Variant report

Variant	esv1818748
Chromosome Location	chr7:123829886-124039708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:673)
CpG islands
(count:305)
Chromatin interactive
region (count:25)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:123953326-123953442	K562	blood:	n/a	n/a
2	ATF1	chr7:123909888-123910120	K562	blood:	n/a	n/a
3	ATF1	chr7:123886598-123886729	K562	blood:	n/a	n/a
4	ATF1	chr7:123903518-123903832	K562	blood:	n/a	n/a
5	ATF1	chr7:124026607-124026805	K562	blood:	n/a	n/a
6	ATF1	chr7:123950919-123951365	K562	blood:	n/a	n/a
7	ATF2	chr7:123903345-123903808	GM12878	blood:	n/a	n/a
8	ATF2	chr7:123897573-123898594	GM12878	blood:	n/a	n/a
9	ATF3	chr7:123903568-123903806	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:123903479-123903869	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr7:123903532-123903773	GM12878	blood:	n/a	n/a
12	BACH1	chr7:124009494-124009604	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:123885688-123885883	GM12878	blood:	n/a	chr7:123885771-123885782
14	BATF	chr7:123897707-123898119	GM12878	blood:	n/a	chr7:123897898-123897908 chr7:123897902-123897912 chr7:123897901-123897912
15	BATF	chr7:123885644-123885946	GM12878	blood:	n/a	chr7:123885771-123885782
16	BATF	chr7:123903526-123903804	GM12878	blood:	n/a	n/a
17	BATF	chr7:123903522-123903804	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:123885636-123885907	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:123897642-123898236	GM12878	blood:	n/a	chr7:123898197-123898206 chr7:123897901-123897910
20	BHLHE40	chr7:123885646-123885828	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:123903573-123903692	GM12878	blood:	n/a	n/a
22	BRCA1	chr7:123915746-123915818	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr7:123849911-123849930	Hela-S3	cervix:	n/a	n/a
24	CCNT2	chr7:124019650-124019721	K562	blood:	n/a	n/a
25	CEBPB	chr7:123903383-123903885	HCT-116	colon:	n/a	chr7:123903693-123903704
26	CEBPB	chr7:123884916-123885153	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:124013892-124014116	K562	blood:	n/a	n/a
28	CEBPB	chr7:123950885-123951358	HCT-116	colon:	n/a	n/a
29	CEBPB	chr7:124027875-124028066	HepG2	liver:	n/a	chr7:124027967-124027978
30	CEBPB	chr7:123866027-123866202	A549	lung:	n/a	chr7:123866140-123866157 chr7:123866141-123866152 chr7:123866142-123866153 chr7:123866141-123866154 chr7:123866141-123866152 chr7:123866141-123866154 chr7:123866141-123866154
31	CEBPB	chr7:123882670-123882986	IMR90	lung:	n/a	chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882822 chr7:123882809-123882822 chr7:123882809-123882822 chr7:123882811-123882820 chr7:123882809-123882820
32	CEBPB	chr7:123950894-123951209	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:123882776-123882944	K562	blood:	n/a	chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882822 chr7:123882809-123882822 chr7:123882809-123882822 chr7:123882811-123882820 chr7:123882809-123882820
34	CEBPB	chr7:124009369-124009705	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:123903360-123903944	H1-hESC	embryonic stem cell:	n/a	chr7:123903693-123903704
36	CEBPB	chr7:124013825-124014114	A549	lung:	n/a	n/a
37	CEBPB	chr7:124013810-124014125	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr7:124035161-124035500	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:123915528-123915868	H1-hESC	embryonic stem cell:	n/a	chr7:123915698-123915709 chr7:123915698-123915711
40	CEBPB	chr7:123838141-123838287	HepG2	liver:	n/a	chr7:123838217-123838228
41	CEBPB	chr7:123903391-123903997	GM12878	blood:	n/a	chr7:123903693-123903704
42	CEBPB	chr7:123977376-123977659	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:123879945-123880044	HepG2	liver:	n/a	chr7:123879983-123879994
44	CEBPB	chr7:124035162-124035516	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:123903529-123903831	A549	lung:	n/a	chr7:123903693-123903704
46	CEBPB	chr7:124035204-124035481	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:124035154-124035475	A549	lung:	n/a	n/a
48	CEBPB	chr7:123903512-123903887	Hela-S3	cervix:	n/a	chr7:123903693-123903704
49	CEBPB	chr7:123903472-123904002	HCT-116	colon:	n/a	chr7:123903693-123903704
50	CEBPB	chr7:123882722-123882910	A549	lung:	n/a	chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882822 chr7:123882809-123882822 chr7:123882809-123882822 chr7:123882811-123882820 chr7:123882809-123882820

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:123978181-123978231	AG04449	skin:	fetal
2	chr7:123992223-123992273	MCF-7	breast:	n/a
3	chr7:123978181-123978231	PrEC	prostate:	n/a
4	chr7:123903317-123903367	NHBE	bronchial:	n/a
5	chr7:123992223-123992273	HCM	heart:	n/a
6	chr7:123992223-123992273	HUVEC	blood vessel:	n/a
7	chr7:123903317-123903367	SK-N-SH	brain:	n/a
8	chr7:123916407-123916457	PFSK-1	brain:	n/a
9	chr7:123916407-123916457	K562	blood:	n/a
10	chr7:123842309-123842359	AG09319	gingival:	n/a
11	chr7:123978181-123978231	HCPEpiC	choroid plexus:	n/a
12	chr7:123992223-123992273	HRE	kidney:	n/a
13	chr7:123992223-123992273	Caco-2	colon:	n/a
14	chr7:123992223-123992273	Jurkat	blood:	n/a
15	chr7:123916407-123916457	HL-60	blood:	n/a
16	chr7:123842309-123842359	NH-A	brain:	n/a
17	chr7:123978181-123978231	HMEC	breast:	n/a
18	chr7:123992223-123992273	HCPEpiC	choroid plexus:	n/a
19	chr7:123978181-123978231	SK-N-SH	brain:	n/a
20	chr7:123842309-123842359	HRE	kidney:	n/a
21	chr7:123903317-123903367	HCT-116	colon:	n/a
22	chr7:123916407-123916457	U87	brain:	n/a
23	chr7:123916407-123916457	NH-A	brain:	n/a
24	chr7:123992223-123992273	HRCEpiC	kidney:	n/a
25	chr7:123978181-123978231	NH-A	brain:	n/a
26	chr7:123903317-123903367	K562	blood:	n/a
27	chr7:123842309-123842359	HRPEpiC	eye:	n/a
28	chr7:123978181-123978231	HEK293	kidney:	embryo
29	chr7:123992223-123992273	PrEC	prostate:	n/a
30	chr7:123842309-123842359	RPTEC	kidney:	n/a
31	chr7:123842309-123842359	HEEpiC	esophagus:	n/a
32	chr7:123842309-123842359	PrEC	prostate:	n/a
33	chr7:123903317-123903367	AoSMC	blood vessel:	n/a
34	chr7:123903317-123903367	U87	brain:	n/a
35	chr7:123992223-123992273	NH-A	brain:	n/a
36	chr7:123978181-123978231	ECC-1	luminal epithelium:	n/a
37	chr7:123903317-123903367	HRPEpiC	eye:	n/a
38	chr7:123916407-123916457	PrEC	prostate:	n/a
39	chr7:123903317-123903367	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:123842309-123842359	NHDF-neo	bronchial:	n/a
41	chr7:123903317-123903367	PANC-1	pancreas:	n/a
42	chr7:123992223-123992273	HepG2	liver:	n/a
43	chr7:123903317-123903367	CMK	blood:	n/a
44	chr7:123916407-123916457	Caco-2	colon:	n/a
45	chr7:123992223-123992273	BE2_C	brain:	n/a
46	chr7:123916407-123916457	Jurkat	blood:	n/a
47	chr7:123916407-123916457	IMR90	lung:	fetal
48	chr7:123916407-123916457	GM12878	blood:	n/a
49	chr7:123978181-123978231	SKMC	muscle:	n/a
50	chr7:123903317-123903367	HEK293	kidney:	embryo

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:123854533..123856371-chr7:123856582..123859450,2	K562	blood:
2	chr7:123973378..123975261-chr7:123975911..123978785,2	K562	blood:
3	chr7:123831215..123834042-chr7:123835475..123837132,2	K562	blood:
4	chr7:123887405..123889302-chr7:123890495..123893294,2	K562	blood:
5	chr7:123938093..123940517-chr7:124074999..124077404,2	K562	blood:
6	chr3:64234460..64234993-chr7:123973379..123973879,2	MCF-7	breast:
7	chr7:123858356..123860214-chr7:123862042..123864600,2	K562	blood:
8	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
9	chr7:123828369..123831335-chr7:123834252..123836029,2	MCF-7	breast:
10	chr7:123915423..123917674-chr7:123921407..123924592,3	K562	blood:
11	chr7:123892945..123894583-chr7:123896590..123898487,2	K562	blood:
12	chr20:52367901..52368731-chr7:123854009..123854727,2	MCF-7	breast:
13	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
14	chr7:123828369..123831335-chr7:123834252..123836029,2	MCF-7	breast:
15	chr7:123840358..123843025-chr7:123844759..123847576,2	K562	blood:
16	chr7:123858356..123860214-chr7:123862042..123864600,2	K562	blood:
17	chr7:123996206..123998785-chr8:77412686..77415296,2	MCF-7	breast:
18	chr7:123840358..123843025-chr7:123844759..123847576,2	K562	blood:
19	chr7:124018038..124020966-chr7:124025116..124027291,2	MCF-7	breast:
20	chr7:123831215..123834042-chr7:123835475..123837132,2	K562	blood:
21	chr7:123915423..123917674-chr7:123921407..123924592,3	K562	blood:
22	chr7:123887405..123889302-chr7:123890495..123893294,2	K562	blood:
23	chr7:123892945..123894583-chr7:123896590..123898487,2	K562	blood:
24	chr7:123854533..123856371-chr7:123856582..123859450,2	K562	blood:
25	chr7:124018038..124020966-chr7:124025116..124027291,2	MCF-7	breast:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
2	lnc-SPAM1-3	chr7:123993205-123993469	XLOC_006228
3	lnc-TMEM229A-1	chr7:123914775-123915052	NONHSAT123078
4	lnc-TMEM229A-1	chr7:123927269-123927598	XLOC_006590
5	lnc-SPAM1-3	chr7:124000163-124000252	ENSG00000242593.1
6	lnc-TMEM229A-1	chr7:123928853-123928911	NONHSAT123077
7	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
8	lnc-SPAM1-3	chr7:124031483-124035172	ENSG00000242593.1
9	lnc-SPAM1-3	chr7:123992870-123992905	XLOC_006228
10	lnc-SPAM1-3	chr7:124028495-124028581	NONHSAT123082
11	lnc-SPAM1-3	chr7:124027821-124028581	XLOC_006229
12	lnc-SPAM1-3	chr7:124032563-124032795	NONHSAT123082
13	lnc-TMEM229A-1	chr7:123927269-123927344	NONHSAT123078
14	lnc-SPAM1-3	chr7:124029526-124029556	XLOC_006229
15	lnc-TMEM229A-2	chr7:123989883-123989978	XLOC_006591
16	lnc-TMEM229A-2	chr7:123977434-123977554	NR_110180
17	lnc-TMEM229A-1	chr7:123914733-123915052	XLOC_006590
18	lnc-TMEM229A-2	chr7:123989883-123989978	NR_110180
19	lnc-TMEM229A-2	chr7:123982515-123982615	NR_110180
20	lnc-TMEM229A-2	chr7:123989883-123989914	XLOC_006591
21	lnc-TMEM229A-1	chr7:123928853-123928879	NONHSAT123078
22	lnc-SPAM1-3	chr7:124016376-124016450	ENSG00000242593.1
23	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
24	lnc-TMEM229A-2	chr7:123991905-123992154	XLOC_006591
25	lnc-SPAM1-3	chr7:124025652-124025703	ENSG00000242593.1
26	lnc-TMEM229A-2	chr7:123991905-123992150	NR_110180
27	lnc-SPAM1-3	chr7:124029526-124029610	ENSG00000242593.1
28	lnc-SPAM1-3	chr7:124028468-124028581	ENSG00000242593.1
29	lnc-SPAM1-3	chr7:123974348-123974485	XLOC_006228
30	lnc-SPAM1-3	chr7:123992870-123992905	ENSG00000242593.1
31	lnc-TMEM229A-1	chr7:123914775-123915052	NONHSAT123077
32	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
33	lnc-SPAM1-3	chr7:124029526-124029610	NONHSAT123082

No data

Variant related genes	Relation type
ENSG00000242593	TF binding region
ENSG00000243574	TF binding region
ENSG00000241324	TF binding region
ENSG00000242593	CpG island
ENSG00000243574	CpG island
ENSG00000241324	CpG island
ENSG00000242593	chromatin interactions
C6orf168	miRNA target sites

Extended variants
information (count: 3956 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3956 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552006178	chr7:123829895-123829896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577808803	chr7:123829922-123829923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545077519	chr7:123829960-123829961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140867144	chr7:123830002-123830003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35247451	chr7:123830043-123830044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541319485	chr7:123830048-123830049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7801264	chr7:123830069-123830070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77753394	chr7:123830125-123830126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7801144	chr7:123830138-123830139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573025250	chr7:123830171-123830172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538464449	chr7:123830216-123830217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7801530	chr7:123830218-123830219	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs575495867	chr7:123830229-123830230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370977445	chr7:123830239-123830240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544173008	chr7:123830264-123830265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560585255	chr7:123830271-123830272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574110543	chr7:123830275-123830276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75196715	chr7:123830279-123830280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559820902	chr7:123830280-123830281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560944524	chr7:123830297-123830298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528647598	chr7:123830306-123830307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531408562	chr7:123830307-123830308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146194351	chr7:123830332-123830333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572275274	chr7:123830375-123830376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71531955	chr7:123830399-123830400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531141000	chr7:123830407-123830408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573821436	chr7:123830421-123830422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200199507	chr7:123830508-123830509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542466468	chr7:123830565-123830566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141939090	chr7:123830569-123830570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551268514	chr7:123830582-123830583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567634948	chr7:123830633-123830634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7805323	chr7:123830652-123830653	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs567009784	chr7:123830653-123830654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147813234	chr7:123830668-123830669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558498040	chr7:123830673-123830674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560298458	chr7:123830697-123830698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191034209	chr7:123830717-123830718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372792511	chr7:123830727-123830728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564821554	chr7:123830729-123830730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7805343	chr7:123830730-123830731	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550930944	chr7:123830770-123830771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183345180	chr7:123830787-123830788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77144562	chr7:123830813-123830814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553443972	chr7:123830923-123830924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576914515	chr7:123830968-123830969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545564888	chr7:123830969-123830970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141383254	chr7:123831040-123831041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs118059869	chr7:123831048-123831049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544871128	chr7:123831067-123831068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	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
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:123828000-123832400	Enhancers	Fetal Heart	heart
2	chr7:123828200-123832000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:123828600-123830800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:123829200-123831000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:123829400-123831000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr7:123829600-123830800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:123829800-123830800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:123829800-123831000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:123830000-123830200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:123830200-123831000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:123830800-123831400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:123830800-123831600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:123830800-123831600	Enhancers	Brain Cingulate Gyrus	brain
14	chr7:123830800-123842200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:123831000-123831200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:123831000-123831200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr7:123831000-123831400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:123831000-123831600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:123831000-123831600	Enhancers	Brain Hippocampus Middle	brain
20	chr7:123831000-123831600	Enhancers	Brain Substantia Nigra	brain
21	chr7:123831000-123832000	Enhancers	Brain Anterior Caudate	brain
22	chr7:123831200-123831400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr7:123831200-123831800	Enhancers	Fetal Lung	lung
24	chr7:123831800-123836600	Weak transcription	Fetal Lung	lung
25	chr7:123833400-123834400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:123836600-123836800	Enhancers	Fetal Lung	lung
27	chr7:123836800-123837200	Weak transcription	Fetal Lung	lung
28	chr7:123837200-123837600	Enhancers	Fetal Lung	lung
29	chr7:123841600-123842400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:123841600-123843000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr7:123841800-123842200	Enhancers	Hela-S3	cervix
32	chr7:123841800-123842600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:123841800-123842600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:123841800-123842600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:123842200-123843000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:123842600-123845600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:123843000-123843600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:123843600-123843800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:123843800-123845600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:123845400-123846000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:123845600-123845800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:123845600-123846000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:123846000-123848400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:123847800-123849200	Enhancers	Fetal Brain Male	brain
45	chr7:123848400-123849000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:123850200-123850400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:123857800-123858400	Enhancers	Adipose Nuclei	Adipose
48	chr7:123859600-123861600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:123861400-123862000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr7:123861600-123862000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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