Variant report

Variant	nsv1003217
Chromosome Location	chr3:81435044-81752521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1881)
CpG islands
(count:183)
Chromatin interactive
region (count:68)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1881 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:81725962-81726169	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:81715746-81715989	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:81733986-81734197	K562	blood:	n/a	n/a
4	ARID3A	chr3:81598568-81598974	K562	blood:	n/a	n/a
5	ARID3A	chr3:81512022-81512362	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:81539705-81539945	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:81510425-81510561	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:81734085-81734232	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:81715726-81716133	K562	blood:	n/a	n/a
10	ARID3A	chr3:81525030-81525184	K562	blood:	n/a	n/a
11	ATF1	chr3:81598619-81598832	K562	blood:	n/a	n/a
12	ATF1	chr3:81539694-81539966	K562	blood:	n/a	n/a
13	ATF1	chr3:81733898-81734200	K562	blood:	n/a	n/a
14	ATF2	chr3:81534488-81535060	GM12878	blood:	n/a	n/a
15	ATF2	chr3:81534486-81534931	GM12878	blood:	n/a	n/a
16	ATF2	chr3:81593386-81593921	GM12878	blood:	n/a	n/a
17	BACH1	chr3:81622912-81622914	K562	blood:	n/a	n/a
18	BACH1	chr3:81734002-81734181	K562	blood:	n/a	chr3:81734075-81734089
19	BATF	chr3:81606915-81607180	GM12878	blood:	n/a	n/a
20	BATF	chr3:81534550-81535092	GM12878	blood:	n/a	n/a
21	BATF	chr3:81717526-81717712	GM12878	blood:	n/a	chr3:81717629-81717640
22	BATF	chr3:81534486-81534834	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:81534515-81534856	GM12878	blood:	n/a	chr3:81534661-81534670
24	BCL3	chr3:81446181-81446476	GM12878	blood:	n/a	n/a
25	BCL3	chr3:81492969-81493465	A549	lung:	n/a	n/a
26	BCLAF1	chr3:81534447-81534951	GM12878	blood:	n/a	chr3:81534661-81534670 chr3:81534899-81534908
27	BHLHE40	chr3:81598621-81598872	K562	blood:	n/a	n/a
28	BHLHE40	chr3:81534564-81534857	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:81733962-81734242	K562	blood:	n/a	n/a
30	BRCA1	chr3:81693047-81693068	H1-hESC	embryonic stem cell:	n/a	n/a
31	CCNT2	chr3:81598585-81598820	K562	blood:	n/a	n/a
32	CCNT2	chr3:81689401-81689601	K562	blood:	n/a	n/a
33	CEBPB	chr3:81435365-81435840	HepG2	liver:	n/a	chr3:81435672-81435685 chr3:81435673-81435684
34	CEBPB	chr3:81541084-81541642	IMR90	lung:	n/a	chr3:81541270-81541283
35	CEBPB	chr3:81751672-81752056	HepG2	liver:	n/a	chr3:81751814-81751827 chr3:81751814-81751825 chr3:81751815-81751826 chr3:81751814-81751825 chr3:81751814-81751827 chr3:81751813-81751830
36	CEBPB	chr3:81594798-81595128	IMR90	lung:	n/a	n/a
37	CEBPB	chr3:81690893-81691087	K562	blood:	n/a	n/a
38	CEBPB	chr3:81552175-81552736	IMR90	lung:	n/a	chr3:81552320-81552331
39	CEBPB	chr3:81493093-81493402	A549	lung:	n/a	n/a
40	CEBPB	chr3:81492927-81493492	A549	lung:	n/a	n/a
41	CEBPB	chr3:81594909-81595089	A549	lung:	n/a	n/a
42	CEBPB	chr3:81539622-81540059	MCF-7	breast:	n/a	n/a
43	CEBPB	chr3:81493026-81493451	A549	lung:	n/a	n/a
44	CEBPB	chr3:81552187-81552422	A549	lung:	n/a	chr3:81552320-81552331
45	CEBPB	chr3:81748550-81748612	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:81539661-81540375	IMR90	lung:	n/a	n/a
47	CEBPB	chr3:81551523-81551723	K562	blood:	n/a	chr3:81551593-81551602 chr3:81551591-81551602 chr3:81551593-81551602 chr3:81551593-81551602 chr3:81551592-81551603 chr3:81551593-81551602 chr3:81551591-81551604 chr3:81551591-81551604
48	CEBPB	chr3:81621436-81621659	IMR90	lung:	n/a	chr3:81621520-81621531
49	CEBPB	chr3:81552175-81552499	HepG2	liver:	n/a	chr3:81552320-81552331
50	CEBPB	chr3:81539673-81540024	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:81533970-81534020	ProgFib	skin:	n/a
2	chr3:81604026-81604076	HL-60	blood:	n/a
3	chr3:81533970-81534020	SK-N-SH_RA	brain:	n/a
4	chr3:81604026-81604076	HRPEpiC	eye:	n/a
5	chr3:81533970-81534020	IMR90	lung:	fetal
6	chr3:81533970-81534020	HL-60	blood:	n/a
7	chr3:81604026-81604076	BE2_C	brain:	n/a
8	chr3:81604026-81604076	HCT-116	colon:	n/a
9	chr3:81533970-81534020	HEK293	kidney:	embryo
10	chr3:81604026-81604076	AG04449	skin:	fetal
11	chr3:81604026-81604076	CMK	blood:	n/a
12	chr3:81604026-81604076	Hepatocyte	liver:	n/a
13	chr3:81533970-81534020	Hela-S3	cervix:	n/a
14	chr3:81604026-81604076	HRE	kidney:	n/a
15	chr3:81540527-81540577	Hepatocyte	liver:	n/a
16	chr3:81540527-81540577	IMR90	lung:	fetal
17	chr3:81540527-81540577	PrEC	prostate:	n/a
18	chr3:81540527-81540577	HEK293	kidney:	embryo
19	chr3:81533970-81534020	SK-N-SH	brain:	n/a
20	chr3:81540527-81540577	GM12878	blood:	n/a
21	chr3:81540527-81540577	NB4	blood:	n/a
22	chr3:81533970-81534020	Hepatocyte	liver:	n/a
23	chr3:81604026-81604076	Jurkat	blood:	n/a
24	chr3:81540527-81540577	NHBE	bronchial:	n/a
25	chr3:81604026-81604076	HCPEpiC	choroid plexus:	n/a
26	chr3:81604026-81604076	SKMC	muscle:	n/a
27	chr3:81604026-81604076	BJ	skin:	n/a
28	chr3:81533970-81534020	U87	brain:	n/a
29	chr3:81604026-81604076	AG04450	lung:	fetal
30	chr3:81604026-81604076	MCF10A-Er-Src	breast:	n/a
31	chr3:81604026-81604076	K562	blood:	n/a
32	chr3:81540527-81540577	HEEpiC	esophagus:	n/a
33	chr3:81540527-81540577	HAEpiC	amniotic membrane:	n/a
34	chr3:81540527-81540577	SKMC	muscle:	n/a
35	chr3:81533970-81534020	HUVEC	blood vessel:	n/a
36	chr3:81604026-81604076	NHBE	bronchial:	n/a
37	chr3:81533970-81534020	HCT-116	colon:	n/a
38	chr3:81604026-81604076	PFSK-1	brain:	n/a
39	chr3:81540527-81540577	HCM	heart:	n/a
40	chr3:81533970-81534020	GM12892	blood:	n/a
41	chr3:81533970-81534020	LNCaP	prostate:	n/a
42	chr3:81540527-81540577	HepG2	liver:	n/a
43	chr3:81533970-81534020	HPAEpiC	pulmonary alveolar:	n/a
44	chr3:81540527-81540577	MCF10A-Er-Src	breast:	n/a
45	chr3:81540527-81540577	PFSK-1	brain:	n/a
46	chr3:81540527-81540577	AG10803	skin:	n/a
47	chr3:81604026-81604076	HRCEpiC	kidney:	n/a
48	chr3:81604026-81604076	HIPEpiC	eye:	n/a
49	chr3:81533970-81534020	GM19239	blood:	n/a
50	chr3:81604026-81604076	SK-N-MC	brain:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:81442949..81445413-chr3:81454355..81457016,2	K562	blood:
2	chr3:81717239..81719106-chr3:81808947..81811221,2	MCF-7	breast:
3	chr3:81497703..81499898-chr3:81516331..81519051,2	K562	blood:
4	chr17:57120862..57121542-chr3:81600136..81600921,2	MCF-7	breast:
5	chr3:81510208..81513532-chr3:81513585..81516903,3	K562	blood:
6	chr3:81721733..81724677-chr3:81809908..81812069,2	MCF-7	breast:
7	chr3:81499173..81502135-chr3:81503844..81505456,2	K562	blood:
8	chr3:81441048..81443684-chr3:81443916..81446774,2	MCF-7	breast:
9	chr3:81630870..81631818-chr3:81692664..81693573,4	MCF-7	breast:
10	chr3:81732924..81735042-chr3:81736495..81738777,2	MCF-7	breast:
11	chr3:81538877..81541023-chr3:81682087..81685020,2	MCF-7	breast:
12	chr3:81630866..81631772-chr3:82182178..82183039,2	MCF-7	breast:
13	chr3:81350858..81351477-chr3:81692810..81693343,2	MCF-7	breast:
14	chr3:81605753..81607787-chr3:81613884..81616486,2	MCF-7	breast:
15	chr3:81751412..81753231-chr3:81755307..81758066,3	K562	blood:
16	chr3:81630870..81631818-chr3:81692664..81693573,4	MCF-7	breast:
17	chr3:81596549..81599236-chr3:81601556..81604295,2	K562	blood:
18	chr17:56735051..56736577-chr3:81662286..81664124,2	MCF-7	breast:
19	chr3:81504098..81505685-chr3:180830013..180832749,2	MCF-7	breast:
20	chr3:81442949..81445413-chr3:81454355..81457016,2	K562	blood:
21	chr3:81630932..81631818-chr3:81692595..81693468,3	MCF-7	breast:
22	chr3:81660001..81661927-chr3:81662830..81664385,2	K562	blood:
23	chr12:104359580..104360355-chr3:81570763..81571263,2	NB4	blood:
24	chr3:81732924..81735042-chr3:81736495..81738777,2	MCF-7	breast:
25	chr3:81538877..81541023-chr3:81682087..81685020,2	MCF-7	breast:
26	chr3:81722096..81724371-chr3:81725223..81727466,2	MCF-7	breast:
27	chr3:81532629..81534291-chr3:81807934..81809803,2	MCF-7	breast:
28	chr3:81745236..81746984-chr3:81748340..81750520,2	K562	blood:
29	chr3:81607675..81609561-chr3:81976999..81978516,2	K562	blood:
30	chr3:81652021..81654582-chr3:81671146..81673581,2	MCF-7	breast:
31	chr3:81497118..81498955-chr3:81501852..81504094,2	K562	blood:
32	chr3:81605753..81607787-chr3:81613884..81616486,2	MCF-7	breast:
33	chr3:81609423..81612077-chr3:81612597..81614184,2	K562	blood:
34	chr3:81630932..81631818-chr3:81692595..81693468,3	MCF-7	breast:
35	chr3:81747836..81749687-chr3:81809960..81812581,3	K562	blood:
36	chr3:81497006..81498618-chr3:81501090..81503352,2	K562	blood:
37	chr3:81468010..81468642-chr3:81539494..81540060,2	MCF-7	breast:
38	chr3:81693699..81695612-chr3:81703909..81706890,2	MCF-7	breast:
39	chr3:81725205..81727443-chr3:81729973..81731776,2	K562	blood:
40	chr3:81725205..81727443-chr3:81729973..81731776,2	K562	blood:
41	chr3:81673093..81675788-chr3:81810671..81812507,2	K562	blood:
42	chr3:81706649..81709647-chr3:81713380..81715113,2	MCF-7	breast:
43	chr3:81706649..81709647-chr3:81713380..81715113,2	MCF-7	breast:
44	chr3:81468046..81468668-chr3:81630873..81631740,2	MCF-7	breast:
45	chr3:81468046..81468668-chr3:81630873..81631740,2	MCF-7	breast:
46	chr3:81722096..81724371-chr3:81725223..81727466,2	MCF-7	breast:
47	chr3:81596549..81599236-chr3:81601556..81604295,2	K562	blood:
48	chr3:81499173..81502135-chr3:81503844..81505456,2	K562	blood:
49	chr3:81402158..81403031-chr3:81466906..81467495,2	MCF-7	breast:
50	chr3:81652021..81654582-chr3:81671146..81673581,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CADM2-8	chr3:81597097-81598171	ENSG00000249130
2	lnc-ROBO1-7	chr3:81703730-81704152	NONHSAT090617
3	lnc-ROBO1-7	chr3:81719989-81720133	NONHSAT090617
4	lnc-CADM2-8	chr3:81598550-81598657	ENSG00000249130
5	lnc-CADM2-8	chr3:81597025-81598649	NONHSAT090615

No data

Variant related genes	Relation type
ENSG00000240404	TF binding region
RNU2-28P	TF binding region
SETP6	TF binding region
GBE1	TF binding region
ENSG00000240404	CpG island
RNU2-28P	CpG island
SETP6	CpG island
GBE1	CpG island
ENSG00000114480	chromatin interactions
ENSG00000139372	chromatin interactions
KIAA1598	miRNA target sites
SLC25A22	miRNA target sites

Extended variants
information (count: 10089 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:10089 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534048928	chr3:81435071-81435072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140264464	chr3:81435126-81435127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181309533	chr3:81435146-81435147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542501243	chr3:81435204-81435205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144103176	chr3:81435233-81435234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527738011	chr3:81435310-81435311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186307248	chr3:81435397-81435398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544572528	chr3:81435422-81435423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547434339	chr3:81435435-81435436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564110762	chr3:81435494-81435495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533169648	chr3:81435506-81435507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17018877	chr3:81435518-81435519	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573312382	chr3:81435530-81435531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560497296	chr3:81435552-81435553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529481294	chr3:81435558-81435559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs117388602	chr3:81435582-81435583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368640610	chr3:81435628-81435629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549347189	chr3:81435704-81435705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568915673	chr3:81435798-81435799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537518307	chr3:81435800-81435801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189933481	chr3:81435804-81435805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371248370	chr3:81435817-81435818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113141998	chr3:81435901-81435902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372830268	chr3:81435940-81435941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551518340	chr3:81435991-81435992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571223510	chr3:81436027-81436028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533771987	chr3:81436030-81436031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554103178	chr3:81436058-81436059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567487803	chr3:81436063-81436064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536427551	chr3:81436064-81436065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs276106	chr3:81436096-81436097	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs180805551	chr3:81436114-81436115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367777107	chr3:81436130-81436131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186527378	chr3:81436135-81436136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557838990	chr3:81436148-81436149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577613766	chr3:81436197-81436198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146477958	chr3:81436233-81436234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559779611	chr3:81436336-81436337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560398384	chr3:81436353-81436354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555750599	chr3:81436363-81436364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191028655	chr3:81436480-81436481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183825970	chr3:81436503-81436504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562909232	chr3:81436506-81436507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531944020	chr3:81436519-81436520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551451154	chr3:81436554-81436555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571410984	chr3:81436564-81436565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527266256	chr3:81436574-81436575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150175376	chr3:81436576-81436577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567528063	chr3:81436592-81436593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569978782	chr3:81436657-81436658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:2258 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81432800-81435400	Weak transcription	Fetal Brain Female	brain
2	chr3:81433000-81435600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:81435000-81435200	Enhancers	Fetal Brain Male	brain
4	chr3:81435000-81435800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:81435200-81435600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:81435200-81435600	Weak transcription	Fetal Brain Male	brain
7	chr3:81435400-81435600	Enhancers	Fetal Brain Female	brain
8	chr3:81435400-81436200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr3:81435600-81436400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr3:81435600-81437400	Enhancers	Fetal Brain Male	brain
11	chr3:81435800-81436600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr3:81436200-81446600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:81436400-81441400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr3:81437400-81442600	Weak transcription	Fetal Brain Male	brain
15	chr3:81439600-81440600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr3:81440000-81440400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:81441400-81445800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr3:81442000-81445200	Enhancers	Brain Germinal Matrix	brain
19	chr3:81442400-81442800	Enhancers	NH-A	brain
20	chr3:81442600-81443600	Enhancers	Brain Substantia Nigra	brain
21	chr3:81442600-81444000	Enhancers	Brain Anterior Caudate	brain
22	chr3:81442600-81444400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr3:81442600-81445000	Enhancers	Fetal Brain Female	brain
24	chr3:81442600-81445200	Enhancers	Fetal Brain Male	brain
25	chr3:81442800-81443200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr3:81443000-81444000	Enhancers	Brain Cingulate Gyrus	brain
27	chr3:81443200-81444000	Enhancers	Brain Angular Gyrus	brain
28	chr3:81445000-81445400	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr3:81455000-81455800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr3:81455200-81455600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr3:81455200-81455800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr3:81455200-81456000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr3:81455400-81455800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr3:81456000-81456600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr3:81456600-81456800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr3:81460000-81460400	Active TSS	A549	lung
37	chr3:81466800-81469000	Enhancers	Osteobl	bone
38	chr3:81467400-81468800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:81467600-81467800	Enhancers	Fetal Lung	lung
40	chr3:81467800-81469000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr3:81468800-81474400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr3:81469000-81474400	Weak transcription	Osteobl	bone
43	chr3:81469400-81469800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:81473400-81473600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:81473600-81474200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:81473600-81474400	Enhancers	HUVEC	blood vessel
47	chr3:81473600-81476200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr3:81473600-81476400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:81474000-81477400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr3:81474000-81477600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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