117171088	HCF	heart:	n/a
10	chr7:117228958-117229008	PANC-1	pancreas:	n/a
11	chr7:117228958-117229008	GM12891	blood:	n/a
12	chr7:117171038-117171088	HEEpiC	esophagus:	n/a
13	chr7:117171038-117171088	HL-60	blood:	n/a
14	chr7:117171038-117171088	HUVEC	blood vessel:	n/a
15	chr7:117171038-117171088	NHDF-neo	bronchial:	n/a
16	chr7:117171038-117171088	ECC-1	luminal epithelium:	n/a
17	chr7:117171038-117171088	GM12878	blood:	n/a
18	chr7:117228958-117229008	U87	brain:	n/a
19	chr7:117228958-117229008	Hepatocyte	liver:	n/a
20	chr7:117228958-117229008	NB4	blood:	n/a
21	chr7:117228958-117229008	GM19239	blood:	n/a
22	chr7:117228958-117229008	ovcar-3	ovarian:	n/a
23	chr7:117228958-117229008	AG09319	gingival:	n/a
24	chr7:117228958-117229008	BJ	skin:	n/a
25	chr7:117228958-117229008	RPTEC	kidney:	n/a
26	chr7:117228958-117229008	GM12892	blood:	n/a
27	chr7:117171038-117171088	HCM	heart:	n/a
28	chr7:117228958-117229008	HMEC	breast:	n/a
29	chr7:117228958-117229008	Jurkat	blood:	n/a
30	chr7:117171038-117171088	GM19239	blood:	n/a
31	chr7:117228958-117229008	NH-A	brain:	n/a
32	chr7:117228958-117229008	HAEpiC	amniotic membrane:	n/a
33	chr7:117228958-117229008	PrEC	prostate:	n/a
34	chr7:117228958-117229008	HRE	kidney:	n/a
35	chr7:117228958-117229008	SK-N-SH	brain:	n/a
36	chr7:117228958-117229008	NHDF-neo	bronchial:	n/a
37	chr7:117171038-117171088	A549	lung:	n/a
38	chr7:117171038-117171088	ProgFib	skin:	n/a
39	chr7:117171038-117171088	MCF10A-Er-Src	breast:	n/a
40	chr7:117228958-117229008	HCF	heart:	n/a
41	chr7:117171038-117171088	Jurkat	blood:	n/a
42	chr7:117228958-117229008	GM12878	blood:	n/a
43	chr7:117171038-117171088	RPTEC	kidney:	n/a
44	chr7:117171038-117171088	HRCEpiC	kidney:	n/a
45	chr7:117171038-117171088	AG04449	skin:	fetal
46	chr7:117171038-117171088	NT2-D1	testis:	n/a
47	chr7:117171038-117171088	SKMC	muscle:	n/a
48	chr7:117171038-117171088	PFSK-1	brain:	n/a
49	chr7:117171038-117171088	AoSMC	blood vessel:	n/a
50	chr7:117228958-117229008	HEK293	kidney:	embryo

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:117100350-117112126..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
2	chr7:117125349..117127629-chr7:117128449..117131310,2	MCF-7	breast:
3	chr7:117184115..117186355-chr7:117188163..117190019,2	K562	blood:
4	7:117065049-117068137..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
5	7:115847372-115857098..7:117194433-117196955	H1-hESC	embryonic stem cell:	embryo
6	7:115861595-115870968..7:117216968-117220729	H1-hESC	embryonic stem cell:	embryo
7	chr7:117142868..117145143-chr7:117146989..117148912,2	K562	blood:
8	7:116957165-116964911..7:117151441-117153264	H1-hESC	embryonic stem cell:	embryo
9	7:117100350-117112126..7:117167208-117172399	H1-hESC	embryonic stem cell:	embryo
10	chr7:117142868..117145143-chr7:117146989..117148912,2	K562	blood:
11	chr7:117180519..117183145-chr7:117187916..117190717,2	K562	blood:
12	chr7:117190103..117191769-chr7:117198785..117201652,2	K562	blood:
13	chr7:115543985..115545868-chr7:117149262..117151198,2	MCF-7	breast:
14	7:115847372-115857098..7:117179549-117182665	H1-hESC	embryonic stem cell:	embryo
15	chr7:117180519..117183145-chr7:117187916..117190717,2	K562	blood:
16	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
17	chr7:117203452..117206266-chr7:117206487..117208495,3	MCF-7	breast:
18	chr7:117184115..117186355-chr7:117188163..117190019,2	K562	blood:
19	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
20	7:116754962-116765597..7:117228556-117233275	Hela-S3	cervix:
21	7:115847372-115857098..7:117228556-117233275	H1-hESC	embryonic stem cell:	embryo
22	chr7:117171466..117173089-chr7:117174919..117176705,2	K562	blood:
23	7:115890993-115892266..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
24	chr7:117173270..117176194-chr7:117177984..117179733,2	MCF-7	breast:
25	chr7:117171466..117173089-chr7:117174919..117176705,2	K562	blood:
26	7:115847372-115857098..7:117167208-117172399	H1-hESC	embryonic stem cell:	embryo
27	7:115847372-115857098..7:117137230-117139328	Hela-S3	cervix:
28	chr7:117173270..117176194-chr7:117177984..117179733,2	MCF-7	breast:
29	chr3:27573830..27575693-chr7:117148842..117151138,2	MCF-7	breast:
30	7:116604327-116608063..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo

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

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

No data

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

Extended variants
information (count: 4065 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4065 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs885993	chr7:117129404-117129405	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576167686	chr7:117129439-117129440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530186612	chr7:117129469-117129470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs17139943	chr7:117129491-117129492	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs372877302	chr7:117129500-117129501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77341775	chr7:117129559-117129560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533483613	chr7:117129560-117129561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139742880	chr7:117129562-117129563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34092224	chr7:117129575-117129576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570213946	chr7:117129643-117129644	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192793798	chr7:117129787-117129788	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555771288	chr7:117129814-117129815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567778356	chr7:117129820-117129821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535107915	chr7:117129827-117129828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553234674	chr7:117129870-117129871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577767189	chr7:117129953-117129954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555822628	chr7:117129988-117129989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545013503	chr7:117129989-117129990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534000900	chr7:117129995-117129996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535433911	chr7:117130007-117130008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144509507	chr7:117130044-117130045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572253410	chr7:117130054-117130055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542236405	chr7:117130055-117130056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35714998	chr7:117130142-117130143	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs75832262	chr7:117130145-117130146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184256167	chr7:117130225-117130226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559737230	chr7:117130284-117130285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373536993	chr7:117130297-117130298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533582516	chr7:117130313-117130314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551637682	chr7:117130320-117130321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370571182	chr7:117130366-117130367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150213129	chr7:117130367-117130368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564849701	chr7:117130404-117130405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs3034759	chr7:117130409-117130410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541835989	chr7:117130482-117130483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373679190	chr7:117130503-117130504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146293137	chr7:117130528-117130529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190744864	chr7:117130532-117130533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531197946	chr7:117130544-117130545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75791292	chr7:117130545-117130546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182210324	chr7:117130556-117130557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186324105	chr7:117130580-117130581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1557630	chr7:117130643-117130644	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs571607124	chr7:117130676-117130677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538828827	chr7:117130681-117130682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571231302	chr7:117130744-117130745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77540407	chr7:117130755-117130756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139808242	chr7:117130766-117130767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142086587	chr7:117130795-117130796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563854862	chr7:117130814-117130815	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:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117124000-117132200	Enhancers	Fetal Intestine Small	intestine
2	chr7:117126800-117151200	Weak transcription	Pancreas	Pancrea
3	chr7:117127400-117132400	Weak transcription	Dnd41	blood
4	chr7:117128400-117131000	Enhancers	Fetal Intestine Large	intestine
5	chr7:117128800-117129600	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr7:117128800-117131200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr7:117129000-117129600	Enhancers	Duodenum Mucosa	Duodenum
8	chr7:117129200-117130800	Enhancers	A549	lung
9	chr7:117129400-117130800	Enhancers	Liver	Liver
10	chr7:117129600-117129800	Flanking Active TSS	Duodenum Mucosa	Duodenum
11	chr7:117129600-117129800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
12	chr7:117129600-117129800	Enhancers	Small Intestine	intestine
13	chr7:117129600-117130600	Enhancers	HepG2	liver
14	chr7:117129600-117130800	Enhancers	Stomach Mucosa	stomach
15	chr7:117129800-117130200	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr7:117129800-117144600	Weak transcription	Duodenum Mucosa	Duodenum
17	chr7:117130200-117130600	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr7:117130600-117130800	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr7:117130800-117132400	Weak transcription	Liver	Liver
20	chr7:117130800-117134200	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr7:117131000-117134600	Weak transcription	Fetal Intestine Large	intestine
22	chr7:117131200-117139600	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr7:117132200-117132600	Weak transcription	Fetal Intestine Small	intestine
24	chr7:117132400-117133600	Enhancers	Liver	Liver
25	chr7:117132400-117134000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr7:117132400-117134200	Enhancers	Dnd41	blood
27	chr7:117132600-117132800	Enhancers	Fetal Intestine Small	intestine
28	chr7:117132800-117133200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:117132800-117133800	Weak transcription	Fetal Intestine Small	intestine
30	chr7:117133800-117134000	Enhancers	Fetal Intestine Small	intestine
31	chr7:117133800-117134000	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr7:117134000-117134400	Weak transcription	Fetal Intestine Small	intestine
33	chr7:117134200-117135200	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr7:117134400-117136200	Enhancers	Fetal Intestine Small	intestine
35	chr7:117134600-117136400	Enhancers	Fetal Intestine Large	intestine
36	chr7:117135200-117135800	Enhancers	Small Intestine	intestine
37	chr7:117135200-117142200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr7:117135800-117141200	Weak transcription	Small Intestine	intestine
39	chr7:117136200-117139400	Weak transcription	Fetal Intestine Small	intestine
40	chr7:117136400-117141000	Weak transcription	Fetal Intestine Large	intestine
41	chr7:117139400-117140200	Enhancers	Fetal Intestine Small	intestine
42	chr7:117139600-117140000	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr7:117139600-117140200	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr7:117140000-117142000	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr7:117140200-117142000	Weak transcription	Fetal Intestine Small	intestine
46	chr7:117140200-117142000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr7:117141000-117142800	Enhancers	Fetal Intestine Large	intestine
48	chr7:117141200-117141400	Enhancers	Small Intestine	intestine
49	chr7:117141400-117141800	Weak transcription	Small Intestine	intestine
50	chr7:117141800-117143200	Enhancers	Small Intestine	intestine

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