Variant report

Variant	esv3315164
Chromosome Location	chr17:16573497-16587377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:16587344-16587522	HepG2	liver:	n/a	n/a
2	CEBPB	chr17:16574983-16575294	HepG2	liver:	n/a	chr17:16575111-16575124 chr17:16575113-16575124 chr17:16575111-16575122
3	CEBPB	chr17:16586409-16586499	IMR90	lung:	n/a	n/a
4	CEBPB	chr17:16586370-16586376	A549	lung:	n/a	n/a
5	CEBPB	chr17:16575013-16575369	IMR90	lung:	n/a	chr17:16575111-16575124 chr17:16575113-16575124 chr17:16575111-16575122
6	CEBPB	chr17:16582085-16582107	K562	blood:	n/a	n/a
7	CEBPB	chr17:16581042-16581078	A549	lung:	n/a	n/a
8	CEBPB	chr17:16575107-16575185	K562	blood:	n/a	chr17:16575111-16575124 chr17:16575113-16575124 chr17:16575111-16575122
9	CEBPB	chr17:16575057-16575363	A549	lung:	n/a	chr17:16575111-16575124 chr17:16575113-16575124 chr17:16575111-16575122
10	CHD2	chr17:16586678-16586885	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr17:16586756-16586911	HepG2	liver:	n/a	n/a
12	CTCF	chr17:16586640-16586790	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr17:16582022-16582101	GM10248	blood:	n/a	n/a
14	CTCF	chr17:16587029-16587082	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr17:16586680-16586830	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr17:16579100-16579111	GM20000	blood:	n/a	n/a
17	CTCF	chr17:16584954-16584991	LNCaP	prostate:	n/a	n/a
18	CTCF	chr17:16587120-16587270	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr17:16579116-16579157	GM20000	blood:	n/a	n/a
20	E2F6	chr17:16587017-16587258	H1-hESC	embryonic stem cell:	n/a	n/a
21	EP300	chr17:16580117-16580389	SK-N-SH_RA	brain:	n/a	n/a
22	ESR1	chr17:16575372-16575649	T-47D	breast:	n/a	chr17:16575501-16575518 chr17:16575500-16575517
23	ESR1	chr17:16575328-16575702	T-47D	breast:	n/a	chr17:16575501-16575518 chr17:16575500-16575517
24	FOXA1	chr17:16587216-16587512	HepG2	liver:	n/a	n/a
25	FOXA1	chr17:16587223-16587444	HepG2	liver:	n/a	n/a
26	FOXA1	chr17:16587188-16587482	HepG2	liver:	n/a	n/a
27	FOXA1	chr17:16587118-16587580	HepG2	liver:	n/a	n/a
28	FOXA2	chr17:16587269-16587459	HepG2	liver:	n/a	n/a
29	GATA3	chr17:16576448-16576645	SH-SY5Y	brain:	n/a	n/a
30	IRF3	chr17:16581319-16581457	GM12878	blood:	n/a	n/a
31	MAX	chr17:16587034-16587186	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAX	chr17:16587032-16587200	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYBL2	chr17:16587084-16587488	HepG2	liver:	n/a	n/a
34	POLR2A	chr17:16586744-16586915	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr17:16585359-16585591	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr17:16586673-16586847	K562	blood:	n/a	n/a
37	POLR2A	chr17:16584807-16584997	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr17:16586720-16587290	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr17:16584340-16584452	GM12878	blood:	n/a	n/a
40	POLR2A	chr17:16586727-16586868	A549	lung:	n/a	n/a
41	POLR2A	chr17:16584560-16584737	GM12878	blood:	n/a	n/a
42	POLR2A	chr17:16584845-16584963	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr17:16586750-16586831	A549	lung:	n/a	n/a
44	POLR2A	chr17:16586683-16586848	MCF-7	breast:	n/a	n/a
45	POLR2A	chr17:16587065-16587091	Gliobla	brain:	n/a	n/a
46	POLR2A	chr17:16582756-16582915	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr17:16587095-16587224	Gliobla	brain:	n/a	n/a
48	POLR2A	chr17:16586563-16587095	H1-hESC	embryonic stem cell:	n/a	n/a
49	RXRA	chr17:16587187-16587498	HepG2	liver:	n/a	n/a
50	SP1	chr17:16587115-16587578	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16587128-16587178	AoSMC	blood vessel:	n/a
2	chr17:16587128-16587178	MCF-7	breast:	n/a
3	chr17:16586857-16586907	Caco-2	colon:	n/a
4	chr17:16587128-16587178	HIPEpiC	eye:	n/a
5	chr17:16587128-16587178	HCF	heart:	n/a
6	chr17:16586857-16586907	HRPEpiC	eye:	n/a
7	chr17:16587128-16587178	HCM	heart:	n/a
8	chr17:16586857-16586907	IMR90	lung:	fetal
9	chr17:16587128-16587178	HRPEpiC	eye:	n/a
10	chr17:16587128-16587178	HCPEpiC	choroid plexus:	n/a
11	chr17:16586857-16586907	HEK293	kidney:	embryo
12	chr17:16587128-16587178	H1-hESC	embryonic stem cell:	embryo
13	chr17:16586857-16586907	HL-60	blood:	n/a
14	chr17:16586857-16586907	ovcar-3	ovarian:	n/a
15	chr17:16586857-16586907	BE2_C	brain:	n/a
16	chr17:16586857-16586907	NHBE	bronchial:	n/a
17	chr17:16586857-16586907	LNCaP	prostate:	n/a
18	chr17:16586857-16586907	ProgFib	skin:	n/a
19	chr17:16586857-16586907	HRE	kidney:	n/a
20	chr17:16587128-16587178	SKMC	muscle:	n/a
21	chr17:16587128-16587178	BE2_C	brain:	n/a
22	chr17:16587128-16587178	HEK293	kidney:	embryo
23	chr17:16586857-16586907	HMEC	breast:	n/a
24	chr17:16586857-16586907	HCPEpiC	choroid plexus:	n/a
25	chr17:16586857-16586907	NB4	blood:	n/a
26	chr17:16586857-16586907	Hepatocyte	liver:	n/a
27	chr17:16587128-16587178	ovcar-3	ovarian:	n/a
28	chr17:16586857-16586907	ECC-1	luminal epithelium:	n/a
29	chr17:16586857-16586907	NHDF-neo	bronchial:	n/a
30	chr17:16586857-16586907	SK-N-SH_RA	brain:	n/a
31	chr17:16586857-16586907	GM12892	blood:	n/a
32	chr17:16587128-16587178	GM06990	blood:	n/a
33	chr17:16586857-16586907	HIPEpiC	eye:	n/a
34	chr17:16587128-16587178	NT2-D1	testis:	n/a
35	chr17:16587128-16587178	LNCaP	prostate:	n/a
36	chr17:16586857-16586907	HPAEpiC	pulmonary alveolar:	n/a
37	chr17:16586857-16586907	AG04450	lung:	fetal
38	chr17:16587128-16587178	Hepatocyte	liver:	n/a
39	chr17:16586857-16586907	PANC-1	pancreas:	n/a
40	chr17:16587128-16587178	K562	blood:	n/a
41	chr17:16586857-16586907	HCT-116	colon:	n/a
42	chr17:16587128-16587178	HL-60	blood:	n/a
43	chr17:16586857-16586907	U87	brain:	n/a
44	chr17:16587128-16587178	NHBE	bronchial:	n/a
45	chr17:16587128-16587178	GM12892	blood:	n/a
46	chr17:16587128-16587178	HAEpiC	amniotic membrane:	n/a
47	chr17:16586857-16586907	MCF10A-Er-Src	breast:	n/a
48	chr17:16586857-16586907	SK-N-MC	brain:	n/a
49	chr17:16586857-16586907	HUVEC	blood vessel:	n/a
50	chr17:16587128-16587178	HEEpiC	esophagus:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:16556416..16558406-chr17:16573087..16576319,3	MCF-7	breast:
2	chr17:16555586..16557208-chr17:16578234..16580011,2	K562	blood:

No data

Variant related genes	Relation type
NEK4P2	TF binding region
RNASEH1P2	TF binding region
NEK4P2	CpG island
RNASEH1P2	CpG island
ENSG00000197566	chromatin interactions
ENSG00000264765	chromatin interactions

Extended variants
information (count: 504 )
Associated
traits (count: 158 )

Variant overlapped rSNPs/rCNVs (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191738172	chr17:16573530-16573531	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs114638642	chr17:16573560-16573561	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs140765923	chr17:16573568-16573569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs12939953	chr17:16573574-16573575	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546211634	chr17:16573591-16573592	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs570317454	chr17:16573606-16573607	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs75566280	chr17:16573620-16573621	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375623399	chr17:16573622-16573623	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs566098730	chr17:16573679-16573680	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576357287	chr17:16573694-16573695	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs201998227	chr17:16573740-16573741	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs112451481	chr17:16573753-16573754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs567207961	chr17:16573763-16573764	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs143202788	chr17:16573772-16573773	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs558968010	chr17:16573878-16573879	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs183256757	chr17:16574023-16574024	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs148266627	chr17:16574069-16574070	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs115583804	chr17:16574082-16574083	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530262939	chr17:16574090-16574091	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs76030202	chr17:16574091-16574092	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs141288739	chr17:16574318-16574319	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532093925	chr17:16574364-16574365	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs551878836	chr17:16574415-16574416	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs565717728	chr17:16574456-16574457	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs528172725	chr17:16574461-16574462	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187019598	chr17:16574503-16574504	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs189553013	chr17:16574600-16574601	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568227073	chr17:16574622-16574623	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs538085424	chr17:16574681-16574682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs554428712	chr17:16574717-16574718	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs113281567	chr17:16574725-16574726	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs557172318	chr17:16574795-16574796	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs377012698	chr17:16574869-16574870	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567865257	chr17:16574886-16574887	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs375439233	chr17:16574903-16574904	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs570664697	chr17:16574924-16574925	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs371273746	chr17:16574938-16574939	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs138072936	chr17:16574965-16574966	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs558674695	chr17:16575033-16575034	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs538294652	chr17:16575068-16575069	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs541109906	chr17:16575171-16575172	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs554668294	chr17:16575200-16575201	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs182250297	chr17:16575228-16575229	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs543667569	chr17:16575243-16575244	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs143915223	chr17:16575253-16575254	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs574991375	chr17:16575262-16575263	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs577465298	chr17:16575285-16575286	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs116031300	chr17:16575322-16575323	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs559072565	chr17:16575351-16575352	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs528109828	chr17:16575360-16575361	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:158)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16571000-16579600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr17:16579400-16580600	Enhancers	Fetal Stomach	stomach
3	chr17:16579600-16581000	Enhancers	Fetal Muscle Leg	muscle
4	chr17:16581000-16581800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr17:16581200-16581800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr17:16581400-16581800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr17:16581800-16589600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr17:16581800-16589800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr17:16583800-16584000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr17:16584000-16586800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr17:16585000-16586600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr17:16586400-16586600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr17:16586400-16587000	Weak transcription	Right Atrium	heart
14	chr17:16586400-16587000	Bivalent Enhancer	HepG2	liver
15	chr17:16586600-16586800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr17:16586600-16586800	Bivalent Enhancer	Fetal Brain Male	brain
17	chr17:16586600-16586800	Active TSS	Right Ventricle	heart
18	chr17:16586600-16586800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
19	chr17:16586600-16587000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr17:16586600-16587000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr17:16586600-16587000	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
22	chr17:16586600-16587000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr17:16586600-16587000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr17:16586600-16587000	Active TSS	Colon Smooth Muscle	Colon
25	chr17:16586600-16587000	Active TSS	Psoas Muscle	Psoas
26	chr17:16586600-16587000	Active TSS	HSMM	muscle
27	chr17:16586600-16587200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr17:16586600-16587200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr17:16586600-16587200	Active TSS	Brain Hippocampus Middle	brain
30	chr17:16586600-16587200	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr17:16586600-16587200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr17:16586600-16587400	Active TSS	Brain Substantia Nigra	brain
33	chr17:16586600-16587400	Bivalent/Poised TSS	Fetal Brain Female	brain
34	chr17:16586800-16587000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr17:16586800-16587000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr17:16586800-16587000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr17:16586800-16587000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
38	chr17:16586800-16587000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
39	chr17:16586800-16587000	Flanking Active TSS	Right Ventricle	heart
40	chr17:16586800-16587000	Bivalent/Poised TSS	NH-A	brain
41	chr17:16586800-16587200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr17:16586800-16587200	Bivalent Enhancer	Adipose Nuclei	Adipose
43	chr17:16586800-16587200	Active TSS	Brain Angular Gyrus	brain
44	chr17:16586800-16587200	Bivalent Enhancer	Left Ventricle	heart
45	chr17:16586800-16587400	Enhancers	Pancreas	Pancrea
46	chr17:16586800-16587400	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
47	chr17:16587000-16587200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr17:16587000-16587200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
49	chr17:16587000-16587400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr17:16587000-16587400	Bivalent Enhancer	Fetal Muscle Leg	muscle

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