Variant report

Variant	nsv1031750
Chromosome Location	chr7:103031836-103067306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:103031745-103031971	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:103047367-103047695	HepG2	liver:	n/a	n/a
3	ATF3	chr7:103063956-103064212	K562	blood:	n/a	n/a
4	ATF3	chr7:103047287-103047672	A549	lung:	n/a	n/a
5	BHLHE40	chr7:103047241-103047730	K562	blood:	n/a	n/a
6	BHLHE40	chr7:103047235-103047716	HepG2	liver:	n/a	n/a
7	BHLHE40	chr7:103035429-103035549	K562	blood:	n/a	n/a
8	BHLHE40	chr7:103047337-103047568	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:103047285-103047647	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:103047305-103047520	HepG2	liver:	n/a	n/a
11	CBX3	chr7:103047194-103047798	K562	blood:	n/a	n/a
12	CBX3	chr7:103053858-103054252	K562	blood:	n/a	n/a
13	CBX3	chr7:103047153-103047771	HCT-116	colon:	n/a	n/a
14	CBX3	chr7:103053834-103054240	K562	blood:	n/a	n/a
15	CEBPB	chr7:103065348-103065482	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:103063934-103064280	A549	lung:	n/a	chr7:103064110-103064121
17	CEBPB	chr7:103031654-103032023	HepG2	liver:	n/a	chr7:103031841-103031852 chr7:103031841-103031854
18	CEBPB	chr7:103047406-103047764	K562	blood:	n/a	n/a
19	CEBPB	chr7:103060320-103060549	K562	blood:	n/a	n/a
20	CEBPB	chr7:103031656-103031978	K562	blood:	n/a	chr7:103031841-103031852 chr7:103031841-103031854
21	CEBPB	chr7:103031683-103031997	K562	blood:	n/a	chr7:103031841-103031852 chr7:103031841-103031854
22	CEBPB	chr7:103052745-103052864	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:103031677-103031931	A549	lung:	n/a	chr7:103031841-103031852 chr7:103031841-103031854
24	CEBPB	chr7:103063955-103064290	Hela-S3	cervix:	n/a	chr7:103064110-103064121
25	CEBPB	chr7:103061502-103062083	HepG2	liver:	n/a	chr7:103061718-103061730
26	CEBPB	chr7:103060146-103060343	HepG2	liver:	n/a	chr7:103060300-103060311
27	CEBPB	chr7:103063943-103064282	MCF-7	breast:	n/a	chr7:103064110-103064121
28	CEBPB	chr7:103063950-103064273	H1-hESC	embryonic stem cell:	n/a	chr7:103064110-103064121
29	CEBPB	chr7:103063937-103064281	IMR90	lung:	n/a	chr7:103064110-103064121
30	CEBPB	chr7:103063932-103064269	HepG2	liver:	n/a	chr7:103064110-103064121
31	CEBPB	chr7:103063911-103064242	K562	blood:	n/a	chr7:103064110-103064121
32	CEBPB	chr7:103063923-103064302	K562	blood:	n/a	chr7:103064110-103064121
33	CHD2	chr7:103047423-103047629	HepG2	liver:	n/a	n/a
34	CTCF	chr7:103065785-103065839	Gliobla	brain:	n/a	n/a
35	CTCF	chr7:103047440-103047590	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr7:103047420-103047570	GM12873	blood:	n/a	n/a
37	CTCF	chr7:103047377-103047576	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr7:103047440-103047590	GM12868	blood:	n/a	n/a
39	CTCF	chr7:103065800-103065950	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr7:103047460-103047610	HCFaa	heart:	n/a	n/a
41	CTCF	chr7:103065740-103065890	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:103047420-103047540	GM12891	blood:	n/a	n/a
43	CTCF	chr7:103065739-103065880	HepG2	liver:	n/a	n/a
44	CTCF	chr7:103055780-103055930	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr7:103047440-103047590	GM12867	blood:	n/a	n/a
46	CTCF	chr7:103047404-103047598	NHEK	skin:	n/a	n/a
47	CTCF	chr7:103047343-103047674	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr7:103047460-103047610	HPF	lung:	n/a	n/a
49	CTCF	chr7:103055140-103055290	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:103065721-103065927	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:103047436-103047486	SAEC	small airway:	n/a
2	chr7:103047436-103047486	SKMC	muscle:	n/a
3	chr7:103047436-103047486	BJ	skin:	n/a
4	chr7:103047436-103047486	HL-60	blood:	n/a
5	chr7:103047436-103047486	HUVEC	blood vessel:	n/a
6	chr7:103047436-103047486	SK-N-SH	brain:	n/a
7	chr7:103047436-103047486	IMR90	lung:	fetal
8	chr7:103047436-103047486	T-47D	breast:	n/a
9	chr7:103047436-103047486	GM06990	blood:	n/a
10	chr7:103047436-103047486	GM12891	blood:	n/a
11	chr7:103047436-103047486	NHDF-neo	bronchial:	n/a
12	chr7:103047436-103047486	AG04450	lung:	fetal
13	chr7:103047436-103047486	MCF-7	breast:	n/a
14	chr7:103047436-103047486	HAEpiC	amniotic membrane:	n/a
15	chr7:103047436-103047486	ECC-1	luminal epithelium:	n/a
16	chr7:103047436-103047486	GM12892	blood:	n/a
17	chr7:103047436-103047486	HRCEpiC	kidney:	n/a
18	chr7:103047436-103047486	Jurkat	blood:	n/a
19	chr7:103047436-103047486	MCF10A-Er-Src	breast:	n/a
20	chr7:103047436-103047486	NHBE	bronchial:	n/a
21	chr7:103047436-103047486	SK-N-MC	brain:	n/a
22	chr7:103047436-103047486	GM12878	blood:	n/a
23	chr7:103047436-103047486	PrEC	prostate:	n/a
24	chr7:103047436-103047486	BE2_C	brain:	n/a
25	chr7:103047436-103047486	H1-hESC	embryonic stem cell:	embryo
26	chr7:103047436-103047486	RPTEC	kidney:	n/a
27	chr7:103047436-103047486	PANC-1	pancreas:	n/a
28	chr7:103047436-103047486	ProgFib	skin:	n/a
29	chr7:103047436-103047486	HCPEpiC	choroid plexus:	n/a
30	chr7:103047436-103047486	HNPCEpiC	eye:	n/a
31	chr7:103047436-103047486	Hela-S3	cervix:	n/a
32	chr7:103047436-103047486	NT2-D1	testis:	n/a
33	chr7:103047436-103047486	HEEpiC	esophagus:	n/a
34	chr7:103047436-103047486	LNCaP	prostate:	n/a
35	chr7:103047436-103047486	AG10803	skin:	n/a
36	chr7:103047436-103047486	HEK293	kidney:	embryo
37	chr7:103047436-103047486	GM19239	blood:	n/a
38	chr7:103047436-103047486	HPAEpiC	pulmonary alveolar:	n/a
39	chr7:103047436-103047486	Hepatocyte	liver:	n/a
40	chr7:103047436-103047486	HCF	heart:	n/a
41	chr7:103047436-103047486	HMEC	breast:	n/a
42	chr7:103047436-103047486	PFSK-1	brain:	n/a
43	chr7:103047436-103047486	AG09309	skin:	n/a
44	chr7:103047436-103047486	HCM	heart:	n/a
45	chr7:103047436-103047486	Caco-2	colon:	n/a
46	chr7:103047436-103047486	A549	lung:	n/a
47	chr7:103047436-103047486	K562	blood:	n/a
48	chr7:103047436-103047486	AoSMC	blood vessel:	n/a
49	chr7:103047436-103047486	HRPEpiC	eye:	n/a
50	chr7:103047436-103047486	HIPEpiC	eye:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:103034064..103036544-chr7:103038634..103040596,2	K562	blood:
2	chr7:102936159..102939121-chr7:103047482..103049245,2	MCF-7	breast:
3	chr7:103031484..103034143-chr7:103051102..103054034,2	MCF-7	breast:
4	chr7:103064365..103066783-chr7:103071791..103075668,4	K562	blood:
5	chr7:103050674..103053630-chr7:103055786..103058061,2	MCF-7	breast:
6	chr7:103036875..103038919-chr7:103049967..103051484,2	K562	blood:
7	chr7:102984036..102986736-chr7:103049707..103052051,2	K562	blood:
8	chr7:103036875..103038919-chr7:103049967..103051484,2	K562	blood:
9	chr7:103050674..103053630-chr7:103055786..103058061,2	MCF-7	breast:
10	chr7:103007094..103009169-chr7:103030606..103033523,2	MCF-7	breast:
11	chr7:102936192..102939574-chr7:103045971..103049188,7	MCF-7	breast:
12	chr7:102937267..102938325-chr7:103047048..103048128,12	K562	blood:
13	chr7:102936749..102940052-chr7:103045888..103048510,5	K562	blood:
14	chr12:120727150..120729921-chr7:103064420..103066581,2	MCF-7	breast:
15	chr7:102616176..102618073-chr7:103034545..103036072,2	K562	blood:
16	chr7:103030653..103032689-chr7:104652103..104653783,2	MCF-7	breast:
17	chr7:103029058..103031170-chr7:103031992..103033523,2	K562	blood:
18	chr7:103066919..103068648-chr7:103073058..103076029,2	MCF-7	breast:
19	chr7:102987552..102990290-chr7:103045935..103048754,2	K562	blood:
20	chr7:103031484..103034143-chr7:103051102..103054034,2	MCF-7	breast:
21	chr7:103034064..103036591-chr7:103039096..103041325,2	K562	blood:
22	chr7:102965490..102966174-chr7:103046992..103047933,2	MCF-7	breast:
23	chr7:102936159..102939401-chr7:103049478..103052861,5	MCF-7	breast:
24	chr7:102937314..102938229-chr7:103047003..103048135,8	MCF-7	breast:
25	chr7:103010338..103013174-chr7:103051030..103053015,2	K562	blood:
26	chr7:102983601..102985754-chr7:103032135..103034382,3	MCF-7	breast:
27	chr7:102983782..102986600-chr7:103030812..103033916,3	MCF-7	breast:
28	chr7:103060391..103062412-chr7:103064074..103067234,3	K562	blood:
29	chr7:103064368..103066846-chr7:103068610..103071577,2	K562	blood:
30	chr7:102985801..102988049-chr7:103030466..103032133,2	K562	blood:
31	chr7:103017075..103019206-chr7:103029655..103032336,2	MCF-7	breast:
32	chr7:102723533..102726429-chr7:103048128..103049854,2	K562	blood:
33	chr7:102936688..102939206-chr7:103050065..103051643,2	K562	blood:
34	chr7:103034064..103036591-chr7:103039096..103041325,2	K562	blood:
35	chr7:102937571..102939280-chr7:103063812..103065320,2	K562	blood:
36	chr7:103034064..103036544-chr7:103038634..103040596,2	K562	blood:
37	chr7:102937436..102938311-chr7:103047038..103047999,8	MCF-7	breast:

No data

Variant related genes	Relation type
SLC26A5	TF binding region
SLC26A5	CpG island
ENSG00000235354	chromatin interactions
ENSG00000252047	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000251852	chromatin interactions
ENSG00000105821	chromatin interactions
ENSG00000161057	chromatin interactions
ENSG00000170615	chromatin interactions
ENSG00000105819	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 1121 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1121 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539747085	chr7:103031838-103031839	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs187441939	chr7:103031920-103031921	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs74584081	chr7:103031926-103031927	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs141799711	chr7:103031931-103031932	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs567844061	chr7:103031949-103031950	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs113284781	chr7:103031953-103031954	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112744367	chr7:103031980-103031981	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs191459658	chr7:103032055-103032056	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs150033360	chr7:103032060-103032061	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs368745441	chr7:103032071-103032072	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs557612359	chr7:103032072-103032073	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs562854182	chr7:103032076-103032077	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs372387853	chr7:103032083-103032084	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs199803319	chr7:103032084-103032085	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs555983287	chr7:103032125-103032126	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs576599754	chr7:103032137-103032138	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs376409779	chr7:103032191-103032192	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs369654344	chr7:103032220-103032221	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs530195379	chr7:103032230-103032231	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs55793035	chr7:103032238-103032239	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs182420611	chr7:103032272-103032273	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs145530831	chr7:103032325-103032326	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs541460029	chr7:103032354-103032355	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs112212960	chr7:103032383-103032384	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs559862041	chr7:103032387-103032388	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs148844936	chr7:103032390-103032391	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs187461659	chr7:103032408-103032409	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs563444236	chr7:103032416-103032417	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs55801500	chr7:103032439-103032440	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs192009313	chr7:103032469-103032470	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs564452530	chr7:103032526-103032527	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs528053655	chr7:103032532-103032533	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs546224735	chr7:103032573-103032574	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs369494127	chr7:103032575-103032576	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs10155812	chr7:103032603-103032604	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs367630735	chr7:103032645-103032646	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs527362596	chr7:103032656-103032657	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs529114092	chr7:103032688-103032689	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs376742376	chr7:103032689-103032690	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs550266304	chr7:103032751-103032752	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183412765	chr7:103032797-103032798	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs372890523	chr7:103032824-103032825	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs75044386	chr7:103032853-103032854	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs76883807	chr7:103032860-103032861	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs568255907	chr7:103032877-103032878	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs78920112	chr7:103032887-103032888	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373064048	chr7:103032930-103032931	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572767093	chr7:103033002-103033003	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs189035240	chr7:103033036-103033037	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs553370965	chr7:103033039-103033040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	21147910	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103022600-103033200	Weak transcription	Gastric	stomach
2	chr7:103029400-103032800	Enhancers	Stomach Mucosa	stomach
3	chr7:103029800-103032000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:103030000-103032400	Enhancers	HepG2	liver
5	chr7:103032000-103032800	Enhancers	Duodenum Mucosa	Duodenum
6	chr7:103032800-103033000	Flanking Active TSS	K562	blood
7	chr7:103032800-103033200	Weak transcription	Stomach Mucosa	stomach
8	chr7:103032800-103038800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr7:103033000-103033600	Enhancers	K562	blood
10	chr7:103033200-103034400	Enhancers	Gastric	stomach
11	chr7:103033200-103037200	Enhancers	Stomach Mucosa	stomach
12	chr7:103033600-103035200	Weak transcription	K562	blood
13	chr7:103034400-103035000	Weak transcription	Gastric	stomach
14	chr7:103035000-103035200	Enhancers	Aorta	Aorta
15	chr7:103035000-103035600	Enhancers	Gastric	stomach
16	chr7:103035200-103035600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:103035200-103037000	Enhancers	K562	blood
18	chr7:103035600-103036400	Weak transcription	Gastric	stomach
19	chr7:103036400-103036600	Enhancers	Gastric	stomach
20	chr7:103036800-103037200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr7:103036800-103037200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:103037200-103038800	Weak transcription	Stomach Mucosa	stomach
23	chr7:103038800-103039200	Enhancers	HepG2	liver
24	chr7:103038800-103039400	Enhancers	Stomach Mucosa	stomach
25	chr7:103038800-103040000	Enhancers	Duodenum Mucosa	Duodenum
26	chr7:103044600-103046800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:103045800-103046600	Enhancers	HepG2	liver
28	chr7:103046000-103047400	Enhancers	Stomach Mucosa	stomach
29	chr7:103046400-103047200	Enhancers	Liver	Liver
30	chr7:103046600-103046800	Weak transcription	Gastric	stomach
31	chr7:103046600-103046800	Flanking Active TSS	HepG2	liver
32	chr7:103046600-103047000	Enhancers	K562	blood
33	chr7:103046600-103047600	Enhancers	GM12878-XiMat	blood
34	chr7:103046800-103047000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:103046800-103047000	Enhancers	Gastric	stomach
36	chr7:103046800-103047600	Enhancers	HepG2	liver
37	chr7:103046800-103047800	Enhancers	Duodenum Mucosa	Duodenum
38	chr7:103047000-103047400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:103047000-103047400	Flanking Active TSS	K562	blood
40	chr7:103047000-103053800	Weak transcription	Gastric	stomach
41	chr7:103047200-103047600	Enhancers	Brain Substantia Nigra	brain
42	chr7:103047200-103047600	Active TSS	A549	lung
43	chr7:103047200-103048000	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr7:103047400-103047600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:103047400-103047800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:103047400-103048400	Enhancers	K562	blood
47	chr7:103047400-103053000	Weak transcription	Stomach Mucosa	stomach
48	chr7:103047600-103047800	Enhancers	Brain Anterior Caudate	brain
49	chr7:103048400-103051800	Weak transcription	K562	blood
50	chr7:103051800-103052000	Enhancers	K562	blood

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