Variant report

Variant	nsv976950
Chromosome Location	chr15:74888247-74891372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:414)
CpG islands
(count:183)
Chromatin interactive
region (count:7)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:28)

(count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74891088-74891138	HepG2	liver:	n/a	n/a
2	ATF2	chr15:74890561-74891228	GM12878	blood:	n/a	n/a
3	ATF2	chr15:74890529-74891187	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr15:74890510-74891363	GM12878	blood:	n/a	n/a
5	ATF2	chr15:74890483-74891099	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr15:74890625-74890895	HepG2	liver:	n/a	n/a
7	ATF3	chr15:74890503-74890971	GM12878	blood:	n/a	n/a
8	ATF3	chr15:74890518-74890918	K562	blood:	n/a	n/a
9	ATF3	chr15:74890530-74890911	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr15:74890485-74890934	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr15:74890612-74890870	GM12878	blood:	n/a	n/a
12	BACH1	chr15:74890814-74890950	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr15:74890704-74891161	A549	lung:	n/a	n/a
14	BCL3	chr15:74890435-74891273	GM12878	blood:	n/a	n/a
15	BCL3	chr15:74890610-74891125	GM12878	blood:	n/a	n/a
16	BCLAF1	chr15:74890430-74891366	GM12878	blood:	n/a	n/a
17	BCLAF1	chr15:74890526-74891196	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:74890478-74891136	K562	blood:	n/a	chr15:74890756-74890765 chr15:74890757-74890766 chr15:74890758-74890767 chr15:74890757-74890766 chr15:74890751-74890772
19	BHLHE40	chr15:74890558-74890921	GM12878	blood:	n/a	chr15:74890756-74890765 chr15:74890757-74890766 chr15:74890758-74890767 chr15:74890757-74890766 chr15:74890751-74890772
20	BHLHE40	chr15:74890513-74891094	HepG2	liver:	n/a	chr15:74890756-74890765 chr15:74890757-74890766 chr15:74890758-74890767 chr15:74890757-74890766 chr15:74890751-74890772
21	BRCA1	chr15:74890378-74890967	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr15:74890788-74890881	GM12878	blood:	n/a	n/a
23	CBX3	chr15:74890432-74891075	K562	blood:	n/a	n/a
24	CCNT2	chr15:74890601-74891467	K562	blood:	n/a	n/a
25	CEBPB	chr15:74890575-74891171	GM12878	blood:	n/a	n/a
26	CEBPD	chr15:74890646-74891024	HepG2	liver:	n/a	n/a
27	CEBPD	chr15:74890679-74890935	HepG2	liver:	n/a	n/a
28	CHD2	chr15:74890529-74891104	GM12878	blood:	n/a	n/a
29	CHD2	chr15:74890468-74891200	K562	blood:	n/a	n/a
30	CHD2	chr15:74890518-74891025	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr15:74890469-74890953	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr15:74890654-74891067	HepG2	liver:	n/a	n/a
33	CREB1	chr15:74890658-74891144	A549	lung:	n/a	n/a
34	CTCF	chr15:74891340-74891490	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr15:74888381-74888414	GM13976	blood:	n/a	n/a
36	CTCF	chr15:74890673-74891060	K562	blood:	n/a	n/a
37	CTCF	chr15:74890875-74890984	Lung_OC	lung:	n/a	n/a
38	CTCF	chr15:74890319-74890339	HepG2	liver:	n/a	n/a
39	CTCF	chr15:74890753-74890814	GM19239	blood:	n/a	n/a
40	E2F4	chr15:74890743-74890930	GM12878	blood:	n/a	n/a
41	E2F4	chr15:74890612-74891021	MCF10A-Er-Src	breast:	n/a	chr15:74890974-74890989
42	E2F4	chr15:74890559-74891079	K562	blood:	n/a	chr15:74890974-74890989
43	E2F6	chr15:74890521-74891318	A549	lung:	n/a	chr15:74890974-74890989
44	E2F6	chr15:74890361-74891388	K562	blood:	n/a	chr15:74890974-74890989
45	E2F6	chr15:74890584-74891055	K562	blood:	n/a	chr15:74890974-74890989
46	EBF1	chr15:74889856-74890243	GM12878	blood:	n/a	n/a
47	EBF1	chr15:74890667-74890867	GM12878	blood:	n/a	chr15:74890766-74890777
48	EGR1	chr15:74890433-74890756	K562	blood:	n/a	n/a
49	EGR1	chr15:74890428-74890776	K562	blood:	n/a	n/a
50	EGR1	chr15:74889091-74889416	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74891030-74891080	A549	lung:	n/a
2	chr15:74889327-74889377	SAEC	small airway:	n/a
3	chr15:74889327-74889377	H1-hESC	embryonic stem cell:	embryo
4	chr15:74889327-74889377	AG09319	gingival:	n/a
5	chr15:74891030-74891080	SK-N-SH	brain:	n/a
6	chr15:74891030-74891080	U87	brain:	n/a
7	chr15:74889327-74889377	NHBE	bronchial:	n/a
8	chr15:74889327-74889377	PFSK-1	brain:	n/a
9	chr15:74891030-74891080	H1-hESC	embryonic stem cell:	embryo
10	chr15:74889327-74889377	HMEC	breast:	n/a
11	chr15:74889327-74889377	MCF10A-Er-Src	breast:	n/a
12	chr15:74889327-74889377	SK-N-SH_RA	brain:	n/a
13	chr15:74891030-74891080	Hepatocyte	liver:	n/a
14	chr15:74889327-74889377	BE2_C	brain:	n/a
15	chr15:74891030-74891080	HCF	heart:	n/a
16	chr15:74889327-74889377	CMK	blood:	n/a
17	chr15:74891030-74891080	HCT-116	colon:	n/a
18	chr15:74891207-74891257	HEEpiC	esophagus:	n/a
19	chr15:74889327-74889377	PANC-1	pancreas:	n/a
20	chr15:74891030-74891080	NHDF-neo	bronchial:	n/a
21	chr15:74891207-74891257	PFSK-1	brain:	n/a
22	chr15:74891207-74891257	GM19239	blood:	n/a
23	chr15:74891207-74891257	ovcar-3	ovarian:	n/a
24	chr15:74891207-74891257	HAEpiC	amniotic membrane:	n/a
25	chr15:74891207-74891257	T-47D	breast:	n/a
26	chr15:74891030-74891080	PANC-1	pancreas:	n/a
27	chr15:74891030-74891080	HepG2	liver:	n/a
28	chr15:74891207-74891257	Jurkat	blood:	n/a
29	chr15:74891207-74891257	AoSMC	blood vessel:	n/a
30	chr15:74891030-74891080	Jurkat	blood:	n/a
31	chr15:74891030-74891080	HPAEpiC	pulmonary alveolar:	n/a
32	chr15:74891207-74891257	BE2_C	brain:	n/a
33	chr15:74889327-74889377	GM12891	blood:	n/a
34	chr15:74889327-74889377	HCF	heart:	n/a
35	chr15:74891030-74891080	HAEpiC	amniotic membrane:	n/a
36	chr15:74891030-74891080	T-47D	breast:	n/a
37	chr15:74891030-74891080	SKMC	muscle:	n/a
38	chr15:74889327-74889377	GM12878	blood:	n/a
39	chr15:74889327-74889377	HRCEpiC	kidney:	n/a
40	chr15:74891030-74891080	MCF-7	breast:	n/a
41	chr15:74891207-74891257	AG10803	skin:	n/a
42	chr15:74891207-74891257	HCT-116	colon:	n/a
43	chr15:74889327-74889377	NHDF-neo	bronchial:	n/a
44	chr15:74891207-74891257	K562	blood:	n/a
45	chr15:74891030-74891080	BE2_C	brain:	n/a
46	chr15:74891207-74891257	HRE	kidney:	n/a
47	chr15:74891207-74891257	AG09319	gingival:	n/a
48	chr15:74889327-74889377	HEK293	kidney:	embryo
49	chr15:74891030-74891080	Caco-2	colon:	n/a
50	chr15:74889327-74889377	NT2-D1	testis:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74891163..74893467-chr15:74893596..74895699,2	K562	blood:
2	chr15:74885278..74889186-chr15:74890286..74893326,4	K562	blood:
3	chr15:74882811..74885228-chr15:74890404..74892323,2	K562	blood:
4	chr15:74885692..74889192-chr15:74889315..74893477,4	MCF-7	breast:
5	chr15:74851516..74853661-chr15:74891010..74892976,2	K562	blood:
6	chr15:74885278..74889186-chr15:74890286..74893326,4	K562	blood:
7	chr15:74885692..74889192-chr15:74889315..74893477,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EDC3-6	chr15:74890869-74891092	NONHSAT047252
2	lnc-CLK3-1	chr15:74890841-74891878	NONHSAT047251
3	lnc-CLK3-2	chr15:74888937-74889259	NONHSAT047250
4	lnc-CLK3-2	chr15:74890122-74890318	NONHSAT047250

No data

(count:28 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ARID3B	hsa-let-7f-5p	chr15:74889769-74889775
2	ARID3B	hsa-let-7a-5p	chr15:74890445-74890464
3	ARID3B	hsa-miR-125b-5p	chr15:74890022-74890028
4	ARID3B	hsa-let-7a-5p	chr15:74889769-74889775
5	ARID3B	hsa-miR-125b-5p	chr15:74890008-74890029
6	ARID3B	hsa-miR-125b-5p	chr15:74888690-74888696
7	ARID3B	hsa-let-7b-5p	chr15:74890445-74890464
8	ARID3B	hsa-miR-125a-5p	chr15:74888333-74888339
9	ARID3B	hsa-let-7f-5p	chr15:74890457-74890463
10	ARID3B	hsa-miR-125b-5p	chr15:74889287-74889294
11	ARID3B	hsa-miR-125a-5p	chr15:74890006-74890029
12	ARID3B	hsa-let-7b-5p	chr15:74889048-74889054
13	ARID3B	hsa-let-7f-5p	chr15:74890367-74890373
14	ARID3B	hsa-miR-125b-5p	chr15:74889272-74889294
15	ARID3B	hsa-let-7b-5p	chr15:74889769-74889775
16	ARID3B	hsa-let-7b-5p	chr15:74890367-74890373
17	ARID3B	hsa-let-7a-5p	chr15:74890457-74890463
18	ARID3B	hsa-let-7b-5p	chr15:74890457-74890463
19	ARID3B	hsa-let-7a-5p	chr15:74890367-74890373
20	ARID3B	hsa-miR-125a-5p	chr15:74888690-74888696
21	ARID3B	hsa-let-7f-5p	chr15:74890445-74890464
22	ARID3B	hsa-miR-181d-5p	chr15:74890417-74890439
23	ARID3B	hsa-miR-125b-5p	chr15:74888333-74888339
24	ARID3B	hsa-miR-125a-5p	chr15:74890022-74890028
25	ARID3B	hsa-miR-125a-5p	chr15:74889272-74889294
26	ARID3B	hsa-let-7a-5p	chr15:74889048-74889054
27	ARID3B	hsa-miR-125a-5p	chr15:74889287-74889294
28	ARID3B	hsa-let-7f-5p	chr15:74889048-74889054

Variant related genes	Relation type
ARID3B	TF binding region
CLK3	TF binding region
ARID3B	CpG island
CLK3	CpG island
ENSG00000179335	chromatin interactions
ENSG00000179361	chromatin interactions

Extended variants
information (count: 114 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570715531	chr15:74888250-74888251	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs534754882	chr15:74888251-74888252	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs553041523	chr15:74888254-74888255	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs574924021	chr15:74888271-74888272	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs535459205	chr15:74888293-74888294	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs35873352	chr15:74888364-74888365	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs557341273	chr15:74888407-74888408	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs576228268	chr15:74888445-74888446	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs543742795	chr15:74888446-74888447	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs61192812	chr15:74888495-74888496	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs1044344	chr15:74888514-74888515	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs577101775	chr15:74888581-74888582	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs541272160	chr15:74888608-74888609	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs185172299	chr15:74888652-74888653	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs529827492	chr15:74888695-74888696	Weak transcription Strong transcription	TF binding region Chromatin interactive region miRNA target site	3 gene(s)	Overlapped CNVs	n/a
16	rs150314035	chr15:74888714-74888715	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs563320636	chr15:74888766-74888767	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs189889354	chr15:74888826-74888827	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs552462574	chr15:74888830-74888831	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs539761034	chr15:74888862-74888863	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs528660900	chr15:74888885-74888886	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs183868629	chr15:74888987-74888988	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs568426870	chr15:74888989-74888990	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs576966741	chr15:74888993-74888994	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs535965565	chr15:74889029-74889030	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs557025345	chr15:74889063-74889064	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs561210584	chr15:74889068-74889069	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs569242991	chr15:74889126-74889127	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs56663733	chr15:74889137-74889138	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs59860926	chr15:74889145-74889146	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs11072494	chr15:74889163-74889164	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs187173424	chr15:74889216-74889217	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs9707961	chr15:74889220-74889221	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs577235002	chr15:74889249-74889250	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs541208781	chr15:74889280-74889281	Weak transcription Strong transcription	TF binding region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
36	rs7496380	chr15:74889298-74889299	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs574423379	chr15:74889305-74889306	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs9707969	chr15:74889338-74889339	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs563098592	chr15:74889344-74889345	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs4887165	chr15:74889356-74889357	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs542170712	chr15:74889363-74889364	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545440396	chr15:74889500-74889501	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564418707	chr15:74889503-74889504	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372183689	chr15:74889534-74889535	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs528794801	chr15:74889551-74889552	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs546761946	chr15:74889552-74889553	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568641334	chr15:74889564-74889565	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529328355	chr15:74889598-74889599	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs149490636	chr15:74889602-74889603	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs569297878	chr15:74889618-74889619	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Intellectual disability	22102821	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
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Autism	20531469	CNVD

Chromatin state (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74840600-74890400	Weak transcription	Stomach Mucosa	stomach
2	chr15:74845800-74890400	Weak transcription	A549	lung
3	chr15:74854800-74888600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr15:74859000-74888600	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr15:74860400-74889000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr15:74860800-74888400	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr15:74861200-74889800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr15:74863600-74890800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr15:74863800-74890400	Weak transcription	Psoas Muscle	Psoas
10	chr15:74864400-74888400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr15:74866800-74890800	Weak transcription	Ovary	ovary
12	chr15:74876600-74888800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr15:74877400-74890400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr15:74877800-74888800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr15:74878000-74890200	Weak transcription	K562	blood
16	chr15:74878200-74888400	Strong transcription	Liver	Liver
17	chr15:74881000-74890400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr15:74881200-74888800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
19	chr15:74881200-74889600	Weak transcription	Fetal Heart	heart
20	chr15:74881200-74890400	Weak transcription	Fetal Kidney	kidney
21	chr15:74881200-74892200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:74881400-74888400	Strong transcription	Gastric	stomach
23	chr15:74881400-74889800	Strong transcription	Fetal Stomach	stomach
24	chr15:74881400-74890400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr15:74881400-74890400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:74881400-74890400	Weak transcription	Fetal Brain Male	brain
27	chr15:74881400-74892200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:74881600-74888400	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr15:74881600-74890400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr15:74881800-74888400	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr15:74881800-74888400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr15:74881800-74888400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:74881800-74888400	Strong transcription	Brain Cingulate Gyrus	brain
34	chr15:74881800-74888800	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr15:74881800-74888800	Strong transcription	Spleen	Spleen
36	chr15:74881800-74890400	Weak transcription	HSMM	muscle
37	chr15:74882000-74888400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:74882000-74890800	Weak transcription	Right Atrium	heart
39	chr15:74882200-74888400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr15:74882200-74888600	Strong transcription	Lung	lung
41	chr15:74882200-74890400	Weak transcription	NH-A	brain
42	chr15:74882400-74888400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:74882400-74888600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr15:74882400-74889800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr15:74882400-74890000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr15:74882600-74888400	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr15:74882600-74888400	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr15:74882600-74888400	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr15:74882600-74888400	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr15:74882600-74890200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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