Variant report

Variant	esv1818529
Chromosome Location	chr17:45583088-45683095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:815)
CpG islands
(count:428)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
2	BCLAF1	chr17:45609125-45609498	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
3	BHLHE40	chr17:45610659-45610881	HepG2	liver:	n/a	n/a
4	BHLHE40	chr17:45605793-45605974	HepG2	liver:	n/a	n/a
5	BRCA1	chr17:45682094-45682251	HepG2	liver:	n/a	n/a
6	CBX3	chr17:45609185-45609788	K562	blood:	n/a	n/a
7	CCNT2	chr17:45608329-45608370	K562	blood:	n/a	n/a
8	CEBPB	chr17:45644646-45644894	Hela-S3	cervix:	n/a	chr17:45644788-45644801
9	CEBPB	chr17:45665566-45665892	A549	lung:	n/a	n/a
10	CEBPB	chr17:45616089-45616461	K562	blood:	n/a	chr17:45616275-45616286
11	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
12	CEBPB	chr17:45589395-45589618	K562	blood:	n/a	n/a
13	CEBPB	chr17:45632282-45632410	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr17:45665577-45665788	HepG2	liver:	n/a	n/a
15	CEBPB	chr17:45616203-45616429	Hela-S3	cervix:	n/a	chr17:45616275-45616286
16	CEBPB	chr17:45616218-45616423	HepG2	liver:	n/a	chr17:45616275-45616286
17	CEBPB	chr17:45616205-45616431	K562	blood:	n/a	chr17:45616275-45616286
18	CEBPB	chr17:45616172-45616360	K562	blood:	n/a	chr17:45616275-45616286
19	CEBPB	chr17:45593807-45594016	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr17:45665580-45665831	IMR90	lung:	n/a	n/a
21	CEBPB	chr17:45589310-45589646	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr17:45616208-45616423	IMR90	lung:	n/a	chr17:45616275-45616286
23	CEBPB	chr17:45609557-45609591	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr17:45596411-45596603	IMR90	lung:	n/a	n/a
25	CEBPB	chr17:45665732-45665756	K562	blood:	n/a	n/a
26	CEBPB	chr17:45665734-45665783	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr17:45665734-45665763	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPD	chr17:45608348-45608658	HepG2	liver:	n/a	n/a
29	CHD2	chr17:45608212-45608501	HepG2	liver:	n/a	n/a
30	CHD2	chr17:45608171-45608525	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr17:45608212-45608653	A549	lung:	n/a	n/a
32	CTCF	chr17:45609146-45609247	GM19240	blood:	n/a	n/a
33	CTCF	chr17:45639787-45639938	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr17:45639600-45639750	HAc	cerebellar:	n/a	n/a
35	CTCF	chr17:45639653-45639953	A549	lung:	n/a	n/a
36	CTCF	chr17:45609163-45609272	GM10248	blood:	n/a	n/a
37	CTCF	chr17:45639800-45639917	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr17:45681326-45681405	GM19240	blood:	n/a	n/a
39	CTCF	chr17:45608677-45608717	Fibrobl	skin:	n/a	n/a
40	CTCF	chr17:45639939-45639941	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr17:45639821-45639905	GM13977	blood:	n/a	n/a
42	CTCF	chr17:45681300-45681450	Caco-2	colon:	n/a	n/a
43	CTCF	chr17:45669308-45669361	MCF-7	breast:	n/a	n/a
44	CTCF	chr17:45608264-45608280	GM13977	blood:	n/a	n/a
45	CTCF	chr17:45639691-45639984	K562	blood:	n/a	n/a
46	CTCF	chr17:45608670-45608672	MCF-7	breast:	n/a	n/a
47	CTCF	chr17:45639620-45639770	HepG2	liver:	n/a	n/a
48	CTCF	chr17:45639760-45639940	K562	blood:	n/a	n/a
49	CTCF	chr17:45639580-45639730	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr17:45639761-45639910	MCF-7	breast:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45608823-45608873	RPTEC	kidney:	n/a
2	chr17:45608823-45608873	RPTEC	kidney:	n/a
3	chr17:45681383-45681433	HCPEpiC	choroid plexus:	n/a
4	chr17:45612338-45612388	AG09309	skin:	n/a
5	chr17:45612338-45612388	NT2-D1	testis:	n/a
6	chr17:45604514-45604564	HUVEC	blood vessel:	n/a
7	chr17:45609121-45609171	HRCEpiC	kidney:	n/a
8	chr17:45612338-45612388	IMR90	lung:	fetal
9	chr17:45604514-45604564	T-47D	breast:	n/a
10	chr17:45612338-45612388	Caco-2	colon:	n/a
11	chr17:45612338-45612388	ovcar-3	ovarian:	n/a
12	chr17:45604514-45604564	ECC-1	luminal epithelium:	n/a
13	chr17:45609121-45609171	HepG2	liver:	n/a
14	chr17:45608114-45608164	PrEC	prostate:	n/a
15	chr17:45604514-45604564	HIPEpiC	eye:	n/a
16	chr17:45608114-45608164	AoSMC	blood vessel:	n/a
17	chr17:45604514-45604564	HepG2	liver:	n/a
18	chr17:45608315-45608365	CMK	blood:	n/a
19	chr17:45608114-45608164	NH-A	brain:	n/a
20	chr17:45608114-45608164	CMK	blood:	n/a
21	chr17:45608823-45608873	HRPEpiC	eye:	n/a
22	chr17:45608315-45608365	GM12878	blood:	n/a
23	chr17:45608114-45608164	HEK293	kidney:	embryo
24	chr17:45608114-45608164	HepG2	liver:	n/a
25	chr17:45608823-45608873	HCPEpiC	choroid plexus:	n/a
26	chr17:45681383-45681433	HUVEC	blood vessel:	n/a
27	chr17:45609121-45609171	SAEC	small airway:	n/a
28	chr17:45681383-45681433	LNCaP	prostate:	n/a
29	chr17:45681383-45681433	AoSMC	blood vessel:	n/a
30	chr17:45608315-45608365	LNCaP	prostate:	n/a
31	chr17:45604514-45604564	GM12878	blood:	n/a
32	chr17:45608823-45608873	HRCEpiC	kidney:	n/a
33	chr17:45604514-45604564	SK-N-MC	brain:	n/a
34	chr17:45681383-45681433	PrEC	prostate:	n/a
35	chr17:45604514-45604564	HMEC	breast:	n/a
36	chr17:45681383-45681433	HMEC	breast:	n/a
37	chr17:45608114-45608164	NHBE	bronchial:	n/a
38	chr17:45608114-45608164	HRCEpiC	kidney:	n/a
39	chr17:45608823-45608873	SK-N-SH	brain:	n/a
40	chr17:45681383-45681433	AG04449	skin:	fetal
41	chr17:45612338-45612388	AG04450	lung:	fetal
42	chr17:45681383-45681433	NHBE	bronchial:	n/a
43	chr17:45681383-45681433	AG10803	skin:	n/a
44	chr17:45612338-45612388	Jurkat	blood:	n/a
45	chr17:45681383-45681433	HNPCEpiC	eye:	n/a
46	chr17:45609121-45609171	ovcar-3	ovarian:	n/a
47	chr17:45609121-45609171	HEK293	kidney:	embryo
48	chr17:45604514-45604564	HCM	heart:	n/a
49	chr17:45608315-45608365	Caco-2	colon:	n/a
50	chr17:45681383-45681433	NB4	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
2	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:
3	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:
4	chr14:38063458..38065003-chr17:45607681..45609442,2	MCF-7	breast:
5	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:

No data

Variant related genes	Relation type
NPEPPS	TF binding region
ENSG00000206734	TF binding region
NPEPPS	CpG island
ENSG00000206734	CpG island
ENSG00000228782	chromatin interactions
ENSG00000141279	chromatin interactions
ENSG00000129514	chromatin interactions

Extended variants
information (count: 3291 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:3291 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566322163	chr17:45583109-45583110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191068649	chr17:45583230-45583231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554709562	chr17:45583231-45583232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs8074149	chr17:45583375-45583376	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs535970984	chr17:45583441-45583442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555838056	chr17:45583450-45583451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554396343	chr17:45583458-45583459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569747008	chr17:45583465-45583466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575997266	chr17:45583539-45583540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536705516	chr17:45583557-45583558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182860904	chr17:45583597-45583598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148299856	chr17:45583605-45583606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566614047	chr17:45583628-45583629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142855540	chr17:45583684-45583685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147439994	chr17:45583688-45583689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143675849	chr17:45583775-45583776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150533219	chr17:45583796-45583797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201794090	chr17:45583815-45583816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563793828	chr17:45583915-45583916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532410701	chr17:45583952-45583953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552495833	chr17:45583961-45583962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559812231	chr17:45583977-45583978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528795100	chr17:45584039-45584040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548451650	chr17:45584043-45584044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568362648	chr17:45584193-45584194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537240817	chr17:45584336-45584337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143887784	chr17:45584436-45584437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs62076553	chr17:45584458-45584459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569688286	chr17:45584551-45584552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538280099	chr17:45584705-45584706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558490966	chr17:45584751-45584752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572053295	chr17:45584814-45584815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114910307	chr17:45584851-45584852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554898280	chr17:45584866-45584867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111959896	chr17:45584888-45584889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186854415	chr17:45584908-45584909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543601312	chr17:45584931-45584932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11310394	chr17:45584963-45584964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563631670	chr17:45585007-45585008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577238511	chr17:45585019-45585020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545966217	chr17:45585021-45585022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143787192	chr17:45585075-45585076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528463997	chr17:45585084-45585085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374831009	chr17:45585132-45585133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548512042	chr17:45585230-45585231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140965306	chr17:45585271-45585272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374984478	chr17:45585335-45585336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374087027	chr17:45585434-45585435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528998939	chr17:45585499-45585500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs62077780	chr17:45585593-45585594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Medulloblastoma	21163964	CNVD
Epithelial cancer	20478067	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1433 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45579800-45589000	Weak transcription	Fetal Intestine Small	intestine
2	chr17:45580600-45583400	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr17:45580600-45589000	Weak transcription	K562	blood
4	chr17:45581000-45589000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr17:45582600-45589000	Weak transcription	Hela-S3	cervix
6	chr17:45583400-45585400	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr17:45585400-45589000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr17:45588800-45589000	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr17:45589000-45589200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr17:45589000-45589200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr17:45589000-45589200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr17:45589000-45589200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr17:45589000-45589200	Enhancers	Duodenum Mucosa	Duodenum
14	chr17:45589000-45589200	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr17:45589000-45589200	Enhancers	NHEK	skin
16	chr17:45589000-45589600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr17:45589000-45589600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr17:45589000-45589600	Enhancers	Primary B cells from peripheral blood	blood
19	chr17:45589000-45589600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr17:45589000-45589600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr17:45589000-45589600	Enhancers	Fetal Muscle Leg	muscle
22	chr17:45589000-45589600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
23	chr17:45589000-45589600	Flanking Active TSS	Hela-S3	cervix
24	chr17:45589000-45589600	Enhancers	HUVEC	blood vessel
25	chr17:45589000-45589600	Enhancers	K562	blood
26	chr17:45589000-45589600	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr17:45589000-45590000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr17:45589000-45590400	Enhancers	Fetal Intestine Small	intestine
29	chr17:45589000-45591200	Enhancers	Placenta	Placenta
30	chr17:45589200-45589400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr17:45589200-45589400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr17:45589200-45589400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr17:45589200-45589400	Enhancers	GM12878-XiMat	blood
34	chr17:45589200-45589600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr17:45589200-45589600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr17:45589200-45589600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr17:45589200-45589600	Enhancers	Primary hematopoietic stem cells	blood
38	chr17:45589200-45589600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr17:45589200-45589600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr17:45589200-45589600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr17:45589200-45589600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr17:45589200-45589600	Flanking Active TSS	Duodenum Mucosa	Duodenum
43	chr17:45589200-45589600	Enhancers	Fetal Lung	lung
44	chr17:45589200-45589600	Enhancers	Fetal Stomach	stomach
45	chr17:45589200-45589600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr17:45589200-45589600	Enhancers	A549	lung
47	chr17:45589200-45589600	Flanking Active TSS	NHEK	skin
48	chr17:45589200-45589600	Enhancers	Osteobl	bone
49	chr17:45589200-45590000	Enhancers	HMEC	breast
50	chr17:45589200-45590200	Enhancers	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links