Variant report

Variant	esv1814177
Chromosome Location	chr7:4825190-4842927
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:964)
CpG islands
(count:2076)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:4837777-4838043	K562	blood:	n/a	n/a
2	BACH1	chr7:4832282-4832726	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:4831795-4831907	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr7:4840478-4840998	GM12878	blood:	n/a	n/a
5	BCL3	chr7:4840452-4840927	GM12878	blood:	n/a	n/a
6	BCL3	chr7:4837795-4838210	A549	lung:	n/a	n/a
7	BHLHE40	chr7:4831699-4831994	K562	blood:	n/a	n/a
8	BHLHE40	chr7:4837800-4838000	K562	blood:	n/a	n/a
9	BHLHE40	chr7:4831700-4832012	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:4838912-4838913	HepG2	liver:	n/a	n/a
11	BRCA1	chr7:4837995-4838032	HepG2	liver:	n/a	n/a
12	CBX3	chr7:4831686-4832003	K562	blood:	n/a	n/a
13	CCNT2	chr7:4828356-4828609	K562	blood:	n/a	n/a
14	CCNT2	chr7:4831735-4832518	K562	blood:	n/a	n/a
15	CCNT2	chr7:4836586-4836786	K562	blood:	n/a	n/a
16	CCNT2	chr7:4827680-4827766	K562	blood:	n/a	n/a
17	CCNT2	chr7:4837767-4838677	K562	blood:	n/a	n/a
18	CEBPB	chr7:4834896-4835046	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:4837860-4838015	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:4826415-4826592	A549	lung:	n/a	n/a
21	CEBPB	chr7:4836040-4836252	IMR90	lung:	n/a	chr7:4836099-4836110
22	CEBPB	chr7:4835998-4836229	HepG2	liver:	n/a	chr7:4836099-4836110
23	CEBPB	chr7:4834867-4835072	K562	blood:	n/a	n/a
24	CEBPB	chr7:4834886-4834988	Hela-S3	cervix:	n/a	n/a
25	CHD1	chr7:4831797-4831893	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr7:4831765-4831860	K562	blood:	n/a	n/a
27	CHD2	chr7:4837931-4838131	K562	blood:	n/a	n/a
28	CHD2	chr7:4832640-4832815	GM12878	blood:	n/a	n/a
29	CHD2	chr7:4837806-4838073	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr7:4831748-4832128	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:4838033-4838102	HepG2	liver:	n/a	n/a
32	CHD2	chr7:4831784-4831963	HepG2	liver:	n/a	n/a
33	CHD2	chr7:4832371-4832708	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr7:4831642-4832532	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr7:4837779-4838110	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr7:4831644-4832405	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr7:4837736-4838048	A549	lung:	n/a	n/a
38	CTCF	chr7:4831780-4831930	HAc	cerebellar:	n/a	n/a
39	CTCF	chr7:4832462-4832512	Fibrobl	skin:	n/a	n/a
40	CTCF	chr7:4831800-4831950	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr7:4837750-4838239	A549	lung:	n/a	n/a
42	CTCF	chr7:4837820-4837970	HCM	heart:	n/a	n/a
43	CTCF	chr7:4837960-4838110	HAc	cerebellar:	n/a	n/a
44	CTCF	chr7:4837746-4838270	A549	lung:	n/a	n/a
45	CTCF	chr7:4837771-4838044	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr7:4837880-4838030	A549	lung:	n/a	n/a
47	CTCF	chr7:4831780-4831930	GM12865	blood:	n/a	n/a
48	CTCF	chr7:4831740-4831890	GM12875	blood:	n/a	n/a
49	CTCF	chr7:4837820-4837970	NHLF	lung:	n/a	n/a
50	CTCF	chr7:4831777-4831945	MCF-7	breast:	n/a	n/a

(count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4829256-4829306	HIPEpiC	eye:	n/a
2	chr7:4839495-4839545	ECC-1	luminal epithelium:	n/a
3	chr7:4829256-4829306	HIPEpiC	eye:	n/a
4	chr7:4839495-4839545	ECC-1	luminal epithelium:	n/a
5	chr7:4832359-4832409	AoSMC	blood vessel:	n/a
6	chr7:4832359-4832409	GM06990	blood:	n/a
7	chr7:4832359-4832409	U87	brain:	n/a
8	chr7:4841835-4841885	A549	lung:	n/a
9	chr7:4841435-4841485	HIPEpiC	eye:	n/a
10	chr7:4825255-4825305	MCF-7	breast:	n/a
11	chr7:4832340-4832390	HRPEpiC	eye:	n/a
12	chr7:4837925-4837975	HL-60	blood:	n/a
13	chr7:4832359-4832409	SKMC	muscle:	n/a
14	chr7:4841435-4841485	K562	blood:	n/a
15	chr7:4839097-4839147	A549	lung:	n/a
16	chr7:4831038-4831088	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:4837937-4837987	MCF-7	breast:	n/a
18	chr7:4827246-4827296	MCF-7	breast:	n/a
19	chr7:4832340-4832390	SK-N-SH	brain:	n/a
20	chr7:4831038-4831088	HCPEpiC	choroid plexus:	n/a
21	chr7:4839778-4839828	SK-N-SH_RA	brain:	n/a
22	chr7:4832174-4832224	NH-A	brain:	n/a
23	chr7:4841435-4841485	GM19239	blood:	n/a
24	chr7:4825336-4825386	AoSMC	blood vessel:	n/a
25	chr7:4830295-4830345	A549	lung:	n/a
26	chr7:4829256-4829306	HMEC	breast:	n/a
27	chr7:4837937-4837987	HRCEpiC	kidney:	n/a
28	chr7:4832359-4832409	HepG2	liver:	n/a
29	chr7:4836291-4836341	K562	blood:	n/a
30	chr7:4830907-4830957	HEK293	kidney:	embryo
31	chr7:4832340-4832390	AG09319	gingival:	n/a
32	chr7:4837937-4837987	Caco-2	colon:	n/a
33	chr7:4839025-4839075	HepG2	liver:	n/a
34	chr7:4827246-4827296	Jurkat	blood:	n/a
35	chr7:4831038-4831088	SK-N-MC	brain:	n/a
36	chr7:4828451-4828501	A549	lung:	n/a
37	chr7:4825336-4825386	NB4	blood:	n/a
38	chr7:4841339-4841389	PFSK-1	brain:	n/a
39	chr7:4837937-4837987	SAEC	small airway:	n/a
40	chr7:4834269-4834319	Caco-2	colon:	n/a
41	chr7:4839025-4839075	NT2-D1	testis:	n/a
42	chr7:4834269-4834319	BJ	skin:	n/a
43	chr7:4832535-4832585	GM12878	blood:	n/a
44	chr7:4834359-4834409	HCM	heart:	n/a
45	chr7:4830295-4830345	T-47D	breast:	n/a
46	chr7:4838902-4838952	HRCEpiC	kidney:	n/a
47	chr7:4828451-4828501	MCF10A-Er-Src	breast:	n/a
48	chr7:4828519-4828569	HEEpiC	esophagus:	n/a
49	chr7:4832535-4832585	NB4	blood:	n/a
50	chr7:4830402-4830452	MCF10A-Er-Src	breast:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4836661..4838749-chr7:4922252..4923951,34	MCF-7	breast:
2	chr7:4836973..4839244-chr7:4874732..4876620,2	K562	blood:
3	chr7:4821235..4827640-chr7:4827846..4833141,11	K562	blood:
4	chr7:4837705..4840224-chr7:4921777..4925523,3	K562	blood:
5	chr7:4837765..4838277-chr7:4869415..4870174,2	MCF-7	breast:
6	chr7:4823905..4827107-chr7:4829333..4833521,4	MCF-7	breast:
7	chr7:4837530..4838489-chr7:5124822..5125761,4	K562	blood:
8	chr7:4837470..4838008-chr7:5126525..5127159,2	K562	blood:
9	chr7:4841618..4843428-chr7:4844749..4846501,2	K562	blood:
10	chr7:4821235..4827640-chr7:4827846..4833141,11	K562	blood:
11	chr7:4838823..4839402-chr7:4922988..4923590,2	MCF-7	breast:
12	chr7:4828401..4832334-chr7:4833840..4840039,6	MCF-7	breast:
13	chr7:4830470..4833507-chr7:4836339..4839138,4	K562	blood:
14	chr7:4836637..4839193-chr7:4844147..4845682,2	K562	blood:
15	chr7:4837390..4838683-chr7:4923091..4923965,6	K562	blood:
16	chr7:4830470..4833507-chr7:4836339..4839138,4	K562	blood:
17	chr7:4837384..4838602-chr7:5124702..5125750,11	MCF-7	breast:
18	chr7:4836258..4838925-chr7:4843189..4845168,2	MCF-7	breast:
19	chr7:4815280..4818251-chr7:4830682..4833750,3	MCF-7	breast:
20	chr7:4795893..4798243-chr7:4822711..4825591,2	K562	blood:
21	chr7:4834373..4836925-chr7:4840140..4842359,2	K562	blood:
22	chr7:4836637..4838191-chr7:4844182..4846190,2	K562	blood:
23	chr7:4834373..4836925-chr7:4840140..4842359,2	K562	blood:
24	chr7:4815133..4816843-chr7:4827652..4829770,2	MCF-7	breast:
25	chr7:4836464..4838525-chr7:4860229..4862035,2	MCF-7	breast:
26	chr7:4650125..4650826-chr7:4837448..4838412,2	K562	blood:
27	chr7:4813279..4817996-chr7:4818432..4827499,15	MCF-7	breast:
28	chr7:4823905..4827107-chr7:4829333..4833521,4	MCF-7	breast:
29	chr7:4837541..4838410-chr7:5125029..5125763,4	MCF-7	breast:
30	chr7:4837975..4839568-chr7:4857330..4858935,2	MCF-7	breast:
31	chr7:4815302..4817443-chr7:4835837..4838194,2	MCF-7	breast:
32	chr7:4840473..4842887-chr7:4862690..4864291,2	K562	blood:
33	chr7:4831917..4833699-chr7:4922173..4923727,2	K562	blood:
34	chr7:4838244..4841077-chr7:4873411..4874965,2	MCF-7	breast:
35	chr7:4778391..4781100-chr7:4828582..4831115,2	K562	blood:
36	chr7:4837502..4838178-chr7:4889155..4889775,2	MCF-7	breast:
37	chr7:4820976..4822985-chr7:4824590..4827741,3	K562	blood:
38	chr7:4837509..4838249-chr7:5126592..5127103,2	MCF-7	breast:
39	chr7:4837132..4838836-chr7:4922824..4924030,19	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4656	chr7:4828239-4828261	MIMAT0019723

No data

Variant related genes	Relation type
AP5Z1	TF binding region
MIR4656	TF binding region
AP5Z1	CpG island
MIR4656	CpG island
ENSG00000242802	chromatin interactions
ENSG00000264474	chromatin interactions
ENSG00000164916	chromatin interactions
ENSG00000157927	chromatin interactions

Extended variants
information (count: 1601 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1601 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78461882	chr7:4825190-4825191	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs367981328	chr7:4825192-4825193	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs549733205	chr7:4825193-4825194	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs561646689	chr7:4825201-4825202	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs370469975	chr7:4825203-4825204	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs374687909	chr7:4825210-4825211	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs368559995	chr7:4825217-4825218	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs547137141	chr7:4825226-4825227	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs565769998	chr7:4825233-4825234	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs192441133	chr7:4825245-4825246	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs551568063	chr7:4825255-4825256	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs569547344	chr7:4825258-4825259	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs376671338	chr7:4825294-4825295	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs536924379	chr7:4825296-4825297	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs11772411	chr7:4825307-4825308	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs11768079	chr7:4825314-4825315	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs139019097	chr7:4825329-4825330	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs144563476	chr7:4825344-4825345	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs373873011	chr7:4825345-4825346	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs578065937	chr7:4825346-4825347	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs545239331	chr7:4825348-4825349	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs563857783	chr7:4825374-4825375	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs74274130	chr7:4825409-4825410	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs143028557	chr7:4825445-4825446	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs575938785	chr7:4825464-4825465	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs543341013	chr7:4825472-4825473	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs368330173	chr7:4825475-4825476	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs528847124	chr7:4825487-4825488	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs549062069	chr7:4825493-4825494	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs559147581	chr7:4825497-4825498	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs549294980	chr7:4825508-4825509	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs184442543	chr7:4825514-4825515	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs560873136	chr7:4825515-4825516	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs112250223	chr7:4825527-4825528	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs551212822	chr7:4825528-4825529	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs10230906	chr7:4825574-4825575	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs530654804	chr7:4825578-4825579	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs187364052	chr7:4825597-4825598	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs143694710	chr7:4825611-4825612	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs77641479	chr7:4825626-4825627	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs59177795	chr7:4825642-4825643	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs7801122	chr7:4825686-4825687	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs367870227	chr7:4825698-4825699	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs574312483	chr7:4825708-4825709	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs557536972	chr7:4825718-4825719	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs546591513	chr7:4825742-4825743	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs575899196	chr7:4825747-4825748	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs543246918	chr7:4825748-4825749	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs571549489	chr7:4825753-4825754	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs538533994	chr7:4825755-4825756	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4816000-4832000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:4816200-4832000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:4816200-4834400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:4816600-4830600	Weak transcription	Psoas Muscle	Psoas
5	chr7:4816600-4834800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:4816800-4826000	Weak transcription	NH-A	brain
7	chr7:4816800-4834400	Weak transcription	K562	blood
8	chr7:4816800-4834800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr7:4817000-4826000	Weak transcription	HMEC	breast
10	chr7:4817200-4832000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr7:4817400-4825600	Weak transcription	NHDF-Ad	bronchial
12	chr7:4817800-4830400	Weak transcription	Hela-S3	cervix
13	chr7:4818000-4831600	Weak transcription	Stomach Mucosa	stomach
14	chr7:4818200-4825800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr7:4818400-4831600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:4819200-4830400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:4819400-4830800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:4819600-4827600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr7:4819600-4831000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr7:4819600-4831400	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr7:4819600-4831400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:4819600-4831600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr7:4819600-4831600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:4819600-4831600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:4819600-4831600	Strong transcription	Fetal Intestine Small	intestine
26	chr7:4819600-4831600	Strong transcription	Fetal Stomach	stomach
27	chr7:4819800-4830400	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr7:4819800-4831600	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr7:4819800-4831800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:4819800-4832000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:4820200-4830200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:4820200-4831200	Strong transcription	Stomach Smooth Muscle	stomach
33	chr7:4820200-4831400	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr7:4820200-4831400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:4820200-4831400	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr7:4820200-4831400	Strong transcription	Fetal Thymus	thymus
37	chr7:4820200-4831400	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr7:4820200-4831600	Strong transcription	Primary B cells from peripheral blood	blood
39	chr7:4820200-4831600	Strong transcription	Primary T cells from cord blood	blood
40	chr7:4820200-4831600	Strong transcription	Thymus	Thymus
41	chr7:4820200-4832800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr7:4820200-4832800	Strong transcription	Dnd41	blood
43	chr7:4820400-4829400	Strong transcription	Adipose Nuclei	Adipose
44	chr7:4820400-4830800	Strong transcription	Brain Hippocampus Middle	brain
45	chr7:4820400-4831000	Strong transcription	Brain Angular Gyrus	brain
46	chr7:4820400-4831000	Strong transcription	Placenta	Placenta
47	chr7:4820400-4831200	Strong transcription	Fetal Muscle Trunk	muscle
48	chr7:4820400-4831200	Strong transcription	Left Ventricle	heart
49	chr7:4820400-4831400	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr7:4820400-4831400	Strong transcription	Rectal Mucosa Donor 29	rectum

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