Variant report

Variant	esv3342261
Chromosome Location	chr5:178053396-178055344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:545)
CpG islands
(count:550)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178052503-178054060	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178053514-178054047	K562	blood:	n/a	n/a
3	ATF1	chr5:178053891-178054277	K562	blood:	n/a	n/a
4	ATF2	chr5:178053813-178054238	H1-hESC	embryonic stem cell:	n/a	chr5:178054159-178054170
5	ATF3	chr5:178054011-178054203	H1-hESC	embryonic stem cell:	n/a	chr5:178054159-178054170 chr5:178054159-178054170 chr5:178054158-178054168 chr5:178054160-178054168
6	ATF3	chr5:178053850-178054207	K562	blood:	n/a	chr5:178054159-178054170 chr5:178054159-178054170 chr5:178054158-178054168 chr5:178054160-178054168
7	BACH1	chr5:178053382-178054434	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:178053118-178053503	K562	blood:	n/a	n/a
9	BATF	chr5:178053782-178054154	GM12878	blood:	n/a	n/a
10	BCL3	chr5:178053449-178054163	A549	lung:	n/a	n/a
11	BCLAF1	chr5:178053342-178054187	GM12878	blood:	n/a	n/a
12	BCLAF1	chr5:178053422-178054189	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:178052939-178054553	GM12878	blood:	n/a	chr5:178054543-178054552 chr5:178053688-178053704 chr5:178054544-178054553 chr5:178054544-178054553
14	BHLHE40	chr5:178053464-178054266	HepG2	liver:	n/a	chr5:178053688-178053704
15	BHLHE40	chr5:178052960-178054712	K562	blood:	n/a	chr5:178054543-178054552 chr5:178053688-178053704 chr5:178054544-178054553 chr5:178054538-178054559 chr5:178054544-178054553
16	BRCA1	chr5:178053649-178053758	HepG2	liver:	n/a	n/a
17	BRCA1	chr5:178053897-178054146	GM12878	blood:	n/a	n/a
18	BRCA1	chr5:178053423-178054220	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr5:178053388-178054227	K562	blood:	n/a	n/a
20	CBX3	chr5:178054231-178054818	K562	blood:	n/a	n/a
21	CBX3	chr5:178054229-178054657	K562	blood:	n/a	n/a
22	CCNT2	chr5:178053188-178054444	K562	blood:	n/a	chr5:178054346-178054355
23	CEBPB	chr5:178053003-178054315	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:178053938-178054197	K562	blood:	n/a	n/a
25	CEBPB	chr5:178052891-178053520	K562	blood:	n/a	n/a
26	CEBPB	chr5:178053061-178054351	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:178053992-178054551	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr5:178053018-178054327	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr5:178053918-178054322	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:178053570-178053791	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr5:178053783-178054330	K562	blood:	n/a	n/a
32	CEBPB	chr5:178054027-178054214	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:178053066-178053692	HepG2	liver:	n/a	n/a
34	CEBPD	chr5:178053893-178054472	HepG2	liver:	n/a	n/a
35	CEBPD	chr5:178053927-178054241	HepG2	liver:	n/a	n/a
36	CEBPD	chr5:178053782-178054292	K562	blood:	n/a	n/a
37	CHD1	chr5:178052674-178054612	GM12878	blood:	n/a	n/a
38	CHD1	chr5:178053248-178054059	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr5:178053380-178054436	HepG2	liver:	n/a	n/a
40	CHD2	chr5:178053415-178054122	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr5:178053213-178054448	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr5:178053310-178054439	K562	blood:	n/a	n/a
43	CHD2	chr5:178054349-178054552	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr5:178053062-178054547	GM12878	blood:	n/a	n/a
45	CREB1	chr5:178053393-178054423	GM12878	blood:	n/a	n/a
46	CREB1	chr5:178053801-178054519	A549	lung:	n/a	n/a
47	CREB1	chr5:178053417-178053798	A549	lung:	n/a	n/a
48	CREB1	chr5:178053856-178054349	ECC-1	luminal epithelium:	n/a	n/a
49	CREB1	chr5:178053316-178054434	HepG2	liver:	n/a	n/a
50	CREB1	chr5:178053703-178054385	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178054312-178054362	AG09309	skin:	n/a
2	chr5:178054312-178054362	AG09309	skin:	n/a
3	chr5:178053470-178053520	Jurkat	blood:	n/a
4	chr5:178053470-178053520	PrEC	prostate:	n/a
5	chr5:178054108-178054158	HAEpiC	amniotic membrane:	n/a
6	chr5:178054172-178054222	HAEpiC	amniotic membrane:	n/a
7	chr5:178054312-178054362	A549	lung:	n/a
8	chr5:178054312-178054362	HCT-116	colon:	n/a
9	chr5:178054172-178054222	ovcar-3	ovarian:	n/a
10	chr5:178054298-178054348	HCF	heart:	n/a
11	chr5:178054108-178054158	NT2-D1	testis:	n/a
12	chr5:178053533-178053583	A549	lung:	n/a
13	chr5:178053470-178053520	PFSK-1	brain:	n/a
14	chr5:178054039-178054089	SK-N-SH	brain:	n/a
15	chr5:178054172-178054222	PANC-1	pancreas:	n/a
16	chr5:178054312-178054362	MCF-7	breast:	n/a
17	chr5:178054039-178054089	Caco-2	colon:	n/a
18	chr5:178054039-178054089	AG04450	lung:	fetal
19	chr5:178054469-178054519	GM12892	blood:	n/a
20	chr5:178053533-178053583	CMK	blood:	n/a
21	chr5:178054039-178054089	SK-N-MC	brain:	n/a
22	chr5:178054172-178054222	BJ	skin:	n/a
23	chr5:178054298-178054348	GM06990	blood:	n/a
24	chr5:178054172-178054222	HEK293	kidney:	embryo
25	chr5:178054172-178054222	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:178054017-178054067	U87	brain:	n/a
27	chr5:178054017-178054067	BE2_C	brain:	n/a
28	chr5:178054039-178054089	AG09309	skin:	n/a
29	chr5:178053470-178053520	ovcar-3	ovarian:	n/a
30	chr5:178054017-178054067	HEK293	kidney:	embryo
31	chr5:178053533-178053583	HRE	kidney:	n/a
32	chr5:178054172-178054222	ECC-1	luminal epithelium:	n/a
33	chr5:178054108-178054158	IMR90	lung:	fetal
34	chr5:178054298-178054348	AG04450	lung:	fetal
35	chr5:178054039-178054089	Hepatocyte	liver:	n/a
36	chr5:178054039-178054089	NHBE	bronchial:	n/a
37	chr5:178054298-178054348	PANC-1	pancreas:	n/a
38	chr5:178054017-178054067	A549	lung:	n/a
39	chr5:178053470-178053520	A549	lung:	n/a
40	chr5:178054017-178054067	HMEC	breast:	n/a
41	chr5:178054298-178054348	GM12878	blood:	n/a
42	chr5:178054039-178054089	NHDF-neo	bronchial:	n/a
43	chr5:178054298-178054348	T-47D	breast:	n/a
44	chr5:178054469-178054519	HCT-116	colon:	n/a
45	chr5:178053533-178053583	RPTEC	kidney:	n/a
46	chr5:178054172-178054222	NH-A	brain:	n/a
47	chr5:178053533-178053583	PANC-1	pancreas:	n/a
48	chr5:178053533-178053583	SK-N-MC	brain:	n/a
49	chr5:178054017-178054067	HCT-116	colon:	n/a
50	chr5:178054172-178054222	MCF-7	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:16770750..16771264-chr5:178053613..178054437,2	HCT-116	colon:
2	chr12:7052986..7053545-chr5:178053747..178054708,2	Hela-S3	cervix:
3	chr5:178054153..178056905-chr5:178057584..178060537,3	K562	blood:
4	chr5:178053433..178053933-chrX:41193160..41193798,2	Hela-S3	cervix:
5	chr5:178052822..178055819-chr5:178156143..178158096,2	MCF-7	breast:
6	chr5:177659087..177660769-chr5:178052015..178054177,2	K562	blood:
7	chr5:178017082..178020481-chr5:178051764..178053531,4	MCF-7	breast:
8	chr5:178054261..178056030-chr5:178057503..178059124,2	MCF-7	breast:
9	chr5:177631376..177633067-chr5:178051942..178054079,2	K562	blood:
10	chr5:178019997..178022007-chr5:178050984..178053956,2	MCF-7	breast:
11	chr5:178052987..178056050-chr5:178056072..178058258,3	MCF-7	breast:
12	chr20:61568975..61569508-chr5:178053895..178054637,2	Hela-S3	cervix:
13	chr5:178051446..178054153-chr5:178157357..178158910,2	MCF-7	breast:
14	chr5:177631162..177632942-chr5:178051796..178054079,4	K562	blood:
15	chr5:178053026..178055082-chr6:26156240..26159025,2	MCF-7	breast:
16	chr5:178054847..178056678-chr5:178067285..178069085,2	K562	blood:
17	chr5:178053391..178055177-chr5:178285758..178288394,2	MCF-7	breast:
18	chr5:178050940..178053910-chr5:178263858..178266243,2	MCF-7	breast:

No data

Variant related genes	Relation type
CLK4	TF binding region
CLK4	CpG island
ENSG00000158373	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000101193	chromatin interactions
ENSG00000101191	chromatin interactions
ENSG00000175309	chromatin interactions
ENSG00000268790	chromatin interactions
ENSG00000178338	chromatin interactions
ENSG00000214046	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000169131	chromatin interactions
ENSG00000050767	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000215301	chromatin interactions
ENSG00000113240	chromatin interactions

Extended variants
information (count: 83 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:83 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563116134	chr5:178053408-178053409	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs11249554	chr5:178053487-178053488	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs189319396	chr5:178053495-178053496	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs548353671	chr5:178053500-178053501	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs557619025	chr5:178053554-178053555	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs57862544	chr5:178053560-178053561	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs114851608	chr5:178053587-178053588	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs556168854	chr5:178053625-178053626	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs574517218	chr5:178053637-178053638	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs541789875	chr5:178053658-178053659	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs546233141	chr5:178053673-178053674	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs527933898	chr5:178053684-178053685	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs546424680	chr5:178053699-178053700	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs111815874	chr5:178053708-178053709	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs71736243	chr5:178053709-178053710	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs139800222	chr5:178053728-178053729	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs531467755	chr5:178053755-178053756	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs377691710	chr5:178053808-178053809	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs182017847	chr5:178053857-178053858	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs13173605	chr5:178053898-178053899	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs369966863	chr5:178053900-178053901	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs60822440	chr5:178053912-178053913	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs565980167	chr5:178053914-178053915	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs373071165	chr5:178053942-178053943	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
25	rs557968809	chr5:178054001-178054002	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
26	rs548487415	chr5:178054028-178054029	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs568286793	chr5:178054041-178054042	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs556254694	chr5:178054065-178054066	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs574554241	chr5:178054077-178054078	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs6884172	chr5:178054178-178054179	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs553749162	chr5:178054211-178054212	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs186303542	chr5:178054216-178054217	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs565693378	chr5:178054219-178054220	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs199575451	chr5:178054223-178054224	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs59396780	chr5:178054224-178054225	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs373873313	chr5:178054225-178054226	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs371987488	chr5:178054256-178054257	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs546162782	chr5:178054266-178054267	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs564728950	chr5:178054273-178054274	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs143734037	chr5:178054286-178054287	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs190321459	chr5:178054299-178054300	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs113984225	chr5:178054311-178054312	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs543995325	chr5:178054370-178054371	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs538934028	chr5:178054387-178054388	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs6884657	chr5:178054405-178054406	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs528949335	chr5:178054408-178054409	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs547461908	chr5:178054410-178054411	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs569054137	chr5:178054441-178054442	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs73351824	chr5:178054459-178054460	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs73351825	chr5:178054477-178054478	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178051000-178053400	Flanking Active TSS	Primary T cells from cord blood	blood
2	chr5:178051000-178053400	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr5:178051000-178054400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:178051000-178054600	Active TSS	Breast Myoepithelial Primary Cells	Breast
5	chr5:178051200-178053400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
6	chr5:178051200-178053400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:178051200-178053400	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr5:178051200-178054600	Active TSS	Aorta	Aorta
9	chr5:178051400-178054400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr5:178051600-178054400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr5:178051600-178054600	Active TSS	NHDF-Ad	bronchial
12	chr5:178051600-178054600	Active TSS	NHLF	lung
13	chr5:178051800-178054600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr5:178051800-178054600	Active TSS	HSMM	muscle
15	chr5:178051800-178054800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:178052000-178054200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr5:178052000-178054200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
18	chr5:178052000-178054400	Active TSS	Fetal Intestine Large	intestine
19	chr5:178052000-178054400	Active TSS	Lung	lung
20	chr5:178052000-178054600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr5:178052000-178054600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr5:178052000-178054600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr5:178052000-178054600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr5:178052000-178054600	Active TSS	Cortex derived primary cultured neurospheres	brain
25	chr5:178052000-178054800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:178052000-178054800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr5:178052000-178054800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr5:178052200-178053400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr5:178052200-178054000	Bivalent/Poised TSS	HepG2	liver
30	chr5:178052200-178054400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr5:178052200-178054400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:178052200-178054400	Active TSS	HMEC	breast
33	chr5:178052200-178054600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr5:178052200-178054600	Active TSS	H9 Cell Line	embryonic stem cell
35	chr5:178052200-178054600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:178052200-178054600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:178052200-178054600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr5:178052200-178054600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr5:178052200-178054600	Active TSS	Esophagus	oesophagus
40	chr5:178052200-178054600	Active TSS	Fetal Heart	heart
41	chr5:178052200-178054600	Active TSS	Fetal Intestine Small	intestine
42	chr5:178052200-178054600	Active TSS	Fetal Kidney	kidney
43	chr5:178052200-178054800	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr5:178052200-178054800	Active TSS	Muscle Satellite Cultured Cells	--
45	chr5:178052200-178054800	Active TSS	Brain Anterior Caudate	brain
46	chr5:178052200-178054800	Active TSS	Colonic Mucosa	Colon
47	chr5:178052200-178054800	Active TSS	Colon Smooth Muscle	Colon
48	chr5:178052200-178054800	Active TSS	Fetal Brain Female	brain
49	chr5:178052200-178054800	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr5:178052200-178054800	Active TSS	NH-A	brain

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