Variant report

Variant	esv3422518
Chromosome Location	chr7:97910041-97912589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97910130-97910572	HepG2	liver:	n/a	n/a
2	ATF3	chr7:97910761-97911014	K562	blood:	n/a	chr7:97910803-97910812 chr7:97910851-97910860
3	ATF3	chr7:97910813-97911050	H1-hESC	embryonic stem cell:	n/a	chr7:97910851-97910860
4	ATF3	chr7:97910805-97911053	GM12878	blood:	n/a	chr7:97910851-97910860
5	ATF3	chr7:97910823-97911057	HepG2	liver:	n/a	chr7:97910851-97910860
6	ATF3	chr7:97910828-97910981	GM12878	blood:	n/a	chr7:97910851-97910860
7	BACH1	chr7:97910074-97910547	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr7:97910147-97911105	HepG2	liver:	n/a	chr7:97910794-97910810 chr7:97910241-97910257 chr7:97910487-97910503 chr7:97910791-97910807 chr7:97910825-97910841
9	BHLHE40	chr7:97911359-97911360	K562	blood:	n/a	n/a
10	BHLHE40	chr7:97910158-97910542	K562	blood:	n/a	chr7:97910241-97910257 chr7:97910487-97910503
11	BHLHE40	chr7:97910772-97911094	K562	blood:	n/a	chr7:97910794-97910810 chr7:97910791-97910807 chr7:97910825-97910841
12	BHLHE40	chr7:97911312-97911512	GM12878	blood:	n/a	chr7:97911380-97911396
13	BHLHE40	chr7:97910134-97911092	GM12878	blood:	n/a	chr7:97910794-97910810 chr7:97910241-97910257 chr7:97910487-97910503 chr7:97910791-97910807 chr7:97910825-97910841
14	BRCA1	chr7:97912561-97912921	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr7:97910275-97910414	H1-hESC	embryonic stem cell:	n/a	n/a
16	CCNT2	chr7:97910215-97911118	K562	blood:	n/a	chr7:97910598-97910607
17	CEBPB	chr7:97912471-97912761	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:97909729-97910198	H1-hESC	embryonic stem cell:	n/a	chr7:97909864-97909875 chr7:97910160-97910173
19	CEBPB	chr7:97909738-97910630	Hela-S3	cervix:	n/a	chr7:97909864-97909875 chr7:97910160-97910173
20	CEBPB	chr7:97910128-97910155	K562	blood:	n/a	n/a
21	CEBPB	chr7:97909733-97910227	HepG2	liver:	n/a	chr7:97909864-97909875 chr7:97910160-97910173
22	CEBPD	chr7:97910342-97910580	HepG2	liver:	n/a	n/a
23	CEBPD	chr7:97910203-97910784	HepG2	liver:	n/a	n/a
24	CEBPD	chr7:97910808-97911119	HepG2	liver:	n/a	n/a
25	CHD1	chr7:97911400-97911929	GM12878	blood:	n/a	n/a
26	CHD1	chr7:97910882-97912849	IMR90	lung:	n/a	n/a
27	CHD2	chr7:97911874-97912074	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr7:97910693-97910733	K562	blood:	n/a	n/a
29	CHD2	chr7:97910284-97911074	Hela-S3	cervix:	n/a	chr7:97910804-97910814
30	CHD2	chr7:97910393-97910697	GM12878	blood:	n/a	n/a
31	CHD2	chr7:97910151-97910799	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr7:97911462-97911659	GM12878	blood:	n/a	n/a
33	CHD2	chr7:97911727-97911982	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr7:97911406-97911534	HepG2	liver:	n/a	n/a
35	CHD2	chr7:97911395-97911479	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr7:97910367-97910826	HepG2	liver:	n/a	chr7:97910804-97910814
37	CREB1	chr7:97910380-97910835	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr7:97911402-97911798	A549	lung:	n/a	n/a
39	CREB1	chr7:97910280-97910719	A549	lung:	n/a	n/a
40	CTCF	chr7:97910520-97910670	GM12878	blood:	n/a	n/a
41	CTCF	chr7:97910560-97910710	HMEC	breast:	n/a	n/a
42	CTCF	chr7:97910540-97910690	GM12874	blood:	n/a	n/a
43	CTCF	chr7:97910430-97910581	K562	blood:	n/a	n/a
44	CTCF	chr7:97910500-97910650	GM06990	blood:	n/a	n/a
45	CTCF	chr7:97910580-97910730	AG09309	skin:	n/a	n/a
46	CTCF	chr7:97910520-97910670	HRE	kidney:	n/a	n/a
47	CTCF	chr7:97910600-97910750	GM06990	blood:	n/a	n/a
48	CTCF	chr7:97910580-97910730	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr7:97910280-97910430	GM06990	blood:	n/a	chr7:97910294-97910303 chr7:97910291-97910309
50	CTCF	chr7:97910560-97910710	HVMF	connective:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97910728-97910778	IMR90	lung:	fetal
2	chr7:97910870-97910920	HRE	kidney:	n/a
3	chr7:97910728-97910778	IMR90	lung:	fetal
4	chr7:97910870-97910920	HRE	kidney:	n/a
5	chr7:97910728-97910778	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:97910728-97910778	NB4	blood:	n/a
7	chr7:97911938-97911988	RPTEC	kidney:	n/a
8	chr7:97911390-97911440	HEEpiC	esophagus:	n/a
9	chr7:97910392-97910442	RPTEC	kidney:	n/a
10	chr7:97910392-97910442	HAEpiC	amniotic membrane:	n/a
11	chr7:97911512-97911562	H1-hESC	embryonic stem cell:	embryo
12	chr7:97910571-97910621	NB4	blood:	n/a
13	chr7:97910856-97910906	NHDF-neo	bronchial:	n/a
14	chr7:97910856-97910906	HUVEC	blood vessel:	n/a
15	chr7:97910870-97910920	HIPEpiC	eye:	n/a
16	chr7:97910856-97910906	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:97911512-97911562	ProgFib	skin:	n/a
18	chr7:97910878-97910928	HAEpiC	amniotic membrane:	n/a
19	chr7:97910392-97910442	HCPEpiC	choroid plexus:	n/a
20	chr7:97910728-97910778	AG10803	skin:	n/a
21	chr7:97910884-97910934	HMEC	breast:	n/a
22	chr7:97910870-97910920	LNCaP	prostate:	n/a
23	chr7:97911390-97911440	ProgFib	skin:	n/a
24	chr7:97910884-97910934	AG10803	skin:	n/a
25	chr7:97911512-97911562	HCPEpiC	choroid plexus:	n/a
26	chr7:97910728-97910778	SK-N-SH	brain:	n/a
27	chr7:97911390-97911440	Jurkat	blood:	n/a
28	chr7:97911938-97911988	HAEpiC	amniotic membrane:	n/a
29	chr7:97910571-97910621	HAEpiC	amniotic membrane:	n/a
30	chr7:97911938-97911988	HRCEpiC	kidney:	n/a
31	chr7:97911390-97911440	NH-A	brain:	n/a
32	chr7:97911512-97911562	HMEC	breast:	n/a
33	chr7:97910856-97910906	BJ	skin:	n/a
34	chr7:97910878-97910928	ovcar-3	ovarian:	n/a
35	chr7:97910808-97910858	RPTEC	kidney:	n/a
36	chr7:97911938-97911988	HNPCEpiC	eye:	n/a
37	chr7:97910884-97910934	MCF10A-Er-Src	breast:	n/a
38	chr7:97910728-97910778	Hela-S3	cervix:	n/a
39	chr7:97910571-97910621	GM12878	blood:	n/a
40	chr7:97910728-97910778	HepG2	liver:	n/a
41	chr7:97910884-97910934	HCF	heart:	n/a
42	chr7:97910884-97910934	PrEC	prostate:	n/a
43	chr7:97910884-97910934	HNPCEpiC	eye:	n/a
44	chr7:97912149-97912199	SK-N-SH_RA	brain:	n/a
45	chr7:97910808-97910858	NH-A	brain:	n/a
46	chr7:97910870-97910920	Hepatocyte	liver:	n/a
47	chr7:97910856-97910906	U87	brain:	n/a
48	chr7:97911390-97911440	HRE	kidney:	n/a
49	chr7:97910884-97910934	HEEpiC	esophagus:	n/a
50	chr7:97911938-97911988	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:137673487..137674011-chr7:97910467..97911354,2	HCT-116	colon:
2	chr7:97880657..97883457-chr7:97908974..97910800,2	MCF-7	breast:
3	chr7:97880609..97882891-chr7:97909884..97913133,3	MCF-7	breast:
4	chr7:97863932..97867672-chr7:97911936..97914933,4	K562	blood:
5	chr7:97907436..97910241-chr7:97949953..97951454,2	MCF-7	breast:
6	chr7:97900433..97904239-chr7:97908509..97910838,3	K562	blood:

Variant related genes	Relation type
BRI3	TF binding region
BRI3	CpG island
ENSG00000120709	chromatin interactions
ENSG00000164713	chromatin interactions
ENSG00000205356	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529912228	chr7:97910056-97910057	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs546624164	chr7:97910084-97910085	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs141587986	chr7:97910105-97910106	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535514397	chr7:97910106-97910107	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs545896820	chr7:97910109-97910110	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs557301389	chr7:97910143-97910144	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs377473885	chr7:97910155-97910156	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs569029083	chr7:97910209-97910210	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs539511523	chr7:97910263-97910264	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs557937639	chr7:97910264-97910265	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs573052310	chr7:97910277-97910278	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs540814553	chr7:97910318-97910319	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs147527442	chr7:97910327-97910328	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs548039209	chr7:97910341-97910342	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs574255727	chr7:97910350-97910351	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs367558899	chr7:97910361-97910362	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs370224881	chr7:97910377-97910378	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs181274586	chr7:97910453-97910454	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs563241787	chr7:97910454-97910455	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs386716019	chr7:97910488-97910489	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs12113285	chr7:97910489-97910490	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564168995	chr7:97910508-97910509	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs558096111	chr7:97910574-97910575	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs528313875	chr7:97910593-97910594	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs12113294	chr7:97910637-97910638	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs561862171	chr7:97910656-97910657	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs557689930	chr7:97910800-97910801	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs113008721	chr7:97910866-97910867	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs187366195	chr7:97910938-97910939	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs529158359	chr7:97910975-97910976	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs562067767	chr7:97911020-97911021	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs370291662	chr7:97911242-97911243	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs568868731	chr7:97911273-97911274	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs539547405	chr7:97911316-97911317	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs370549051	chr7:97911319-97911320	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs374997704	chr7:97911322-97911323	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs533868765	chr7:97911329-97911330	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs375180244	chr7:97911336-97911337	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs566942684	chr7:97911343-97911344	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs575288976	chr7:97911358-97911359	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs140174552	chr7:97911387-97911388	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs555903067	chr7:97911428-97911429	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs574270838	chr7:97911436-97911437	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs538490378	chr7:97911475-97911476	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs73391022	chr7:97911486-97911487	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs113937437	chr7:97911498-97911499	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs575359321	chr7:97911503-97911504	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs558628070	chr7:97911509-97911510	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs545805485	chr7:97911556-97911557	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs58983614	chr7:97911561-97911562	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD

Chromatin state (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97907800-97910200	Enhancers	Stomach Mucosa	stomach
2	chr7:97908400-97910200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:97908800-97910200	Weak transcription	Lung	lung
4	chr7:97909400-97910200	Weak transcription	Gastric	stomach
5	chr7:97909600-97910400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr7:97909800-97910200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:97909800-97910200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr7:97909800-97910200	Enhancers	Small Intestine	intestine
9	chr7:97909800-97910200	Enhancers	Spleen	Spleen
10	chr7:97909800-97910200	Flanking Active TSS	HepG2	liver
11	chr7:97909800-97910400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
12	chr7:97909800-97910400	Flanking Active TSS	Primary B cells from cord blood	blood
13	chr7:97909800-97910400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
14	chr7:97909800-97910400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
15	chr7:97909800-97910400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr7:97909800-97910400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:97909800-97910400	Flanking Active TSS	Brain Hippocampus Middle	brain
18	chr7:97909800-97910400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:97909800-97910400	Flanking Active TSS	Fetal Intestine Large	intestine
20	chr7:97909800-97910400	Flanking Active TSS	Fetal Intestine Small	intestine
21	chr7:97909800-97910400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
22	chr7:97909800-97910400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr7:97909800-97910600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr7:97909800-97910600	Flanking Active TSS	Primary hematopoietic stem cells	blood
25	chr7:97909800-97910600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr7:97909800-97910600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr7:97909800-97910600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:97909800-97910600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:97909800-97910600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr7:97909800-97910600	Flanking Active TSS	Duodenum Mucosa	Duodenum
31	chr7:97909800-97910600	Flanking Active TSS	Placenta	Placenta
32	chr7:97909800-97910600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
33	chr7:97909800-97910600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
34	chr7:97909800-97911400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr7:97909800-97911600	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr7:97909800-97911600	Active TSS	Primary T cells from cord blood	blood
37	chr7:97909800-97911800	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr7:97909800-97911800	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr7:97909800-97911800	Active TSS	Fetal Brain Female	brain
40	chr7:97909800-97911800	Active TSS	Rectal Smooth Muscle	rectum
41	chr7:97909800-97912000	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr7:97909800-97912000	Active TSS	Brain Germinal Matrix	brain
43	chr7:97909800-97912000	Active TSS	Colon Smooth Muscle	Colon
44	chr7:97909800-97914200	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr7:97910000-97910200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
46	chr7:97910000-97910200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:97910000-97910200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:97910000-97910200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
49	chr7:97910000-97910200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr7:97910000-97910200	Flanking Active TSS	Brain Anterior Caudate	brain

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