Variant report

Variant	esv2761819
Chromosome Location	chr14:20577698-20677591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:496)
CpG islands
(count:549)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20645562-20646086	K562	blood:	n/a	n/a
2	ARID3A	chr14:20584982-20585271	K562	blood:	n/a	n/a
3	ARID3A	chr14:20644582-20645133	K562	blood:	n/a	n/a
4	ATF1	chr14:20608626-20608778	K562	blood:	n/a	n/a
5	ATF1	chr14:20645594-20645932	K562	blood:	n/a	n/a
6	ATF1	chr14:20584956-20585164	K562	blood:	n/a	n/a
7	ATF3	chr14:20584968-20585229	K562	blood:	n/a	n/a
8	ATF3	chr14:20638032-20638356	K562	blood:	n/a	n/a
9	ATF3	chr14:20645584-20645910	K562	blood:	n/a	n/a
10	BACH1	chr14:20584638-20585505	K562	blood:	n/a	n/a
11	BHLHE40	chr14:20645542-20646303	K562	blood:	n/a	n/a
12	BHLHE40	chr14:20653018-20653080	K562	blood:	n/a	n/a
13	CBX3	chr14:20586942-20587293	K562	blood:	n/a	n/a
14	CBX3	chr14:20645515-20645980	K562	blood:	n/a	n/a
15	CBX3	chr14:20584916-20585201	K562	blood:	n/a	n/a
16	CBX3	chr14:20645492-20645863	K562	blood:	n/a	n/a
17	CBX3	chr14:20632642-20632904	K562	blood:	n/a	n/a
18	CBX3	chr14:20586982-20587337	K562	blood:	n/a	n/a
19	CBX3	chr14:20632656-20632932	K562	blood:	n/a	n/a
20	CCNT2	chr14:20645714-20646195	K562	blood:	n/a	n/a
21	CEBPB	chr14:20645527-20645985	K562	blood:	n/a	n/a
22	CEBPB	chr14:20667315-20667568	K562	blood:	n/a	chr14:20667443-20667454
23	CEBPB	chr14:20668546-20668738	A549	lung:	n/a	n/a
24	CEBPB	chr14:20578686-20578922	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:20652454-20652480	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:20645573-20645988	K562	blood:	n/a	n/a
27	CEBPB	chr14:20667271-20667577	Hela-S3	cervix:	n/a	chr14:20667443-20667454
28	CEBPB	chr14:20644548-20644852	K562	blood:	n/a	chr14:20644780-20644791 chr14:20644718-20644735 chr14:20644780-20644791
29	CEBPB	chr14:20638948-20639275	HepG2	liver:	n/a	chr14:20639103-20639114
30	CEBPB	chr14:20667315-20667616	A549	lung:	n/a	chr14:20667443-20667454
31	CEBPB	chr14:20643233-20643506	K562	blood:	n/a	chr14:20643311-20643324
32	CEBPB	chr14:20638926-20639276	K562	blood:	n/a	chr14:20639103-20639114
33	CEBPB	chr14:20644555-20644849	K562	blood:	n/a	chr14:20644780-20644791 chr14:20644718-20644735 chr14:20644780-20644791
34	CEBPB	chr14:20578612-20578943	IMR90	lung:	n/a	n/a
35	CEBPB	chr14:20622449-20622660	HepG2	liver:	n/a	chr14:20622561-20622572
36	CEBPB	chr14:20639049-20639270	IMR90	lung:	n/a	chr14:20639103-20639114
37	CEBPB	chr14:20578620-20578945	K562	blood:	n/a	n/a
38	CEBPB	chr14:20659063-20659394	HepG2	liver:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
39	CEBPB	chr14:20634808-20635061	HepG2	liver:	n/a	chr14:20634950-20634963 chr14:20634951-20634962 chr14:20634950-20634961 chr14:20634952-20634961
40	CEBPB	chr14:20584757-20585090	K562	blood:	n/a	n/a
41	CEBPB	chr14:20668608-20668745	K562	blood:	n/a	n/a
42	CEBPB	chr14:20659170-20659372	K562	blood:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
43	CEBPB	chr14:20578626-20578939	A549	lung:	n/a	n/a
44	CEBPB	chr14:20638951-20639274	A549	lung:	n/a	chr14:20639103-20639114
45	CEBPB	chr14:20631110-20631224	HepG2	liver:	n/a	chr14:20631171-20631182
46	CEBPB	chr14:20578635-20578967	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:20667283-20667629	HepG2	liver:	n/a	chr14:20667443-20667454
48	CEBPB	chr14:20618584-20618626	A549	lung:	n/a	n/a
49	CEBPD	chr14:20645568-20646098	K562	blood:	n/a	n/a
50	CEBPD	chr14:20645540-20645977	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20586367-20586417	SAEC	small airway:	n/a
2	chr14:20664580-20664630	CMK	blood:	n/a
3	chr14:20611779-20611829	K562	blood:	n/a
4	chr14:20585753-20585803	HNPCEpiC	eye:	n/a
5	chr14:20611779-20611829	HCPEpiC	choroid plexus:	n/a
6	chr14:20586367-20586417	HMEC	breast:	n/a
7	chr14:20664021-20664071	MCF-7	breast:	n/a
8	chr14:20611696-20611746	Hepatocyte	liver:	n/a
9	chr14:20586367-20586417	HCT-116	colon:	n/a
10	chr14:20612220-20612270	Caco-2	colon:	n/a
11	chr14:20611779-20611829	ovcar-3	ovarian:	n/a
12	chr14:20666088-20666138	MCF10A-Er-Src	breast:	n/a
13	chr14:20584239-20584289	BJ	skin:	n/a
14	chr14:20611696-20611746	GM12892	blood:	n/a
15	chr14:20585753-20585803	GM12892	blood:	n/a
16	chr14:20584239-20584289	AG09319	gingival:	n/a
17	chr14:20585753-20585803	GM12891	blood:	n/a
18	chr14:20584239-20584289	AG04449	skin:	fetal
19	chr14:20586367-20586417	HPAEpiC	pulmonary alveolar:	n/a
20	chr14:20664021-20664071	HRE	kidney:	n/a
21	chr14:20612220-20612270	HCT-116	colon:	n/a
22	chr14:20666088-20666138	AG04450	lung:	fetal
23	chr14:20584239-20584289	GM12878	blood:	n/a
24	chr14:20586367-20586417	LNCaP	prostate:	n/a
25	chr14:20664021-20664071	HCM	heart:	n/a
26	chr14:20585753-20585803	AG09309	skin:	n/a
27	chr14:20666088-20666138	HIPEpiC	eye:	n/a
28	chr14:20664580-20664630	LNCaP	prostate:	n/a
29	chr14:20664021-20664071	GM19239	blood:	n/a
30	chr14:20586367-20586417	HCM	heart:	n/a
31	chr14:20586367-20586417	AG10803	skin:	n/a
32	chr14:20584239-20584289	ECC-1	luminal epithelium:	n/a
33	chr14:20585753-20585803	Hepatocyte	liver:	n/a
34	chr14:20611779-20611829	NB4	blood:	n/a
35	chr14:20611696-20611746	PrEC	prostate:	n/a
36	chr14:20611779-20611829	MCF-7	breast:	n/a
37	chr14:20611779-20611829	AoSMC	blood vessel:	n/a
38	chr14:20666088-20666138	BJ	skin:	n/a
39	chr14:20585753-20585803	GM06990	blood:	n/a
40	chr14:20584239-20584289	HAEpiC	amniotic membrane:	n/a
41	chr14:20664580-20664630	RPTEC	kidney:	n/a
42	chr14:20664021-20664071	RPTEC	kidney:	n/a
43	chr14:20584239-20584289	MCF-7	breast:	n/a
44	chr14:20585753-20585803	K562	blood:	n/a
45	chr14:20666088-20666138	HCF	heart:	n/a
46	chr14:20585753-20585803	Hela-S3	cervix:	n/a
47	chr14:20666088-20666138	GM12892	blood:	n/a
48	chr14:20612220-20612270	SK-N-SH_RA	brain:	n/a
49	chr14:20586367-20586417	U87	brain:	n/a
50	chr14:20611779-20611829	RPTEC	kidney:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20623957..20624479-chr3:64655642..64656615,2	MCF-7	breast:
2	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
3	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
4	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
5	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
6	chr14:20615947..20618319-chr14:20622650..20625486,3	K562	blood:
7	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
8	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
9	chr14:20645875..20648132-chr14:20651152..20653312,3	K562	blood:
10	chr14:20583619..20586533-chr14:20649310..20650931,2	K562	blood:
11	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
12	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
13	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
14	chr14:20642540..20645135-chr14:20796578..20798741,2	K562	blood:
15	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
16	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
17	chr14:20615947..20618319-chr14:20622650..20625017,2	K562	blood:
18	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
19	chr14:20582658..20584245-chr14:20584576..20586426,2	K562	blood:
20	chr14:20645666..20648683-chr14:20649468..20653312,5	K562	blood:
21	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
22	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
23	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4N5-1	chr14:20617391-20617904	NONHSAT035552

No data

Variant related genes	Relation type
OR4N5	TF binding region
OR4K17	TF binding region
OR11H5P	TF binding region
RNA5SP381	TF binding region
OR11G1P	TF binding region
OR11G2	TF binding region
ENSG00000259095	TF binding region
PSMB7P1	TF binding region
OR4N5	CpG island
OR4K17	CpG island
OR11H5P	CpG island
RNA5SP381	CpG island
OR11G1P	CpG island
OR11G2	CpG island
ENSG00000259095	CpG island
PSMB7P1	CpG island
ENSG00000184394	chromatin interactions
ENSG00000258468	chromatin interactions
ENSG00000259074	chromatin interactions
ENSG00000100814	chromatin interactions
ENSG00000176230	chromatin interactions

Extended variants
information (count: 1793 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1793 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146602848	chr14:20580555-20580556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149199178	chr14:20580569-20580570	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs17093690	chr14:20580570-20580571	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs79225363	chr14:20580577-20580578	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs143389255	chr14:20580621-20580622	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs187201240	chr14:20580627-20580628	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs532287939	chr14:20580675-20580676	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs550695497	chr14:20580679-20580680	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs371195609	chr14:20580687-20580688	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs372311989	chr14:20580705-20580706	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs568927968	chr14:20580709-20580710	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs537663422	chr14:20580725-20580726	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs555651923	chr14:20580748-20580749	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs567975113	chr14:20580818-20580819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534989242	chr14:20580821-20580822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78155252	chr14:20580836-20580837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148379034	chr14:20580840-20580841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538601475	chr14:20580844-20580845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141389554	chr14:20580890-20580891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575614747	chr14:20580920-20580921	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs542830229	chr14:20580921-20580922	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs377137581	chr14:20580951-20580952	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561738696	chr14:20581018-20581019	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs573125934	chr14:20581040-20581041	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs540147426	chr14:20581050-20581051	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs147041643	chr14:20581085-20581086	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs191141738	chr14:20581107-20581108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550555985	chr14:20581149-20581150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562589823	chr14:20581190-20581191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183846596	chr14:20581239-20581240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549586931	chr14:20581266-20581267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188279406	chr14:20581276-20581277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535372950	chr14:20581288-20581289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373025123	chr14:20581292-20581293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193284947	chr14:20581296-20581297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74037240	chr14:20581317-20581318	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs372787975	chr14:20581345-20581346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538662855	chr14:20581360-20581361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184755873	chr14:20581362-20581363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575721775	chr14:20581372-20581373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536333330	chr14:20581446-20581447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573811630	chr14:20581459-20581460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554789732	chr14:20581559-20581560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138359795	chr14:20581599-20581600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187632379	chr14:20581687-20581688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565189523	chr14:20581770-20581771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112557022	chr14:20581788-20581789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77276880	chr14:20581808-20581809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191299568	chr14:20581884-20581885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562451358	chr14:20581898-20581899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20580400-20580800	Enhancers	K562	blood
2	chr14:20580800-20584200	Weak transcription	K562	blood
3	chr14:20584200-20584600	Enhancers	K562	blood
4	chr14:20584600-20585000	Flanking Active TSS	K562	blood
5	chr14:20585000-20585200	Enhancers	K562	blood
6	chr14:20585200-20585400	Flanking Active TSS	K562	blood
7	chr14:20585400-20585600	Enhancers	K562	blood
8	chr14:20585400-20585800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr14:20585600-20585800	ZNF genes & repeats	K562	blood
10	chr14:20585800-20586400	Genic enhancers	K562	blood
11	chr14:20586200-20586600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:20586400-20586600	Enhancers	K562	blood
13	chr14:20611200-20612600	Enhancers	K562	blood
14	chr14:20612400-20612800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:20613200-20613400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr14:20613600-20621000	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr14:20622200-20622400	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr14:20623000-20624000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr14:20630600-20630800	ZNF genes & repeats	Pancreas	Pancrea
20	chr14:20638000-20638800	Enhancers	K562	blood
21	chr14:20638400-20638600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr14:20638400-20638800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr14:20638800-20643000	Weak transcription	K562	blood
24	chr14:20643000-20644000	Enhancers	K562	blood
25	chr14:20643400-20643600	Enhancers	Pancreas	Pancrea
26	chr14:20643400-20643800	Enhancers	Stomach Mucosa	stomach
27	chr14:20643800-20645200	Weak transcription	Pancreas	Pancrea
28	chr14:20644000-20644200	Flanking Active TSS	K562	blood
29	chr14:20644200-20644400	Enhancers	Stomach Mucosa	stomach
30	chr14:20644200-20644600	Enhancers	K562	blood
31	chr14:20644600-20644800	Flanking Active TSS	K562	blood
32	chr14:20644800-20645000	Enhancers	K562	blood
33	chr14:20645000-20645200	Flanking Active TSS	K562	blood
34	chr14:20645200-20645800	Enhancers	K562	blood
35	chr14:20645200-20646400	Enhancers	Pancreas	Pancrea
36	chr14:20645800-20646400	Flanking Active TSS	K562	blood
37	chr14:20646000-20648200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr14:20646000-20649000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr14:20646200-20646400	Enhancers	Primary hematopoietic stem cells	blood
40	chr14:20646400-20647400	Weak transcription	Pancreas	Pancrea
41	chr14:20646400-20648400	Enhancers	K562	blood
42	chr14:20646800-20647400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr14:20647000-20647800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr14:20647400-20647600	ZNF genes & repeats	Pancreas	Pancrea
45	chr14:20647400-20648200	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr14:20647400-20648400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr14:20647600-20648200	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr14:20647600-20650400	Weak transcription	Pancreas	Pancrea
49	chr14:20647800-20648200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
50	chr14:20648000-20648400	Enhancers	Primary hematopoietic stem cells	blood

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