Variant report

Variant	nsv1033359
Chromosome Location	chr5:103989150-104157498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 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	BATF	chr5:104087746-104087944	GM12878	blood:	n/a	chr5:104087867-104087878
2	BATF	chr5:104087774-104088008	GM12878	blood:	n/a	chr5:104087867-104087878
3	CEBPB	chr5:104136255-104136426	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
4	CEBPB	chr5:104136228-104136514	Hela-S3	cervix:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
5	CEBPB	chr5:104038023-104038389	Hela-S3	cervix:	n/a	chr5:104038323-104038334
6	CEBPB	chr5:104136225-104136497	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
7	CEBPB	chr5:104136178-104136571	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
8	CEBPB	chr5:104136123-104136646	HCT-116	colon:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
9	CEBPB	chr5:104102566-104102783	HepG2	liver:	n/a	chr5:104102656-104102667
10	CEBPB	chr5:104068408-104068610	HepG2	liver:	n/a	chr5:104068507-104068518
11	CEBPB	chr5:104090393-104090670	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr5:104136188-104136569	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
13	CEBPB	chr5:104136117-104136616	MCF-7	breast:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
14	CEBPB	chr5:104136186-104136537	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
15	CEBPB	chr5:104136209-104136550	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
16	CEBPB	chr5:104136181-104136567	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
17	CEBPB	chr5:104136061-104136624	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
18	CEBPB	chr5:104136258-104136502	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
19	CEBPB	chr5:104102501-104102787	A549	lung:	n/a	chr5:104102656-104102667
20	CEBPB	chr5:104136032-104136689	MCF-7	breast:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
21	CEBPB	chr5:104136190-104136565	H1-hESC	embryonic stem cell:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
22	CEBPB	chr5:104136224-104136540	IMR90	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
23	CEBPB	chr5:104021885-104022145	A549	lung:	n/a	n/a
24	CEBPB	chr5:104136136-104136548	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
25	CEBPD	chr5:104136280-104136473	HepG2	liver:	n/a	n/a
26	CTCF	chr5:104069900-104070050	HBMEC	blood vessel:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
27	CTCF	chr5:104083629-104083642	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr5:104136280-104136430	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr5:104136252-104136452	GM10266	blood:	n/a	n/a
30	CTCF	chr5:104136280-104136430	GM12866	blood:	n/a	n/a
31	CTCF	chr5:104016442-104016544	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr5:104136314-104136381	GM19239	blood:	n/a	n/a
33	CTCF	chr5:104069920-104070070	HPF	lung:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
34	CTCF	chr5:104136280-104136430	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr5:104136178-104136467	T-47D	breast:	n/a	n/a
36	CTCF	chr5:104136280-104136430	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr5:104070060-104070210	GM12866	blood:	n/a	n/a
38	CTCF	chr5:104136205-104136484	Gliobla	brain:	n/a	n/a
39	CTCF	chr5:104136133-104136733	GM12878	blood:	n/a	n/a
40	CTCF	chr5:104136204-104136466	HepG2	liver:	n/a	n/a
41	CTCF	chr5:104069820-104069970	HCT-116	colon:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
42	CTCF	chr5:104072300-104072385	LNCaP	prostate:	n/a	n/a
43	CTCF	chr5:104063840-104063990	GM12864	blood:	n/a	n/a
44	CTCF	chr5:104136233-104136462	A549	lung:	n/a	n/a
45	CTCF	chr5:104136257-104136422	GM19240	blood:	n/a	n/a
46	CTCF	chr5:104136280-104136430	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr5:104136240-104136390	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr5:104136249-104136465	HepG2	liver:	n/a	n/a
49	CTCF	chr5:104118782-104118821	Medullo	brain:	n/a	n/a
50	CTCF	chr5:104069820-104069970	MCF-7	breast:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104090236-104090286	AG04449	skin:	fetal
2	chr5:104090236-104090286	Jurkat	blood:	n/a
3	chr5:104090236-104090286	K562	blood:	n/a
4	chr5:104090236-104090286	HRE	kidney:	n/a
5	chr5:104090236-104090286	NT2-D1	testis:	n/a
6	chr5:104090236-104090286	Hepatocyte	liver:	n/a
7	chr5:104090236-104090286	HCPEpiC	choroid plexus:	n/a
8	chr5:104090236-104090286	HEEpiC	esophagus:	n/a
9	chr5:104090236-104090286	GM12891	blood:	n/a
10	chr5:104090236-104090286	NHBE	bronchial:	n/a
11	chr5:104090236-104090286	SK-N-MC	brain:	n/a
12	chr5:104090236-104090286	SAEC	small airway:	n/a
13	chr5:104090236-104090286	NB4	blood:	n/a
14	chr5:104090236-104090286	LNCaP	prostate:	n/a
15	chr5:104090236-104090286	GM06990	blood:	n/a
16	chr5:104090236-104090286	U87	brain:	n/a
17	chr5:104090236-104090286	HRPEpiC	eye:	n/a
18	chr5:104090236-104090286	GM19239	blood:	n/a
19	chr5:104090236-104090286	HEK293	kidney:	embryo
20	chr5:104090236-104090286	SK-N-SH	brain:	n/a
21	chr5:104090236-104090286	AG09309	skin:	n/a
22	chr5:104090236-104090286	HIPEpiC	eye:	n/a
23	chr5:104090236-104090286	HRCEpiC	kidney:	n/a
24	chr5:104090236-104090286	HCM	heart:	n/a
25	chr5:104090236-104090286	AG04450	lung:	fetal
26	chr5:104090236-104090286	T-47D	breast:	n/a
27	chr5:104090236-104090286	SK-N-SH_RA	brain:	n/a
28	chr5:104090236-104090286	BJ	skin:	n/a
29	chr5:104090236-104090286	ECC-1	luminal epithelium:	n/a
30	chr5:104090236-104090286	PFSK-1	brain:	n/a
31	chr5:104090236-104090286	PrEC	prostate:	n/a
32	chr5:104090236-104090286	ovcar-3	ovarian:	n/a
33	chr5:104090236-104090286	AG10803	skin:	n/a
34	chr5:104090236-104090286	HMEC	breast:	n/a
35	chr5:104090236-104090286	CMK	blood:	n/a
36	chr5:104090236-104090286	HCT-116	colon:	n/a
37	chr5:104090236-104090286	ProgFib	skin:	n/a
38	chr5:104090236-104090286	HL-60	blood:	n/a
39	chr5:104090236-104090286	MCF10A-Er-Src	breast:	n/a
40	chr5:104090236-104090286	AoSMC	blood vessel:	n/a
41	chr5:104090236-104090286	HAEpiC	amniotic membrane:	n/a
42	chr5:104090236-104090286	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:104090236-104090286	IMR90	lung:	fetal
44	chr5:104090236-104090286	AG09319	gingival:	n/a
45	chr5:104090236-104090286	HepG2	liver:	n/a
46	chr5:104090236-104090286	A549	lung:	n/a
47	chr5:104090236-104090286	HCF	heart:	n/a
48	chr5:104090236-104090286	GM12892	blood:	n/a
49	chr5:104090236-104090286	HNPCEpiC	eye:	n/a
50	chr5:104090236-104090286	H1-hESC	embryonic stem cell:	embryo

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
2	chr5:103761403..103764401-chr5:103998452..104000157,2	MCF-7	breast:
3	chr5:104028054..104030764-chr5:104032138..104034804,2	K562	blood:
4	chr5:103985280..103987996-chr5:104035377..104038063,2	MCF-7	breast:
5	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
6	chr5:104033301..104035974-chr5:104038075..104040842,2	MCF-7	breast:
7	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
8	chr5:103984998..103987505-chr5:103990796..103992380,2	MCF-7	breast:
9	chr5:104028054..104030764-chr5:104032138..104034804,2	K562	blood:
10	chr5:104033301..104035974-chr5:104038075..104040842,2	MCF-7	breast:
11	chr5:103987247..103989988-chr5:103992385..103995079,2	MCF-7	breast:
12	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
13	chr5:103987247..103989988-chr5:103992385..103995079,2	MCF-7	breast:
14	chr5:104080992..104082950-chr5:104084605..104086219,2	K562	blood:
15	chr5:103812785..103815361-chr5:104049597..104051659,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-5	chr5:104074998-104075113	ENSG00000251574
2	lnc-C5orf30-2	chr5:104098977-104099084	XLOC_004497
3	lnc-NUDT12-5	chr5:104080291-104080310	NONHSAT103088
4	lnc-C5orf30-3	chr5:104109342-104109441	ENSG00000253776
5	lnc-NUDT12-5	chr5:104109314-104109485	ENSG00000251574
6	lnc-C5orf30-2	chr5:104079736-104079888	XLOC_004497
7	lnc-NUDT12-5	chr5:104052350-104052364	NONHSAT103081
8	lnc-NUDT12-5	chr5:104079393-104079555	ENSG00000251574
9	lnc-NUDT12-5	chr5:104109314-104109492	ENSG00000251574
10	lnc-NUDT12-13	chr5:104137254-104137422	l_2988_chr5:104103131-104137422_testes
11	lnc-NUDT12-5	chr5:104075198-104075242	ENSG00000251574
12	lnc-NUDT12-5	chr5:104082242-104082310	ENSG00000251574
13	lnc-NUDT12-13	chr5:104118423-104118445	l_2988_chr5:104103131-104137422_testes
14	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
15	lnc-NUDT12-5	chr5:104079736-104079892	ENSG00000251574
16	lnc-NUDT12-13	chr5:104103132-104103235	l_2988_chr5:104103131-104137422_testes
17	lnc-NUDT12-5	chr5:104074955-104075113	ENSG00000251574
18	lnc-NUDT12-5	chr5:104075198-104075336	ENSG00000251574
19	lnc-NUDT12-5	chr5:104074962-104075113	ENSG00000251574
20	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103082
21	lnc-NUDT12-5	chr5:104081064-104081147	NONHSAT103088
22	lnc-NUDT12-5	chr5:104052350-104052364	NONHSAT103082
23	lnc-NUDT12-5	chr5:104072462-104072616	ENSG00000251574
24	lnc-NUDT12-5	chr5:104109434-104109523	ENSG00000251574
25	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
26	lnc-NUDT12-5	chr5:104109314-104109397	ENSG00000251574
27	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
28	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103082
29	lnc-NUDT12-5	chr5:104109314-104109361	ENSG00000251574
30	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
31	lnc-NUDT12-5	chr5:104098932-104099084	ENSG00000251574
32	lnc-NUDT12-5	chr5:104075198-104075336	ENSG00000251574
33	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103088
34	lnc-NUDT12-5	chr5:104109434-104109524	NONHSAT103081
35	lnc-C5orf30-3	chr5:104135007-104135473	ENSG00000253776
36	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103081

No data

Variant related genes	Relation type
ENSG00000253776	TF binding region
RNU6-334P	TF binding region
ENSG00000251574	TF binding region
ENSG00000253776	CpG island
RNU6-334P	CpG island
ENSG00000251574	CpG island
ENSG00000251574	chromatin interactions
CREB3L2	miRNA target sites

Extended variants
information (count: 2229 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2229 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79683209	chr5:103989152-103989153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375718154	chr5:103989182-103989183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs193186537	chr5:103989185-103989186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541643296	chr5:103989205-103989206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs59541105	chr5:103989225-103989226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561964453	chr5:103989282-103989283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547781330	chr5:103989288-103989289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532296808	chr5:103989315-103989316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558957697	chr5:103989332-103989333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371262329	chr5:103989333-103989334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564106864	chr5:103989335-103989336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370043566	chr5:103989391-103989392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563691035	chr5:103989443-103989444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs57228618	chr5:103989465-103989466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552825058	chr5:103989468-103989469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532784573	chr5:103989481-103989482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549428362	chr5:103989482-103989483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs58171504	chr5:103989486-103989487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569393199	chr5:103989513-103989514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374069656	chr5:103989584-103989585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549310790	chr5:103989587-103989588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566306018	chr5:103989617-103989618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544698753	chr5:103989645-103989646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375915420	chr5:103989664-103989665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146511842	chr5:103989668-103989669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552434102	chr5:103989688-103989689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs74811865	chr5:103989720-103989721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557426323	chr5:103989725-103989726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187343242	chr5:103989734-103989735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141152915	chr5:103989753-103989754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35999857	chr5:103989792-103989793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370912801	chr5:103989806-103989807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533276264	chr5:103989886-103989887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191800778	chr5:103989894-103989895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549843726	chr5:103989914-103989915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570747833	chr5:103989922-103989923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373249487	chr5:103989923-103989924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564053538	chr5:103989940-103989941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559102962	chr5:103989948-103989949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144742990	chr5:103989987-103989988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542990893	chr5:103990003-103990004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184013104	chr5:103990028-103990029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114780404	chr5:103990043-103990044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12189083	chr5:103990057-103990058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs370897100	chr5:103990075-103990076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559645774	chr5:103990095-103990096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574305879	chr5:103990113-103990114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552070331	chr5:103990115-103990116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571955281	chr5:103990118-103990119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368217428	chr5:103990121-103990122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Retinoblastoma	22278416	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
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103988600-103990200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr5:103992000-103992200	Enhancers	Rectal Smooth Muscle	rectum
3	chr5:103992200-103995200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr5:103992400-103996400	Weak transcription	Colon Smooth Muscle	Colon
5	chr5:103995200-103996000	Enhancers	Rectal Smooth Muscle	rectum
6	chr5:103995200-103996600	Enhancers	HUVEC	blood vessel
7	chr5:103996000-103997000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr5:103996400-103997800	Enhancers	Colon Smooth Muscle	Colon
9	chr5:103997000-103997200	Enhancers	Rectal Smooth Muscle	rectum
10	chr5:104023800-104024600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:104033800-104035000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:104033800-104035200	ZNF genes & repeats	Adipose Nuclei	Adipose
13	chr5:104034000-104035200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:104034200-104035000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:104034800-104035200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
16	chr5:104035200-104036000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:104036200-104037000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:104040600-104041800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:104041000-104041600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr5:104041000-104041600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr5:104041200-104041600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:104041400-104042000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr5:104042000-104045800	Enhancers	HUVEC	blood vessel
24	chr5:104042400-104042800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:104043800-104044000	Enhancers	Rectal Smooth Muscle	rectum
26	chr5:104044800-104045000	Enhancers	Rectal Smooth Muscle	rectum
27	chr5:104049400-104049800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr5:104049800-104051200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:104051200-104053000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:104052000-104052600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:104065400-104065800	Enhancers	Rectal Smooth Muscle	rectum
32	chr5:104065800-104066200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr5:104065800-104067800	Enhancers	Fetal Lung	lung
34	chr5:104066200-104066400	Enhancers	Rectal Smooth Muscle	rectum
35	chr5:104066400-104067600	Weak transcription	Rectal Smooth Muscle	rectum
36	chr5:104067200-104067600	Enhancers	Colon Smooth Muscle	Colon
37	chr5:104067600-104068200	Enhancers	Rectal Smooth Muscle	rectum
38	chr5:104067600-104069200	Weak transcription	Colon Smooth Muscle	Colon
39	chr5:104068200-104068600	Weak transcription	Rectal Smooth Muscle	rectum
40	chr5:104068600-104070200	Enhancers	Rectal Smooth Muscle	rectum
41	chr5:104069200-104070200	Enhancers	Colon Smooth Muscle	Colon
42	chr5:104089600-104090800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr5:104089800-104090000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:104089800-104090200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr5:104089800-104091200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr5:104089800-104091200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr5:104089800-104091200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr5:104089800-104091200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr5:104089800-104091400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:104090000-104090600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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