Variant report

Variant	esv1827496
Chromosome Location	chr7:99566264-99634782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2697)
CpG islands
(count:2566)
Chromatin interactive
region (count:159)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2697 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99588561-99588855	K562	blood:	n/a	n/a
2	ARID3A	chr7:99634317-99634961	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:99613002-99613272	K562	blood:	n/a	n/a
4	ARID3A	chr7:99621722-99621985	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:99595227-99595537	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:99601325-99601936	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:99573511-99574236	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:99610285-99610671	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:99578392-99578401	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:99588540-99588839	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:99591808-99592148	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:99612999-99613317	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:99591850-99592144	K562	blood:	n/a	n/a
14	ARID3A	chr7:99577288-99577300	K562	blood:	n/a	n/a
15	ARID3A	chr7:99614020-99614567	HepG2	liver:	n/a	n/a
16	ATF1	chr7:99613008-99613355	K562	blood:	n/a	n/a
17	ATF2	chr7:99595132-99595501	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr7:99612922-99613352	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr7:99595114-99595627	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr7:99612925-99613402	GM12878	blood:	n/a	n/a
21	ATF2	chr7:99588414-99588699	GM12878	blood:	n/a	n/a
22	ATF2	chr7:99623674-99624169	GM12878	blood:	n/a	n/a
23	ATF2	chr7:99588383-99588853	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr7:99612938-99613479	K562	blood:	n/a	n/a
25	ATF3	chr7:99588519-99588908	A549	lung:	n/a	n/a
26	ATF3	chr7:99612906-99613380	A549	lung:	n/a	n/a
27	BACH1	chr7:99612991-99613276	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:99588600-99588743	K562	blood:	n/a	n/a
29	BATF	chr7:99623746-99624108	GM12878	blood:	n/a	chr7:99623935-99623946
30	BATF	chr7:99623677-99624143	GM12878	blood:	n/a	chr7:99623935-99623946
31	BATF	chr7:99612974-99613349	GM12878	blood:	n/a	n/a
32	BCL3	chr7:99612943-99613384	A549	lung:	n/a	chr7:99613205-99613214
33	BCL3	chr7:99612971-99613328	GM12878	blood:	n/a	chr7:99613205-99613214
34	BCLAF1	chr7:99612943-99613345	GM12878	blood:	n/a	chr7:99613205-99613214
35	BCLAF1	chr7:99623673-99624175	GM12878	blood:	n/a	n/a
36	BCLAF1	chr7:99612895-99613380	GM12878	blood:	n/a	chr7:99613205-99613214
37	BCLAF1	chr7:99595032-99595589	GM12878	blood:	n/a	chr7:99595317-99595326
38	BHLHE40	chr7:99612987-99613358	K562	blood:	n/a	n/a
39	BHLHE40	chr7:99576876-99576892	K562	blood:	n/a	n/a
40	BHLHE40	chr7:99621688-99622047	HepG2	liver:	n/a	n/a
41	BHLHE40	chr7:99623878-99624027	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:99595201-99595644	HepG2	liver:	n/a	n/a
43	BHLHE40	chr7:99573751-99574031	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:99591934-99592020	K562	blood:	n/a	n/a
45	BHLHE40	chr7:99595199-99595648	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:99577501-99577734	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:99588564-99588813	K562	blood:	n/a	n/a
48	BHLHE40	chr7:99601366-99601918	HepG2	liver:	n/a	n/a
49	BHLHE40	chr7:99577510-99577734	K562	blood:	n/a	n/a
50	BRCA1	chr7:99601493-99601826	HepG2	liver:	n/a	n/a

(count:2566 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99630899-99630949	MCF-7	breast:	n/a
2	chr7:99598775-99598825	NB4	blood:	n/a
3	chr7:99576547-99576597	SAEC	small airway:	n/a
4	chr7:99631485-99631535	SK-N-SH	brain:	n/a
5	chr7:99630899-99630949	MCF-7	breast:	n/a
6	chr7:99598775-99598825	NB4	blood:	n/a
7	chr7:99576547-99576597	SAEC	small airway:	n/a
8	chr7:99631485-99631535	SK-N-SH	brain:	n/a
9	chr7:99627985-99628035	GM06990	blood:	n/a
10	chr7:99613244-99613294	HRPEpiC	eye:	n/a
11	chr7:99595658-99595708	HRPEpiC	eye:	n/a
12	chr7:99627985-99628035	HRCEpiC	kidney:	n/a
13	chr7:99630979-99631029	GM12892	blood:	n/a
14	chr7:99613244-99613294	HNPCEpiC	eye:	n/a
15	chr7:99613205-99613255	HRCEpiC	kidney:	n/a
16	chr7:99574466-99574516	SAEC	small airway:	n/a
17	chr7:99595458-99595508	GM06990	blood:	n/a
18	chr7:99613244-99613294	GM12878	blood:	n/a
19	chr7:99614209-99614259	PrEC	prostate:	n/a
20	chr7:99588335-99588385	Hepatocyte	liver:	n/a
21	chr7:99574383-99574433	AG04450	lung:	fetal
22	chr7:99591962-99592012	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:99588561-99588611	HL-60	blood:	n/a
24	chr7:99573278-99573328	ProgFib	skin:	n/a
25	chr7:99616820-99616870	NH-A	brain:	n/a
26	chr7:99576547-99576597	PANC-1	pancreas:	n/a
27	chr7:99595437-99595487	LNCaP	prostate:	n/a
28	chr7:99588561-99588611	U87	brain:	n/a
29	chr7:99613517-99613567	SKMC	muscle:	n/a
30	chr7:99612715-99612765	AoSMC	blood vessel:	n/a
31	chr7:99630979-99631029	SKMC	muscle:	n/a
32	chr7:99576547-99576597	NHBE	bronchial:	n/a
33	chr7:99613192-99613242	T-47D	breast:	n/a
34	chr7:99613205-99613255	HIPEpiC	eye:	n/a
35	chr7:99598775-99598825	GM12891	blood:	n/a
36	chr7:99613205-99613255	HCPEpiC	choroid plexus:	n/a
37	chr7:99616820-99616870	MCF10A-Er-Src	breast:	n/a
38	chr7:99632812-99632862	SK-N-SH	brain:	n/a
39	chr7:99576539-99576589	NHBE	bronchial:	n/a
40	chr7:99598775-99598825	HL-60	blood:	n/a
41	chr7:99613147-99613197	U87	brain:	n/a
42	chr7:99587136-99587186	K562	blood:	n/a
43	chr7:99573278-99573328	CMK	blood:	n/a
44	chr7:99588273-99588323	Hepatocyte	liver:	n/a
45	chr7:99595458-99595508	AG09309	skin:	n/a
46	chr7:99630899-99630949	ECC-1	luminal epithelium:	n/a
47	chr7:99587136-99587186	GM12892	blood:	n/a
48	chr7:99595276-99595326	HMEC	breast:	n/a
49	chr7:99612634-99612684	RPTEC	kidney:	n/a
50	chr7:99630998-99631048	IMR90	lung:	fetal

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:99590363..99592421-chr7:99597136..99600060,2	MCF-7	breast:
2	chr7:99600850..99603029-chr7:99645305..99648884,3	K562	blood:
3	chr19:55918691..55919435-chr7:99612825..99613381,2	HCT-116	colon:
4	chr1:45196470..45197118-chr7:99613158..99613683,2	Hela-S3	cervix:
5	chr7:99586340..99588249-chr7:99590043..99591844,2	K562	blood:
6	chr7:99600014..99604498-chr7:99605032..99608017,4	MCF-7	breast:
7	chr7:99510472..99511406-chr7:99588187..99589134,5	K562	blood:
8	chr7:99612024..99615373-chr7:99646672..99650813,5	MCF-7	breast:
9	chr7:99626508..99630728-chr7:99630857..99634217,6	MCF-7	breast:
10	chr7:99514062..99516474-chr7:99604675..99606310,2	MCF-7	breast:
11	chr7:99618314..99620224-chr7:99678750..99680788,2	MCF-7	breast:
12	chr7:99589288..99591810-chr7:99612834..99614804,4	MCF-7	breast:
13	chr7:99228995..99229922-chr7:99588200..99589102,3	K562	blood:
14	chr7:99591475..99592458-chr7:99650846..99651525,3	MCF-7	breast:
15	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
16	chr7:99604525..99607316-chr7:99612606..99614648,4	MCF-7	breast:
17	chr7:99577230..99578015-chr7:99588605..99589135,2	MCF-7	breast:
18	chr7:99516539..99518815-chr7:99613011..99615072,3	K562	blood:
19	chr7:99626268..99629732-chr7:99646321..99649999,3	MCF-7	breast:
20	chr7:99600927..99603522-chr7:99678013..99680469,2	MCF-7	breast:
21	chr7:99611956..99613934-chr7:99634714..99636555,2	K562	blood:
22	chr7:99627608..99629341-chr7:99632124..99633750,2	K562	blood:
23	chr7:99528952..99531320-chr7:99615014..99616984,2	K562	blood:
24	chr7:99598705..99603395-chr7:99611992..99615824,4	MCF-7	breast:
25	chr7:99612275..99615910-chr7:99677885..99681193,8	K562	blood:
26	chr7:99611884..99615327-chr7:99716112..99720187,5	K562	blood:
27	chr7:99626508..99630728-chr7:99630857..99634217,6	MCF-7	breast:
28	chr7:99601762..99603433-chr7:99603449..99606278,2	K562	blood:
29	chr7:99616524..99619632-chr7:99677690..99679745,3	K562	blood:
30	chr7:99601351..99605536-chr7:99611061..99616564,8	K562	blood:
31	chr7:99627608..99629341-chr7:99632124..99633750,2	K562	blood:
32	chr7:99618852..99620390-chr7:99647489..99649484,2	MCF-7	breast:
33	chr7:99626985..99629362-chr7:99630323..99632638,2	MCF-7	breast:
34	chr7:99626985..99629362-chr7:99630323..99632638,2	MCF-7	breast:
35	chr16:56966049..56966601-chr7:99612783..99613720,2	NB4	blood:
36	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
37	chr7:99595238..99600680-chr7:99611222..99614830,6	K562	blood:
38	chr7:99626222..99628459-chr7:99637263..99639191,3	MCF-7	breast:
39	chr7:99591337..99592929-chr7:99646894..99648865,2	MCF-7	breast:
40	chr7:99509274..99509946-chr7:99588276..99588980,2	MCF-7	breast:
41	chr7:99582037..99584694-chr7:99677705..99680267,2	K562	blood:
42	chr7:99590363..99592421-chr7:99597136..99600060,2	MCF-7	breast:
43	chr7:99623016..99624978-chr7:99629565..99632426,3	K562	blood:
44	chr7:99588806..99591548-chr7:99620634..99622161,2	MCF-7	breast:
45	chr7:99577524..99578039-chr7:99588237..99589217,3	K562	blood:
46	chr7:99611817..99614127-chr7:99645173..99647750,3	K562	blood:
47	chr7:99580447..99583544-chr7:99586500..99589317,4	K562	blood:
48	chr7:99601356..99603407-chr7:99644840..99648336,3	MCF-7	breast:
49	chr7:99600081..99603641-chr7:99645981..99649088,4	MCF-7	breast:
50	chr7:99591473..99592533-chr7:99642040..99642986,5	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZKSCAN1-1	chr7:99608999-99609247	XLOC_006188
2	lnc-ZKSCAN1-1	chr7:99597123-99597186	XLOC_006188
3	lnc-ZKSCAN1-1	chr7:99606205-99606730	XLOC_006188
4	lnc-ZKSCAN1-1	chr7:99605744-99605862	XLOC_006188
5	lnc-ZKSCAN1-1	chr7:99597002-99597115	XLOC_006188
6	lnc-ZKSCAN1-1	chr7:99605669-99605945	XLOC_006188
7	lnc-ZKSCAN1-1	chr7:99608999-99609247	XLOC_006188
8	lnc-ZKSCAN1-1	chr7:99595355-99595546	XLOC_006188
9	lnc-ZKSCAN1-1	chr7:99594667-99594733	XLOC_006188
10	lnc-ZKSCAN1-1	chr7:99608999-99609249	XLOC_006188
11	lnc-ZKSCAN1-2	chr7:99587971-99588326	expReg_chr7_6373_+
12	lnc-ZKSCAN1-1	chr7:99605931-99605945	XLOC_006188
13	lnc-ZKSCAN1-1	chr7:99597006-99597115	XLOC_006188
14	lnc-ZKSCAN1-1	chr7:99608999-99609239	XLOC_006188

No data

Variant related genes	Relation type
ZKSCAN1	TF binding region
ENSG00000235713	TF binding region
AZGP1	TF binding region
AZGP1P1	TF binding region
ZKSCAN1	CpG island
ENSG00000235713	CpG island
AZGP1	CpG island
AZGP1P1	CpG island
ENSG00000051108	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000272888	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000106261	chromatin interactions
ENSG00000235077	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000242798	chromatin interactions
ENSG00000166997	chromatin interactions
ENSG00000197037	chromatin interactions
ENSG00000214309	chromatin interactions
ENSG00000146826	chromatin interactions
ENSG00000137154	chromatin interactions
ENSG00000176402	chromatin interactions
ENSG00000214252	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000168090	chromatin interactions
ENSG00000146833	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000160862	chromatin interactions
ENSG00000235713	chromatin interactions
ENSG00000237640	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000166529	chromatin interactions
ENSG00000166526	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000106290	chromatin interactions
BRD1	miRNA target sites
KCTD15	miRNA target sites
C11orf82	miRNA target sites
NUP153	miRNA target sites
TMEM45A	miRNA target sites
ARSJ	miRNA target sites
ASCC2	miRNA target sites

Extended variants
information (count: 2714 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2714 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186499068	chr7:99566312-99566313	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs535686357	chr7:99566323-99566324	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs557289720	chr7:99566336-99566337	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs71569525	chr7:99566387-99566388	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs575563119	chr7:99566406-99566407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs2525554	chr7:99566407-99566408	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs34349564	chr7:99566415-99566416	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs35479339	chr7:99566418-99566419	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs189702440	chr7:99566442-99566443	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs572771918	chr7:99566486-99566487	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376385268	chr7:99566500-99566501	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371111343	chr7:99566563-99566564	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560191375	chr7:99566568-99566569	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs71569526	chr7:99566583-99566584	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs71515293	chr7:99566624-99566625	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540301904	chr7:99566677-99566678	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527751011	chr7:99566678-99566679	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs147378786	chr7:99566695-99566696	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544452987	chr7:99566725-99566726	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs182414106	chr7:99566757-99566758	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs566775570	chr7:99566758-99566759	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs533408907	chr7:99566761-99566762	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs552267700	chr7:99566777-99566778	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs545396111	chr7:99566779-99566780	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs374184755	chr7:99566798-99566799	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564208514	chr7:99566801-99566802	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs137980992	chr7:99566810-99566811	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs564480036	chr7:99566855-99566856	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531933118	chr7:99566930-99566931	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549446038	chr7:99566939-99566940	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs567804996	chr7:99566946-99566947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs534232037	chr7:99566947-99566948	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs543684094	chr7:99566954-99566955	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs531845520	chr7:99566980-99566981	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550206577	chr7:99566989-99566990	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs34635346	chr7:99567031-99567032	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs3033213	chr7:99567047-99567048	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550754219	chr7:99567138-99567139	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs569088449	chr7:99567158-99567159	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs2527924	chr7:99567195-99567196	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs34935399	chr7:99567203-99567204	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs149513858	chr7:99567271-99567272	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs79039815	chr7:99567380-99567381	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563904304	chr7:99567396-99567397	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187075417	chr7:99567416-99567417	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs2527923	chr7:99567455-99567456	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs191594465	chr7:99567469-99567470	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573356459	chr7:99567471-99567472	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183049437	chr7:99567473-99567474	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs556307734	chr7:99567478-99567479	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
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
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2412 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99562600-99573000	Weak transcription	Left Ventricle	heart
2	chr7:99563200-99567000	Strong transcription	Liver	Liver
3	chr7:99563400-99572800	Weak transcription	Brain Substantia Nigra	brain
4	chr7:99563400-99573000	Weak transcription	Gastric	stomach
5	chr7:99564800-99567600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:99565400-99571600	Weak transcription	Adipose Nuclei	Adipose
7	chr7:99565600-99567600	Weak transcription	Pancreas	Pancrea
8	chr7:99565800-99568200	Weak transcription	HepG2	liver
9	chr7:99566000-99572400	Weak transcription	Right Ventricle	heart
10	chr7:99566800-99567000	Enhancers	Lung	lung
11	chr7:99567000-99569000	Weak transcription	Lung	lung
12	chr7:99567000-99570600	Genic enhancers	Liver	Liver
13	chr7:99567600-99567800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:99567600-99567800	Enhancers	Pancreas	Pancrea
15	chr7:99567800-99568200	Weak transcription	Pancreas	Pancrea
16	chr7:99567800-99578000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:99568200-99569600	Strong transcription	HepG2	liver
18	chr7:99568200-99570000	Genic enhancers	Pancreas	Pancrea
19	chr7:99568400-99568800	Weak transcription	Brain Anterior Caudate	brain
20	chr7:99569000-99569600	Enhancers	Lung	lung
21	chr7:99569600-99571600	Weak transcription	HepG2	liver
22	chr7:99570000-99570400	Enhancers	Pancreas	Pancrea
23	chr7:99570400-99572600	Weak transcription	Pancreas	Pancrea
24	chr7:99570600-99570800	Enhancers	Liver	Liver
25	chr7:99570800-99571400	Flanking Active TSS	Liver	Liver
26	chr7:99571400-99573800	Active TSS	Liver	Liver
27	chr7:99571600-99571800	Enhancers	Adipose Nuclei	Adipose
28	chr7:99571600-99572400	Enhancers	HepG2	liver
29	chr7:99571800-99572400	Weak transcription	Adipose Nuclei	Adipose
30	chr7:99572400-99572600	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr7:99572400-99572800	Flanking Active TSS	HepG2	liver
32	chr7:99572400-99573600	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr7:99572400-99573600	Active TSS	Right Ventricle	heart
34	chr7:99572600-99573400	Active TSS	Adipose Nuclei	Adipose
35	chr7:99572600-99573800	Active TSS	Pancreas	Pancrea
36	chr7:99572800-99573800	Active TSS	HepG2	liver
37	chr7:99572800-99574000	Active TSS	Brain Substantia Nigra	brain
38	chr7:99572800-99574200	Enhancers	Brain Cingulate Gyrus	brain
39	chr7:99573000-99573600	Active TSS	Duodenum Mucosa	Duodenum
40	chr7:99573000-99573600	Active TSS	Left Ventricle	heart
41	chr7:99573000-99573800	Active TSS	Gastric	stomach
42	chr7:99573000-99574200	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr7:99573400-99573800	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr7:99573400-99573800	Active TSS	Brain Anterior Caudate	brain
45	chr7:99573400-99574200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:99573400-99574400	Enhancers	Fetal Intestine Small	intestine
47	chr7:99573400-99574600	Enhancers	Stomach Mucosa	stomach
48	chr7:99573600-99573800	Enhancers	Brain Hippocampus Middle	brain
49	chr7:99573600-99573800	Weak transcription	Duodenum Mucosa	Duodenum
50	chr7:99573600-99573800	Enhancers	Left Ventricle	heart

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