Variant report

Variant	nsv4974
Chromosome Location	chr5:118750259-118795376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1153)
CpG islands
(count:1098)
Chromatin interactive
region (count:36)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1153 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118792192-118792337	K562	blood:	n/a	n/a
2	ARID3A	chr5:118788713-118788945	K562	blood:	n/a	n/a
3	ARID3A	chr5:118774954-118775053	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:118753728-118754183	K562	blood:	n/a	n/a
5	ARID3A	chr5:118788091-118788826	HepG2	liver:	n/a	n/a
6	ATF1	chr5:118787956-118788849	K562	blood:	n/a	n/a
7	ATF1	chr5:118774302-118774669	K562	blood:	n/a	n/a
8	ATF1	chr5:118753607-118754403	K562	blood:	n/a	n/a
9	ATF2	chr5:118787977-118788667	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:118787926-118788750	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr5:118787992-118788527	K562	blood:	n/a	chr5:118788349-118788358
12	BACH1	chr5:118752648-118752673	K562	blood:	n/a	n/a
13	BACH1	chr5:118788153-118788163	K562	blood:	n/a	n/a
14	BCLAF1	chr5:118753347-118754066	K562	blood:	n/a	chr5:118753556-118753565
15	BHLHE40	chr5:118771512-118771536	HepG2	liver:	n/a	n/a
16	BHLHE40	chr5:118787790-118788659	K562	blood:	n/a	n/a
17	BRCA1	chr5:118787732-118788698	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr5:118771171-118771188	GM12878	blood:	n/a	n/a
19	BRCA1	chr5:118788122-118788447	HepG2	liver:	n/a	n/a
20	BRCA1	chr5:118788373-118788813	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr5:118786556-118786843	K562	blood:	n/a	n/a
22	CBX3	chr5:118785593-118785980	K562	blood:	n/a	n/a
23	CBX3	chr5:118771130-118771583	K562	blood:	n/a	n/a
24	CBX3	chr5:118753507-118754103	K562	blood:	n/a	n/a
25	CBX3	chr5:118787133-118788713	K562	blood:	n/a	n/a
26	CBX3	chr5:118768458-118768725	K562	blood:	n/a	n/a
27	CBX3	chr5:118786296-118787121	K562	blood:	n/a	n/a
28	CCNT2	chr5:118774442-118774676	K562	blood:	n/a	n/a
29	CCNT2	chr5:118788090-118788668	K562	blood:	n/a	n/a
30	CEBPB	chr5:118774842-118775195	MCF-7	breast:	n/a	n/a
31	CEBPB	chr5:118774175-118774755	K562	blood:	n/a	chr5:118774521-118774532
32	CEBPB	chr5:118788469-118788736	HepG2	liver:	n/a	chr5:118788595-118788608 chr5:118788597-118788608 chr5:118788595-118788606
33	CEBPB	chr5:118788008-118788758	H1-hESC	embryonic stem cell:	n/a	chr5:118788595-118788608 chr5:118788597-118788608 chr5:118788595-118788606
34	CEBPB	chr5:118774909-118775121	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:118788415-118788783	A549	lung:	n/a	chr5:118788595-118788608 chr5:118788597-118788608 chr5:118788595-118788606
36	CEBPB	chr5:118788414-118788957	IMR90	lung:	n/a	chr5:118788595-118788608 chr5:118788597-118788608 chr5:118788595-118788606
37	CEBPB	chr5:118761724-118762088	K562	blood:	n/a	n/a
38	CEBPB	chr5:118763328-118763587	K562	blood:	n/a	n/a
39	CEBPB	chr5:118761783-118762108	K562	blood:	n/a	n/a
40	CEBPB	chr5:118753871-118754383	IMR90	lung:	n/a	chr5:118754059-118754072 chr5:118754059-118754070 chr5:118754058-118754075 chr5:118754060-118754071
41	CEBPB	chr5:118752466-118752650	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:118787851-118788960	HepG2	liver:	n/a	chr5:118788595-118788608 chr5:118788597-118788608 chr5:118788595-118788606
43	CEBPB	chr5:118774436-118774645	HepG2	liver:	n/a	chr5:118774521-118774532
44	CEBPB	chr5:118753645-118754462	K562	blood:	n/a	chr5:118754059-118754072 chr5:118754059-118754070 chr5:118754058-118754075 chr5:118754060-118754071
45	CEBPB	chr5:118753829-118754196	MCF-7	breast:	n/a	chr5:118754059-118754072 chr5:118754059-118754070 chr5:118754058-118754075 chr5:118754060-118754071
46	CEBPB	chr5:118753652-118754348	K562	blood:	n/a	chr5:118754059-118754072 chr5:118754059-118754070 chr5:118754058-118754075 chr5:118754060-118754071
47	CEBPB	chr5:118788367-118788787	MCF-7	breast:	n/a	chr5:118788595-118788608 chr5:118788597-118788608 chr5:118788595-118788606
48	CEBPB	chr5:118788277-118788906	A549	lung:	n/a	chr5:118788595-118788608 chr5:118788597-118788608 chr5:118788595-118788606
49	CEBPB	chr5:118763316-118763679	K562	blood:	n/a	n/a
50	CEBPB	chr5:118761742-118762000	K562	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118788746-118788796	Hela-S3	cervix:	n/a
2	chr5:118788128-118788178	GM12878	blood:	n/a
3	chr5:118787455-118787505	Hela-S3	cervix:	n/a
4	chr5:118787579-118787629	HRCEpiC	kidney:	n/a
5	chr5:118788352-118788402	LNCaP	prostate:	n/a
6	chr5:118788128-118788178	ovcar-3	ovarian:	n/a
7	chr5:118794305-118794355	U87	brain:	n/a
8	chr5:118788780-118788830	AG04450	lung:	fetal
9	chr5:118788229-118788279	NHDF-neo	bronchial:	n/a
10	chr5:118788780-118788830	PrEC	prostate:	n/a
11	chr5:118787579-118787629	ProgFib	skin:	n/a
12	chr5:118788644-118788694	AoSMC	blood vessel:	n/a
13	chr5:118788644-118788694	HCF	heart:	n/a
14	chr5:118787579-118787629	NT2-D1	testis:	n/a
15	chr5:118788137-118788187	H1-hESC	embryonic stem cell:	embryo
16	chr5:118785325-118785375	HRPEpiC	eye:	n/a
17	chr5:118791606-118791656	HIPEpiC	eye:	n/a
18	chr5:118788130-118788180	HAEpiC	amniotic membrane:	n/a
19	chr5:118788137-118788187	ProgFib	skin:	n/a
20	chr5:118788126-118788176	BE2_C	brain:	n/a
21	chr5:118788644-118788694	CMK	blood:	n/a
22	chr5:118788229-118788279	A549	lung:	n/a
23	chr5:118788644-118788694	MCF-7	breast:	n/a
24	chr5:118788126-118788176	HNPCEpiC	eye:	n/a
25	chr5:118788746-118788796	HAEpiC	amniotic membrane:	n/a
26	chr5:118788126-118788176	HCF	heart:	n/a
27	chr5:118788130-118788180	HepG2	liver:	n/a
28	chr5:118785325-118785375	H1-hESC	embryonic stem cell:	embryo
29	chr5:118788126-118788176	HRE	kidney:	n/a
30	chr5:118788746-118788796	HUVEC	blood vessel:	n/a
31	chr5:118785325-118785375	NH-A	brain:	n/a
32	chr5:118788126-118788176	LNCaP	prostate:	n/a
33	chr5:118788137-118788187	HEEpiC	esophagus:	n/a
34	chr5:118788137-118788187	SKMC	muscle:	n/a
35	chr5:118788291-118788341	NHBE	bronchial:	n/a
36	chr5:118788644-118788694	AG09309	skin:	n/a
37	chr5:118787985-118788035	Jurkat	blood:	n/a
38	chr5:118787579-118787629	MCF-7	breast:	n/a
39	chr5:118788644-118788694	GM19239	blood:	n/a
40	chr5:118788128-118788178	GM12892	blood:	n/a
41	chr5:118794305-118794355	NHDF-neo	bronchial:	n/a
42	chr5:118788137-118788187	AG10803	skin:	n/a
43	chr5:118794305-118794355	HepG2	liver:	n/a
44	chr5:118788126-118788176	H1-hESC	embryonic stem cell:	embryo
45	chr5:118788126-118788176	Caco-2	colon:	n/a
46	chr5:118787455-118787505	SK-N-SH_RA	brain:	n/a
47	chr5:118788720-118788770	HEK293	kidney:	embryo
48	chr5:118788229-118788279	PANC-1	pancreas:	n/a
49	chr5:118788130-118788180	HL-60	blood:	n/a
50	chr5:118788644-118788694	AG09319	gingival:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:118753692..118754236-chr6:26250478..26251239,2	NB4	blood:
2	chr5:118735386..118738101-chr5:118752192..118755044,3	K562	blood:
3	chr5:118408484..118411107-chr5:118751959..118754643,2	K562	blood:
4	chr5:118747162..118749496-chr5:118752473..118755239,2	K562	blood:
5	chr5:118787954..118788514-chr5:172197674..172198421,2	Hela-S3	cervix:
6	chr5:118405948..118407537-chr5:118753041..118754895,2	MCF-7	breast:
7	chr5:118754174..118756633-chr5:118758402..118759986,2	MCF-7	breast:
8	chr5:118603398..118605235-chr5:118750769..118753133,2	MCF-7	breast:
9	chr1:78148836..78149503-chr5:118753345..118754288,2	NB4	blood:
10	chr5:118753614..118755538-chr5:118867454..118869085,2	K562	blood:
11	chr5:118655474..118659015-chr5:118750147..118754859,4	K562	blood:
12	chr22:50354001..50354626-chr5:118788080..118788710,2	HCT-116	colon:
13	chr5:118323861..118326778-chr5:118787539..118789741,2	MCF-7	breast:
14	chr5:118629010..118630794-chr5:118752161..118754078,2	K562	blood:
15	chr5:118739304..118742654-chr5:118752620..118755578,3	K562	blood:
16	chr5:118753173..118755307-chr5:118768998..118771173,2	MCF-7	breast:
17	chr14:50359666..50360334-chr5:118787719..118788333,2	Hela-S3	cervix:
18	chr5:118788483..118791355-chr5:118802793..118805177,3	K562	blood:
19	chr5:118740750..118742654-chr5:118753714..118755578,2	K562	blood:
20	chr5:118754174..118756633-chr5:118758402..118759986,2	MCF-7	breast:
21	chr5:118323457..118324709-chr5:118770895..118771760,5	K562	blood:
22	chr5:118656369..118659015-chr5:118750147..118752975,4	K562	blood:
23	chr5:118323492..118324476-chr5:118770917..118771529,2	MCF-7	breast:
24	chr5:118783920..118786685-chr5:118788386..118791351,2	MCF-7	breast:
25	chr5:118784342..118786295-chr5:118788114..118789779,2	K562	blood:
26	chr5:118746206..118749496-chr5:118750368..118755239,5	K562	blood:
27	chr5:118787302..118789344-chr5:118814419..118817189,2	K562	blood:
28	chr5:118784342..118786376-chr5:118787907..118789779,3	K562	blood:
29	chr5:118745362..118747706-chr5:118750248..118751868,2	K562	blood:
30	chr5:118357331..118357914-chr5:118771263..118771765,2	K562	blood:
31	chr5:118760077..118762768-chr5:118762980..118764985,2	K562	blood:
32	chr5:118747505..118748328-chr5:118770657..118771776,5	MCF-7	breast:
33	chr5:118603215..118605720-chr5:118754635..118756360,2	MCF-7	breast:
34	chr5:118604990..118607098-chr5:118752315..118754043,2	K562	blood:
35	chr5:118760077..118762768-chr5:118762980..118764985,2	K562	blood:
36	chr5:118753173..118755307-chr5:118768998..118771173,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFAIP8-2	chr5:118792010-118792427	NONHSAT103435
2	lnc-TNFAIP8-2	chr5:118788461-118788516	NONHSAT103435

No data

Variant related genes	Relation type
RNA5SP190	TF binding region
HSD17B4	TF binding region
RNA5SP190	CpG island
HSD17B4	CpG island
ENSG00000145779	chromatin interactions
ENSG00000165527	chromatin interactions
ENSG00000036549	chromatin interactions
ENSG00000249494	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000198355	chromatin interactions
ENSG00000256316	chromatin interactions
ENSG00000172869	chromatin interactions
ENSG00000239084	chromatin interactions
ENSG00000169570	chromatin interactions
ENSG00000133835	chromatin interactions

Extended variants
information (count: 2166 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2166 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531056506	chr5:118750265-118750266	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs551119612	chr5:118750316-118750317	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs371731770	chr5:118750345-118750346	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs533173232	chr5:118750364-118750365	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs562180795	chr5:118750408-118750409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531090254	chr5:118750420-118750421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183010884	chr5:118750436-118750437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187605461	chr5:118750448-118750449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139899740	chr5:118750465-118750466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535087532	chr5:118750474-118750475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146835046	chr5:118750516-118750517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200254686	chr5:118750526-118750527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371258025	chr5:118750528-118750529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564696210	chr5:118750533-118750534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78887279	chr5:118750536-118750537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534631833	chr5:118750540-118750541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568531123	chr5:118750542-118750543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537513121	chr5:118750551-118750552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs151203304	chr5:118750573-118750574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368852838	chr5:118750629-118750630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115616406	chr5:118750653-118750654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569220088	chr5:118750656-118750657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117353451	chr5:118750666-118750667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553381861	chr5:118750677-118750678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112337864	chr5:118750699-118750700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541836311	chr5:118750701-118750702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555709868	chr5:118750734-118750735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530946351	chr5:118750846-118750847	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs193214070	chr5:118750914-118750915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs564576291	chr5:118750916-118750917	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184763588	chr5:118750934-118750935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112941824	chr5:118750946-118750947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76953400	chr5:118750994-118750995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs529156174	chr5:118750996-118750997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549020835	chr5:118751097-118751098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs372174148	chr5:118751103-118751104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568473137	chr5:118751110-118751111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187280685	chr5:118751121-118751122	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557426970	chr5:118751140-118751141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571051979	chr5:118751188-118751189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs150387031	chr5:118751191-118751192	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572225034	chr5:118751193-118751194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573379780	chr5:118751213-118751214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1995794	chr5:118751289-118751290	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs556108366	chr5:118751310-118751311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192221544	chr5:118751314-118751315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544666986	chr5:118751367-118751368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183939667	chr5:118751378-118751379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533492879	chr5:118751387-118751388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569300960	chr5:118751415-118751416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastric cancer	17229543	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118707600-118754600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:118747800-118753400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:118748000-118750400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr5:118748000-118750800	Enhancers	Primary B cells from cord blood	blood
5	chr5:118748000-118752200	Enhancers	Primary B cells from peripheral blood	blood
6	chr5:118748000-118752600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:118748000-118753600	Weak transcription	HMEC	breast
8	chr5:118748000-118753600	Weak transcription	NH-A	brain
9	chr5:118748000-118753800	Weak transcription	NHEK	skin
10	chr5:118748000-118754000	Weak transcription	Esophagus	oesophagus
11	chr5:118748000-118754400	Weak transcription	Placenta	Placenta
12	chr5:118748000-118755400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr5:118748200-118750400	Enhancers	Stomach Mucosa	stomach
14	chr5:118748200-118752600	Weak transcription	K562	blood
15	chr5:118748200-118753200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr5:118748200-118753200	Weak transcription	Dnd41	blood
17	chr5:118748200-118753400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr5:118748200-118753400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr5:118748200-118753600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:118748200-118753600	Weak transcription	Primary T cells from cord blood	blood
21	chr5:118748200-118753600	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr5:118748200-118753600	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr5:118748200-118753600	Weak transcription	Colon Smooth Muscle	Colon
24	chr5:118748200-118755000	Weak transcription	Liver	Liver
25	chr5:118748600-118753400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr5:118748800-118752600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr5:118748800-118753000	Weak transcription	Hela-S3	cervix
28	chr5:118748800-118753600	Weak transcription	Brain Angular Gyrus	brain
29	chr5:118748800-118753800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:118749200-118750400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr5:118749200-118750800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr5:118749800-118750400	Enhancers	Primary hematopoietic stem cells	blood
33	chr5:118749800-118750800	Enhancers	GM12878-XiMat	blood
34	chr5:118750000-118750400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr5:118750400-118752800	Weak transcription	Stomach Mucosa	stomach
36	chr5:118750400-118753200	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr5:118750400-118753400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:118750400-118753400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:118750400-118753800	Weak transcription	Primary hematopoietic stem cells	blood
40	chr5:118750800-118752600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr5:118750800-118753200	Weak transcription	Primary B cells from cord blood	blood
42	chr5:118752200-118753200	Weak transcription	Primary B cells from peripheral blood	blood
43	chr5:118752600-118752800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr5:118752600-118752800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr5:118752600-118753600	Enhancers	K562	blood
46	chr5:118752600-118756800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr5:118752800-118753200	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr5:118752800-118753600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:118752800-118754800	Enhancers	Stomach Mucosa	stomach
50	chr5:118753000-118754800	Enhancers	Hela-S3	cervix

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