Variant report

Variant	esv3371602
Chromosome Location	chr15:83476798-83481096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:771)
CpG islands
(count:855)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:83479918-83480157	K562	blood:	n/a	n/a
2	ARID3A	chr15:83478011-83478623	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:83477457-83477462	HepG2	liver:	n/a	n/a
4	ATF1	chr15:83478096-83478472	K562	blood:	n/a	n/a
5	ATF2	chr15:83479287-83480364	GM12878	blood:	n/a	n/a
6	ATF2	chr15:83479355-83480327	GM12878	blood:	n/a	n/a
7	BACH1	chr15:83478703-83479200	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr15:83479819-83480227	GM12878	blood:	n/a	n/a
9	BATF	chr15:83479342-83480289	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:83479559-83480160	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:83479278-83480283	GM12878	blood:	n/a	n/a
12	BCL3	chr15:83479847-83480193	GM12878	blood:	n/a	n/a
13	BCL3	chr15:83478090-83478684	A549	lung:	n/a	chr15:83478308-83478321
14	BCLAF1	chr15:83478253-83478873	GM12878	blood:	n/a	chr15:83478308-83478321
15	BCLAF1	chr15:83479251-83480322	GM12878	blood:	n/a	n/a
16	BCLAF1	chr15:83479577-83480105	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:83477990-83478738	HepG2	liver:	n/a	n/a
18	BHLHE40	chr15:83478064-83479667	K562	blood:	n/a	chr15:83479238-83479254
19	BHLHE40	chr15:83479558-83480312	GM12878	blood:	n/a	n/a
20	BHLHE40	chr15:83477856-83479095	GM12878	blood:	n/a	n/a
21	BRCA1	chr15:83479069-83479078	HepG2	liver:	n/a	n/a
22	BRCA1	chr15:83479019-83479131	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr15:83478091-83478611	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr15:83477918-83478761	K562	blood:	n/a	n/a
25	CCNT2	chr15:83478142-83479327	K562	blood:	n/a	n/a
26	CEBPB	chr15:83477972-83478425	K562	blood:	n/a	chr15:83478322-83478330
27	CEBPB	chr15:83478002-83478537	HepG2	liver:	n/a	chr15:83478322-83478330
28	CEBPB	chr15:83477946-83478388	A549	lung:	n/a	chr15:83478322-83478330
29	CEBPB	chr15:83479061-83479583	A549	lung:	n/a	n/a
30	CEBPB	chr15:83477994-83478399	IMR90	lung:	n/a	chr15:83478322-83478330
31	CEBPB	chr15:83477980-83478392	ECC-1	luminal epithelium:	n/a	chr15:83478322-83478330
32	CEBPB	chr15:83479212-83479564	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:83479279-83479515	K562	blood:	n/a	n/a
34	CEBPB	chr15:83477904-83478473	MCF-7	breast:	n/a	chr15:83478322-83478330
35	CEBPB	chr15:83477981-83478530	HepG2	liver:	n/a	chr15:83478322-83478330
36	CEBPB	chr15:83478049-83478219	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:83477906-83478369	K562	blood:	n/a	chr15:83478322-83478330
38	CEBPB	chr15:83478053-83478300	HepG2	liver:	n/a	n/a
39	CEBPB	chr15:83477967-83478790	Hela-S3	cervix:	n/a	chr15:83478322-83478330
40	CEBPB	chr15:83477974-83478432	ECC-1	luminal epithelium:	n/a	chr15:83478322-83478330
41	CEBPB	chr15:83479281-83479434	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr15:83478923-83479525	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:83479189-83480121	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr15:83479364-83480383	GM12878	blood:	n/a	n/a
45	CEBPB	chr15:83478031-83478356	A549	lung:	n/a	chr15:83478322-83478330
46	CEBPB	chr15:83479983-83480095	K562	blood:	n/a	n/a
47	CEBPB	chr15:83477978-83478361	H1-hESC	embryonic stem cell:	n/a	chr15:83478322-83478330
48	CEBPB	chr15:83477978-83478306	K562	blood:	n/a	n/a
49	CEBPB	chr15:83477853-83478531	A549	lung:	n/a	chr15:83478322-83478330
50	CEBPB	chr15:83477902-83478435	MCF-7	breast:	n/a	chr15:83478322-83478330

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:83479213-83479263	AG09319	gingival:	n/a
2	chr15:83479213-83479263	AG09319	gingival:	n/a
3	chr15:83479272-83479322	AG10803	skin:	n/a
4	chr15:83478541-83478591	HCF	heart:	n/a
5	chr15:83477915-83477965	Hela-S3	cervix:	n/a
6	chr15:83478878-83478928	HRPEpiC	eye:	n/a
7	chr15:83477712-83477762	HepG2	liver:	n/a
8	chr15:83478411-83478461	HRPEpiC	eye:	n/a
9	chr15:83478367-83478417	GM12891	blood:	n/a
10	chr15:83478255-83478305	SKMC	muscle:	n/a
11	chr15:83478541-83478591	HRCEpiC	kidney:	n/a
12	chr15:83480317-83480367	HAEpiC	amniotic membrane:	n/a
13	chr15:83477915-83477965	SAEC	small airway:	n/a
14	chr15:83477712-83477762	HRCEpiC	kidney:	n/a
15	chr15:83479213-83479263	HPAEpiC	pulmonary alveolar:	n/a
16	chr15:83478878-83478928	AG04450	lung:	fetal
17	chr15:83477872-83477922	HIPEpiC	eye:	n/a
18	chr15:83479272-83479322	H1-hESC	embryonic stem cell:	embryo
19	chr15:83477965-83478015	RPTEC	kidney:	n/a
20	chr15:83478411-83478461	AG09309	skin:	n/a
21	chr15:83477915-83477965	GM12878	blood:	n/a
22	chr15:83478255-83478305	H1-hESC	embryonic stem cell:	embryo
23	chr15:83478411-83478461	BJ	skin:	n/a
24	chr15:83477872-83477922	HPAEpiC	pulmonary alveolar:	n/a
25	chr15:83480317-83480367	SK-N-SH_RA	brain:	n/a
26	chr15:83478524-83478574	GM12892	blood:	n/a
27	chr15:83480317-83480367	BE2_C	brain:	n/a
28	chr15:83478541-83478591	AoSMC	blood vessel:	n/a
29	chr15:83479272-83479322	PFSK-1	brain:	n/a
30	chr15:83477608-83477658	HL-60	blood:	n/a
31	chr15:83478411-83478461	GM12891	blood:	n/a
32	chr15:83479213-83479263	CMK	blood:	n/a
33	chr15:83478411-83478461	HMEC	breast:	n/a
34	chr15:83477608-83477658	GM12892	blood:	n/a
35	chr15:83478255-83478305	RPTEC	kidney:	n/a
36	chr15:83478411-83478461	HAEpiC	amniotic membrane:	n/a
37	chr15:83480317-83480367	CMK	blood:	n/a
38	chr15:83477712-83477762	HCPEpiC	choroid plexus:	n/a
39	chr15:83478541-83478591	RPTEC	kidney:	n/a
40	chr15:83477712-83477762	ECC-1	luminal epithelium:	n/a
41	chr15:83480317-83480367	SAEC	small airway:	n/a
42	chr15:83477608-83477658	CMK	blood:	n/a
43	chr15:83479213-83479263	NH-A	brain:	n/a
44	chr15:83480317-83480367	HEEpiC	esophagus:	n/a
45	chr15:83478524-83478574	AG09319	gingival:	n/a
46	chr15:83477965-83478015	HCT-116	colon:	n/a
47	chr15:83477712-83477762	NHDF-neo	bronchial:	n/a
48	chr15:83478367-83478417	RPTEC	kidney:	n/a
49	chr15:83478255-83478305	HMEC	breast:	n/a
50	chr15:83479272-83479322	PrEC	prostate:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:83346623..83348757-chr15:83479507..83481301,2	K562	blood:
2	chr15:83417832..83422548-chr15:83476028..83480956,9	K562	blood:
3	chr15:83478686..83480372-chr15:83679248..83681221,2	MCF-7	breast:
4	chr15:83477554..83479674-chr15:83486165..83489315,3	MCF-7	breast:
5	chr15:83417500..83421911-chr15:83474614..83480217,8	MCF-7	breast:
6	chr15:83417361..83424147-chr15:83476165..83481050,26	MCF-7	breast:
7	chr15:83478234..83479933-chr15:83485060..83487669,2	K562	blood:
8	chr15:83478198..83478889-chr5:102455539..102456094,2	Hela-S3	cervix:
9	chr15:83478347..83478879-chr2:10182698..10183566,2	Hela-S3	cervix:
10	chr15:83333197..83334998-chr15:83479229..83480988,2	MCF-7	breast:
11	chr15:83438498..83441390-chr15:83475483..83477867,2	K562	blood:
12	chr15:83313427..83317808-chr15:83477553..83483000,6	K562	blood:
13	chr15:83478077..83478694-chr19:56632004..56632840,2	Hela-S3	cervix:
14	chr15:83376836..83378789-chr15:83478421..83480593,2	MCF-7	breast:
15	chr15:83480184..83483063-chr15:83673551..83675141,2	K562	blood:
16	chr15:83407361..83409606-chr15:83477408..83479472,2	MCF-7	breast:
17	chr15:83476033..83478214-chr15:83679893..83681510,2	K562	blood:
18	chr15:83478211..83480402-chr15:83735487..83737469,2	MCF-7	breast:
19	chr15:83477632..83480172-chr15:83484528..83487051,2	MCF-7	breast:
20	chr15:83478452..83480034-chr15:83499455..83501748,2	MCF-7	breast:
21	chr15:83347885..83349520-chr15:83478710..83480628,2	MCF-7	breast:
22	chr15:83477529..83479377-chr15:83517237..83520056,3	K562	blood:
23	chr15:83478559..83480416-chr15:83489248..83490840,2	MCF-7	breast:
24	chr15:83475882..83480852-chr15:83678880..83683242,6	MCF-7	breast:
25	chr15:83477527..83479377-chr15:83517237..83519936,2	K562	blood:
26	chr1:153508043..153508984-chr15:83478155..83479111,2	Hela-S3	cervix:
27	chr15:83478349..83478996-chr5:98264221..98265198,2	Hela-S3	cervix:
28	chr15:83478011..83478847-chr17:26988790..26989739,2	Hela-S3	cervix:
29	chr15:83479049..83481749-chr15:83503841..83505564,2	K562	blood:
30	chr15:83478214..83478879-chr6:24720555..24721193,2	Hela-S3	cervix:
31	chr15:83417749..83420684-chr15:83476028..83479878,6	K562	blood:
32	chr15:83477828..83481866-chr15:83483118..83489176,7	K562	blood:
33	chr15:83348193..83350766-chr15:83477443..83480779,4	MCF-7	breast:
34	chr15:83476157..83479071-chr15:83480775..83482878,2	K562	blood:
35	chr15:83396804..83398373-chr15:83475659..83477740,2	MCF-7	breast:
36	chr15:83423255..83426158-chr15:83477607..83479598,3	MCF-7	breast:
37	chr15:83476923..83480237-chr15:83875108..83878990,4	MCF-7	breast:
38	chr15:83418742..83419414-chr15:83478376..83479191,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
WHAMM	TF binding region
FSD2	TF binding region
WHAMM	CpG island
FSD2	CpG island
ENSG00000169609	chromatin interactions
ENSG00000166503	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000156232	chromatin interactions
ENSG00000145723	chromatin interactions
ENSG00000172059	chromatin interactions
ENSG00000259315	chromatin interactions
ENSG00000132581	chromatin interactions
ENSG00000214575	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000260608	chromatin interactions
ENSG00000064726	chromatin interactions
ENSG00000103723	chromatin interactions
ENSG00000142409	chromatin interactions
ENSG00000145725	chromatin interactions
ENSG00000248489	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000263643	chromatin interactions
ENSG00000103942	chromatin interactions
ENSG00000259462	chromatin interactions
ENSG00000250988	chromatin interactions
ENSG00000252690	chromatin interactions

Extended variants
information (count: 135 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:135 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191374148	chr15:83476825-83476826	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs146542734	chr15:83476840-83476841	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs546816894	chr15:83476852-83476853	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs571767181	chr15:83476969-83476970	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs182708770	chr15:83477029-83477030	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs117771133	chr15:83477075-83477076	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs114861351	chr15:83477080-83477081	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs549330976	chr15:83477094-83477095	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs569424975	chr15:83477126-83477127	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs532053134	chr15:83477128-83477129	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs552142258	chr15:83477136-83477137	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs77517139	chr15:83477145-83477146	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs533579563	chr15:83477183-83477184	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs553714830	chr15:83477210-83477211	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs140196357	chr15:83477267-83477268	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs187033457	chr15:83477298-83477299	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs557374847	chr15:83477308-83477309	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs369224022	chr15:83477371-83477372	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs77751505	chr15:83477441-83477442	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs375148812	chr15:83477544-83477545	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs556090721	chr15:83477547-83477548	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs575794695	chr15:83477551-83477552	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs544796540	chr15:83477595-83477596	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
24	rs558472207	chr15:83477597-83477598	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
25	rs72753974	chr15:83477614-83477615	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145849324	chr15:83477645-83477646	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs560507719	chr15:83477653-83477654	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs148984026	chr15:83477677-83477678	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs564978129	chr15:83477700-83477701	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs191924734	chr15:83477705-83477706	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs145211401	chr15:83477706-83477707	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
32	rs562961341	chr15:83477707-83477708	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
33	rs182943078	chr15:83477713-83477714	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
34	rs373250221	chr15:83477733-83477734	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
35	rs537086155	chr15:83477742-83477743	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
36	rs188946231	chr15:83477787-83477788	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
37	rs193128920	chr15:83477804-83477805	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
38	rs143739490	chr15:83477825-83477826	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
39	rs371528838	chr15:83477881-83477882	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs184406339	chr15:83477889-83477890	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
41	rs376761034	chr15:83477933-83477934	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
42	rs187769789	chr15:83477966-83477967	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
43	rs569411216	chr15:83477984-83477985	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
44	rs538475965	chr15:83478012-83478013	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs558293747	chr15:83478051-83478052	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs572029038	chr15:83478070-83478071	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs199846096	chr15:83478154-83478155	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
48	rs8042254	chr15:83478169-83478170	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs150969408	chr15:83478172-83478173	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
50	rs563480880	chr15:83478196-83478197	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
abnormal development	18461090	CNVD
Intellectual disability	22102821	CNVD
renal disease	17924346	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:83450400-83477600	Weak transcription	Brain Hippocampus Middle	brain
2	chr15:83469200-83477600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr15:83469400-83477600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr15:83469800-83477400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr15:83471000-83477600	Weak transcription	Spleen	Spleen
6	chr15:83471200-83478200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr15:83472000-83477800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr15:83472400-83478200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:83473600-83477600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr15:83473600-83477800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr15:83473800-83477400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:83473800-83477600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr15:83473800-83477600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:83473800-83477600	Weak transcription	NHEK	skin
15	chr15:83474000-83477400	Weak transcription	HMEC	breast
16	chr15:83474800-83477400	Weak transcription	Right Ventricle	heart
17	chr15:83474800-83477600	Weak transcription	Brain Angular Gyrus	brain
18	chr15:83475000-83477400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr15:83475000-83477400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr15:83475000-83477400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr15:83475000-83477400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr15:83475000-83477400	Weak transcription	Pancreas	Pancrea
23	chr15:83475000-83478400	Weak transcription	Left Ventricle	heart
24	chr15:83475200-83477200	Weak transcription	K562	blood
25	chr15:83475200-83477400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr15:83475200-83477400	Weak transcription	HSMM	muscle
27	chr15:83475200-83477400	Weak transcription	HSMMtube	muscle
28	chr15:83475400-83477200	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr15:83475400-83477200	Weak transcription	Hela-S3	cervix
30	chr15:83475400-83477600	Weak transcription	Primary B cells from cord blood	blood
31	chr15:83475600-83477000	Enhancers	Psoas Muscle	Psoas
32	chr15:83475600-83477000	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr15:83475600-83477800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr15:83475600-83478000	Enhancers	Fetal Muscle Leg	muscle
35	chr15:83475800-83477400	Weak transcription	Primary B cells from peripheral blood	blood
36	chr15:83476200-83477200	Weak transcription	Fetal Heart	heart
37	chr15:83476400-83476800	Weak transcription	GM12878-XiMat	blood
38	chr15:83476600-83477600	Enhancers	Right Atrium	heart
39	chr15:83476800-83477400	Enhancers	GM12878-XiMat	blood
40	chr15:83476800-83477600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr15:83477000-83477600	Weak transcription	Psoas Muscle	Psoas
42	chr15:83477000-83478000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr15:83477200-83477400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr15:83477200-83477400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr15:83477200-83477400	Enhancers	Fetal Heart	heart
46	chr15:83477200-83477400	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr15:83477200-83477400	Enhancers	Hela-S3	cervix
48	chr15:83477200-83477400	Flanking Bivalent TSS/Enh	HepG2	liver
49	chr15:83477200-83477400	Enhancers	K562	blood
50	chr15:83477200-83477800	Enhancers	H9 Cell Line	embryonic stem cell

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