Variant report

Variant	esv3436506
Chromosome Location	chr7:100291316-100292864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:100291896-100292366	H1-hESC	embryonic stem cell:	n/a	chr7:100292108-100292117
2	ATF3	chr7:100291721-100292277	HepG2	liver:	n/a	chr7:100291894-100291914 chr7:100292108-100292117
3	ATF3	chr7:100292007-100292275	GM12878	blood:	n/a	chr7:100292108-100292117
4	ATF3	chr7:100291794-100291938	K562	blood:	n/a	chr7:100291894-100291914
5	ATF3	chr7:100292020-100292321	H1-hESC	embryonic stem cell:	n/a	chr7:100292108-100292117
6	ATF3	chr7:100291810-100291931	GM12878	blood:	n/a	chr7:100291894-100291914
7	ATF3	chr7:100291966-100292343	K562	blood:	n/a	chr7:100292108-100292117
8	ATF3	chr7:100291793-100292401	GM12878	blood:	n/a	chr7:100291894-100291914 chr7:100292108-100292117
9	ATF3	chr7:100291987-100292415	HepG2	liver:	n/a	chr7:100292108-100292117
10	BHLHE40	chr7:100291863-100292368	GM12878	blood:	n/a	chr7:100292015-100292031
11	BHLHE40	chr7:100291857-100292379	K562	blood:	n/a	chr7:100292015-100292031
12	BHLHE40	chr7:100291993-100292228	HepG2	liver:	n/a	chr7:100292015-100292031
13	BHLHE40	chr7:100291873-100292385	HepG2	liver:	n/a	chr7:100292015-100292031
14	CBX3	chr7:100292104-100292379	K562	blood:	n/a	n/a
15	CBX3	chr7:100291959-100292699	K562	blood:	n/a	n/a
16	CCNT2	chr7:100291240-100292343	K562	blood:	n/a	chr7:100291296-100291305 chr7:100292209-100292218
17	CEBPD	chr7:100291957-100292347	HepG2	liver:	n/a	n/a
18	CHD1	chr7:100291458-100291513	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr7:100291449-100291472	GM12878	blood:	n/a	n/a
20	CHD2	chr7:100292011-100292341	Hela-S3	cervix:	n/a	chr7:100292203-100292213 chr7:100292106-100292116
21	CHD2	chr7:100292154-100292332	K562	blood:	n/a	chr7:100292203-100292213
22	CREB1	chr7:100291660-100292400	HepG2	liver:	n/a	n/a
23	CREB1	chr7:100291702-100292332	A549	lung:	n/a	n/a
24	CTCF	chr7:100291254-100291329	GM10266	blood:	n/a	chr7:100291304-100291317
25	CTCF	chr7:100291360-100291510	GM12865	blood:	n/a	n/a
26	CTCF	chr7:100291180-100291330	Caco-2	colon:	n/a	chr7:100291304-100291317
27	CTCF	chr7:100291200-100291350	RPTEC	kidney:	n/a	chr7:100291304-100291317
28	CTCF	chr7:100292534-100292552	Lung_OC	lung:	n/a	n/a
29	CTCF	chr7:100291837-100291868	GM19239	blood:	n/a	n/a
30	CTCF	chr7:100291200-100291350	AG09319	gingival:	n/a	chr7:100291304-100291317
31	CTCF	chr7:100291180-100291330	HMEC	breast:	n/a	chr7:100291304-100291317
32	CTCF	chr7:100288330-100291509	SK-N-SH	brain:	n/a	chr7:100289445-100289463 chr7:100289242-100289255 chr7:100289447-100289460 chr7:100291304-100291317 chr7:100289217-100289230 chr7:100288748-100288756 chr7:100289440-100289461
33	CTCFL	chr7:100292052-100292212	K562	blood:	n/a	n/a
34	E2F1	chr7:100291340-100292204	Hela-S3	cervix:	n/a	chr7:100291512-100291522 chr7:100291534-100291546 chr7:100291514-100291523 chr7:100291416-100291426
35	E2F4	chr7:100291805-100292313	K562	blood:	n/a	n/a
36	E2F4	chr7:100292190-100292375	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F6	chr7:100291256-100292341	K562	blood:	n/a	chr7:100291512-100291522 chr7:100291534-100291546 chr7:100291514-100291523 chr7:100291416-100291426
38	E2F6	chr7:100291815-100292371	H1-hESC	embryonic stem cell:	n/a	n/a
39	E2F6	chr7:100291992-100292360	Hela-S3	cervix:	n/a	n/a
40	E2F6	chr7:100291832-100292525	H1-hESC	embryonic stem cell:	n/a	n/a
41	E2F6	chr7:100291988-100292411	A549	lung:	n/a	n/a
42	E2F6	chr7:100291798-100292599	A549	lung:	n/a	n/a
43	E2F6	chr7:100291452-100292320	K562	blood:	n/a	chr7:100291512-100291522 chr7:100291534-100291546 chr7:100291514-100291523
44	E2F6	chr7:100291830-100292400	K562	blood:	n/a	n/a
45	EBF1	chr7:100292129-100292341	GM12878	blood:	n/a	n/a
46	EGR1	chr7:100292079-100292280	GM12878	blood:	n/a	chr7:100292201-100292215 chr7:100292245-100292255 chr7:100292099-100292109
47	EGR1	chr7:100291231-100291461	GM12878	blood:	n/a	chr7:100291361-100291375 chr7:100291360-100291373 chr7:100291275-100291285 chr7:100291358-100291368 chr7:100291360-100291373 chr7:100291363-100291372 chr7:100291360-100291373
48	EGR1	chr7:100291995-100292357	K562	blood:	n/a	chr7:100292201-100292215 chr7:100292245-100292255 chr7:100292099-100292109
49	EGR1	chr7:100291559-100291908	GM12878	blood:	n/a	chr7:100291760-100291774
50	EGR1	chr7:100291985-100292382	K562	blood:	n/a	chr7:100292201-100292215 chr7:100292245-100292255 chr7:100292099-100292109

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100292329-100292379	NHBE	bronchial:	n/a
2	chr7:100292329-100292379	NHBE	bronchial:	n/a
3	chr7:100292265-100292315	Caco-2	colon:	n/a
4	chr7:100291891-100291941	MCF-7	breast:	n/a
5	chr7:100291438-100291488	ProgFib	skin:	n/a
6	chr7:100291891-100291941	AG04450	lung:	fetal
7	chr7:100292329-100292379	HRCEpiC	kidney:	n/a
8	chr7:100291891-100291941	AG09309	skin:	n/a
9	chr7:100292329-100292379	HRE	kidney:	n/a
10	chr7:100291891-100291941	SK-N-MC	brain:	n/a
11	chr7:100291848-100291898	RPTEC	kidney:	n/a
12	chr7:100291905-100291955	SKMC	muscle:	n/a
13	chr7:100292329-100292379	HNPCEpiC	eye:	n/a
14	chr7:100291848-100291898	SK-N-MC	brain:	n/a
15	chr7:100291848-100291898	HUVEC	blood vessel:	n/a
16	chr7:100291438-100291488	AG09319	gingival:	n/a
17	chr7:100291891-100291941	GM12892	blood:	n/a
18	chr7:100291891-100291941	HMEC	breast:	n/a
19	chr7:100292329-100292379	MCF-7	breast:	n/a
20	chr7:100291848-100291898	MCF10A-Er-Src	breast:	n/a
21	chr7:100291891-100291941	HepG2	liver:	n/a
22	chr7:100291848-100291898	U87	brain:	n/a
23	chr7:100291438-100291488	Hepatocyte	liver:	n/a
24	chr7:100291438-100291488	RPTEC	kidney:	n/a
25	chr7:100291438-100291488	LNCaP	prostate:	n/a
26	chr7:100292329-100292379	HUVEC	blood vessel:	n/a
27	chr7:100292329-100292379	HAEpiC	amniotic membrane:	n/a
28	chr7:100292329-100292379	HCT-116	colon:	n/a
29	chr7:100291905-100291955	HepG2	liver:	n/a
30	chr7:100291891-100291941	CMK	blood:	n/a
31	chr7:100292265-100292315	Hepatocyte	liver:	n/a
32	chr7:100292265-100292315	BJ	skin:	n/a
33	chr7:100291905-100291955	HRE	kidney:	n/a
34	chr7:100292329-100292379	IMR90	lung:	fetal
35	chr7:100291438-100291488	ECC-1	luminal epithelium:	n/a
36	chr7:100291438-100291488	HMEC	breast:	n/a
37	chr7:100292265-100292315	HNPCEpiC	eye:	n/a
38	chr7:100291848-100291898	SK-N-SH	brain:	n/a
39	chr7:100291905-100291955	ProgFib	skin:	n/a
40	chr7:100291891-100291941	SK-N-SH	brain:	n/a
41	chr7:100292329-100292379	HCF	heart:	n/a
42	chr7:100291905-100291955	BE2_C	brain:	n/a
43	chr7:100291905-100291955	Hepatocyte	liver:	n/a
44	chr7:100291438-100291488	GM12878	blood:	n/a
45	chr7:100291905-100291955	HIPEpiC	eye:	n/a
46	chr7:100291905-100291955	HRPEpiC	eye:	n/a
47	chr7:100291848-100291898	GM06990	blood:	n/a
48	chr7:100292329-100292379	SK-N-SH	brain:	n/a
49	chr7:100291848-100291898	Hepatocyte	liver:	n/a
50	chr7:100291905-100291955	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:100068696..100070699-chr7:100288610..100291361,2	MCF-7	breast:
2	chr7:100291635..100293380-chr7:100321369..100322955,2	MCF-7	breast:
3	chr7:100162910..100168606-chr7:100287546..100292436,6	MCF-7	breast:
4	chr7:100290034..100292271-chr7:100471770..100473597,2	MCF-7	breast:
5	chr7:100207033..100212293-chr7:100287661..100294075,8	MCF-7	breast:
6	chr7:100291734..100293834-chr7:100411313..100413984,2	MCF-7	breast:
7	chr7:100289314..100293442-chr7:100296051..100298941,4	MCF-7	breast:
8	chr7:100239190..100240878-chr7:100289804..100292344,2	MCF-7	breast:
9	chr7:100208850..100211238-chr7:100289549..100292875,4	K562	blood:
10	chr7:100291258..100294008-chr7:100480725..100482428,2	MCF-7	breast:
11	chr7:100144116..100146517-chr7:100289943..100291876,2	K562	blood:
12	chr7:100184159..100186286-chr7:100289610..100292155,2	MCF-7	breast:
13	chr7:100031056..100033045-chr7:100289882..100292059,2	K562	blood:
14	chr7:100288252..100292867-chr7:100319528..100322364,4	K562	blood:
15	chr7:100181942..100185382-chr7:100289663..100293010,6	K562	blood:
16	chr7:100177845..100180104-chr7:100290366..100293709,4	MCF-7	breast:
17	chr7:100179120..100183907-chr7:100289595..100293366,6	MCF-7	breast:
18	chr7:100288992..100293891-chr7:100317292..100321001,4	MCF-7	breast:
19	chr7:100197481..100201934-chr7:100289981..100293981,6	MCF-7	breast:
20	chr7:100290419..100293382-chr7:100421709..100425907,4	MCF-7	breast:
21	chr7:100289903..100293307-chr7:100301970..100305114,7	K562	blood:
22	chr7:100288044..100289593-chr7:100290175..100291688,2	K562	blood:
23	chr7:100199658..100204753-chr7:100287607..100293733,10	K562	blood:
24	chr20:47894371..47895084-chr7:100291569..100292239,2	HCT-116	colon:
25	chr7:100025034..100028922-chr7:100288914..100292951,6	K562	blood:
26	chr7:100034415..100037250-chr7:100289483..100291820,2	MCF-7	breast:
27	chr7:100289903..100293628-chr7:100299918..100304988,11	K562	blood:
28	chr7:100198433..100204411-chr7:100285757..100293733,14	K562	blood:
29	chr7:100290049..100291654-chr7:100463321..100465099,2	MCF-7	breast:
30	chr6:26053433..26055851-chr7:100290372..100293044,2	MCF-7	breast:
31	chr7:100292109..100293642-chr7:100462189..100464679,2	MCF-7	breast:
32	chr7:100080135..100081654-chr7:100290333..100292892,2	MCF-7	breast:
33	chr7:100025861..100030068-chr7:100288797..100293203,7	K562	blood:
34	chr7:100288390..100292044-chr7:100484527..100487788,3	MCF-7	breast:
35	chr7:100289891..100291847-chr7:100416190..100417802,2	K562	blood:
36	chr7:100183057..100185845-chr7:100291476..100293682,3	MCF-7	breast:
37	chr7:100247255..100249496-chr7:100290650..100293134,2	K562	blood:
38	chr7:100180869..100184882-chr7:100287482..100291355,9	MCF-7	breast:
39	chr7:100287688..100293699-chr7:100300603..100306359,15	MCF-7	breast:
40	chr7:100222794..100225924-chr7:100289657..100292852,4	MCF-7	breast:
41	chr7:100254369..100255974-chr7:100290427..100292129,2	K562	blood:

Variant related genes	Relation type
GIGYF1	TF binding region
GIGYF1	CpG island
ENSG00000266372	chromatin interactions
ENSG00000241357	chromatin interactions
ENSG00000172336	chromatin interactions
ENSG00000146828	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000224729	chromatin interactions
ENSG00000077454	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000176125	chromatin interactions
ENSG00000106330	chromatin interactions
ENSG00000087077	chromatin interactions
ENSG00000166924	chromatin interactions
ENSG00000087087	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000106333	chromatin interactions
ENSG00000106327	chromatin interactions
ENSG00000130427	chromatin interactions
ENSG00000106336	chromatin interactions
ENSG00000196411	chromatin interactions
ENSG00000184414	chromatin interactions

Extended variants
information (count: 37 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113750037	chr7:100291460-100291461	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
2	rs186622817	chr7:100291485-100291486	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
3	rs113371859	chr7:100291615-100291616	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
4	rs191319537	chr7:100291636-100291637	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
5	rs183181389	chr7:100291702-100291703	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
6	rs200727756	chr7:100291793-100291794	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
7	rs188458074	chr7:100291827-100291828	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
8	rs546108497	chr7:100291828-100291829	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
9	rs545497452	chr7:100291832-100291833	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
10	rs557892428	chr7:100292068-100292069	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
11	rs368401424	chr7:100292098-100292099	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
12	rs58547229	chr7:100292195-100292196	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
13	rs61422411	chr7:100292197-100292198	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
14	rs573402016	chr7:100292203-100292204	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
15	rs540720795	chr7:100292213-100292214	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
16	rs372715918	chr7:100292291-100292292	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
17	rs59197513	chr7:100292355-100292356	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
18	rs562071431	chr7:100292418-100292419	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
19	rs529272456	chr7:100292420-100292421	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
20	rs193032161	chr7:100292434-100292435	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
21	rs183384925	chr7:100292498-100292499	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
22	rs188079002	chr7:100292523-100292524	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
23	rs192490352	chr7:100292529-100292530	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
24	rs568964846	chr7:100292538-100292539	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
25	rs183929816	chr7:100292570-100292571	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
26	rs7804078	chr7:100292623-100292624	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs528321846	chr7:100292634-100292635	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
28	rs546653242	chr7:100292635-100292636	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs147776497	chr7:100292673-100292674	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs568095323	chr7:100292682-100292683	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs535187804	chr7:100292697-100292698	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs560749934	chr7:100292705-100292706	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs112119547	chr7:100292706-100292707	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs568514352	chr7:100292724-100292725	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs528030314	chr7:100292748-100292749	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs539736666	chr7:100292765-100292766	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs221784	chr7:100292830-100292831	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	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
Acute lymphoblastic leukemia	21339820	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
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100289400-100291400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr7:100289400-100291600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
3	chr7:100289600-100291600	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr7:100289600-100291600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:100289800-100291600	Flanking Active TSS	Primary hematopoietic stem cells	blood
6	chr7:100289800-100293600	Active TSS	H9 Cell Line	embryonic stem cell
7	chr7:100290000-100293800	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr7:100290400-100291400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr7:100290400-100291400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
10	chr7:100290400-100291400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr7:100290400-100291600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:100290400-100291600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
13	chr7:100290400-100292600	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr7:100290600-100291600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr7:100290600-100291600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:100290600-100291600	Active TSS	GM12878-XiMat	blood
17	chr7:100290600-100291800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:100290600-100292400	Active TSS	H1 Cell Line	embryonic stem cell
19	chr7:100290600-100292400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:100290600-100292400	Active TSS	Lung	lung
21	chr7:100290600-100292600	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr7:100290600-100292600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:100290600-100292600	Active TSS	Aorta	Aorta
24	chr7:100290600-100293600	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr7:100290600-100294000	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr7:100290800-100291400	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr7:100290800-100291400	Flanking Active TSS	Primary B cells from peripheral blood	blood
28	chr7:100290800-100291400	Active TSS	Fetal Brain Female	brain
29	chr7:100290800-100291400	Active TSS	Fetal Kidney	kidney
30	chr7:100290800-100291600	Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr7:100290800-100291600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:100290800-100291600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:100290800-100291600	Active TSS	Brain Cingulate Gyrus	brain
34	chr7:100290800-100291600	Active TSS	Fetal Intestine Large	intestine
35	chr7:100290800-100291600	Active TSS	Placenta Amnion	Placenta Amnion
36	chr7:100290800-100291600	Active TSS	A549	lung
37	chr7:100290800-100291600	Active TSS	K562	blood
38	chr7:100290800-100291600	Active TSS	NHDF-Ad	bronchial
39	chr7:100290800-100291600	Active TSS	NHEK	skin
40	chr7:100290800-100291600	Active TSS	NHLF	lung
41	chr7:100290800-100291800	Active TSS	Gastric	stomach
42	chr7:100290800-100292200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr7:100290800-100292200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:100290800-100292200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:100290800-100292200	Active TSS	Fetal Stomach	stomach
46	chr7:100290800-100292200	Active TSS	Osteobl	bone
47	chr7:100290800-100292400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr7:100290800-100292400	Active TSS	Muscle Satellite Cultured Cells	--
49	chr7:100290800-100292400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr7:100290800-100292400	Active TSS	Left Ventricle	heart

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