Variant report

Variant	nsv889245
Chromosome Location	chr7:139599229-139657221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:850)
CpG islands
(count:184)
Chromatin interactive
region (count:94)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:139615674-139616592	K562	blood:	n/a	n/a
2	ARID3A	chr7:139608676-139608997	K562	blood:	n/a	n/a
3	ARID3A	chr7:139650818-139651229	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:139614203-139614407	K562	blood:	n/a	n/a
5	ARID3A	chr7:139648468-139648738	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:139618414-139619062	K562	blood:	n/a	n/a
7	ATF1	chr7:139630499-139630693	K562	blood:	n/a	n/a
8	ATF1	chr7:139615844-139616567	K562	blood:	n/a	n/a
9	ATF1	chr7:139608654-139608815	K562	blood:	n/a	n/a
10	ATF1	chr7:139636644-139636982	K562	blood:	n/a	n/a
11	ATF1	chr7:139640816-139640973	K562	blood:	n/a	n/a
12	ATF2	chr7:139615901-139617267	GM12878	blood:	n/a	n/a
13	ATF2	chr7:139616151-139616768	GM12878	blood:	n/a	n/a
14	ATF3	chr7:139615990-139616554	K562	blood:	n/a	n/a
15	ATF3	chr7:139615667-139616639	K562	blood:	n/a	n/a
16	ATF3	chr7:139636620-139636936	K562	blood:	n/a	n/a
17	ATF3	chr7:139636581-139636986	K562	blood:	n/a	n/a
18	BACH1	chr7:139615502-139616530	K562	blood:	n/a	chr7:139616415-139616429 chr7:139615978-139615992
19	BACH1	chr7:139649358-139649362	K562	blood:	n/a	n/a
20	BACH1	chr7:139614016-139614395	H1-hESC	embryonic stem cell:	n/a	chr7:139614206-139614220
21	BACH1	chr7:139618454-139618638	K562	blood:	n/a	n/a
22	BACH1	chr7:139613432-139613679	K562	blood:	n/a	n/a
23	BACH1	chr7:139611117-139611163	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:139612405-139612408	K562	blood:	n/a	n/a
25	BACH1	chr7:139628328-139628524	K562	blood:	n/a	n/a
26	BACH1	chr7:139615841-139616094	H1-hESC	embryonic stem cell:	n/a	chr7:139615978-139615992
27	BACH1	chr7:139613964-139614985	K562	blood:	n/a	chr7:139614206-139614220
28	BATF	chr7:139616718-139617199	GM12878	blood:	n/a	n/a
29	BATF	chr7:139616268-139616609	GM12878	blood:	n/a	chr7:139616456-139616467 chr7:139616414-139616425
30	BATF	chr7:139616122-139616714	GM12878	blood:	n/a	chr7:139616456-139616467 chr7:139616414-139616425
31	BCL11A	chr7:139616194-139616712	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:139599403-139599636	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:139616256-139616547	GM12878	blood:	n/a	n/a
34	BCL3	chr7:139616073-139616705	GM12878	blood:	n/a	n/a
35	BCL3	chr7:139615568-139616674	A549	lung:	n/a	chr7:139616054-139616062
36	BCLAF1	chr7:139616041-139617388	GM12878	blood:	n/a	chr7:139616054-139616062
37	BCLAF1	chr7:139616736-139617218	GM12878	blood:	n/a	n/a
38	BCLAF1	chr7:139616043-139616726	GM12878	blood:	n/a	chr7:139616054-139616062
39	BHLHE40	chr7:139615410-139615531	K562	blood:	n/a	n/a
40	BHLHE40	chr7:139616227-139617182	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:139615910-139616581	K562	blood:	n/a	n/a
42	BHLHE40	chr7:139636714-139636914	K562	blood:	n/a	n/a
43	BHLHE40	chr7:139648365-139648711	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:139618060-139618653	K562	blood:	n/a	chr7:139618115-139618124 chr7:139618116-139618125
45	BHLHE40	chr7:139614262-139614465	K562	blood:	n/a	n/a
46	CBX3	chr7:139636456-139637095	K562	blood:	n/a	n/a
47	CBX3	chr7:139608454-139610139	K562	blood:	n/a	n/a
48	CBX3	chr7:139614018-139617208	K562	blood:	n/a	n/a
49	CBX3	chr7:139618164-139618861	K562	blood:	n/a	n/a
50	CBX3	chr7:139614184-139614680	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:139642893-139642943	HL-60	blood:	n/a
2	chr7:139642893-139642943	HL-60	blood:	n/a
3	chr7:139637446-139637496	BE2_C	brain:	n/a
4	chr7:139614808-139614858	HCM	heart:	n/a
5	chr7:139637446-139637496	LNCaP	prostate:	n/a
6	chr7:139637446-139637496	BJ	skin:	n/a
7	chr7:139642893-139642943	SAEC	small airway:	n/a
8	chr7:139642893-139642943	HCM	heart:	n/a
9	chr7:139614808-139614858	AoSMC	blood vessel:	n/a
10	chr7:139614808-139614858	U87	brain:	n/a
11	chr7:139637446-139637496	MCF-7	breast:	n/a
12	chr7:139614808-139614858	HEK293	kidney:	embryo
13	chr7:139642893-139642943	ProgFib	skin:	n/a
14	chr7:139642893-139642943	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:139642893-139642943	U87	brain:	n/a
16	chr7:139614808-139614858	Hela-S3	cervix:	n/a
17	chr7:139614808-139614858	HEEpiC	esophagus:	n/a
18	chr7:139642893-139642943	SK-N-MC	brain:	n/a
19	chr7:139614808-139614858	HRPEpiC	eye:	n/a
20	chr7:139614808-139614858	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:139614808-139614858	NHDF-neo	bronchial:	n/a
22	chr7:139642893-139642943	ECC-1	luminal epithelium:	n/a
23	chr7:139614808-139614858	NT2-D1	testis:	n/a
24	chr7:139642893-139642943	CMK	blood:	n/a
25	chr7:139637446-139637496	NHBE	bronchial:	n/a
26	chr7:139637446-139637496	HRCEpiC	kidney:	n/a
27	chr7:139642893-139642943	NB4	blood:	n/a
28	chr7:139614808-139614858	SK-N-MC	brain:	n/a
29	chr7:139642893-139642943	PANC-1	pancreas:	n/a
30	chr7:139637446-139637496	SKMC	muscle:	n/a
31	chr7:139637446-139637496	T-47D	breast:	n/a
32	chr7:139637446-139637496	GM19239	blood:	n/a
33	chr7:139637446-139637496	GM12892	blood:	n/a
34	chr7:139637446-139637496	GM12878	blood:	n/a
35	chr7:139614808-139614858	Caco-2	colon:	n/a
36	chr7:139614808-139614858	AG09319	gingival:	n/a
37	chr7:139642893-139642943	SK-N-SH	brain:	n/a
38	chr7:139614808-139614858	SKMC	muscle:	n/a
39	chr7:139614808-139614858	GM12891	blood:	n/a
40	chr7:139642893-139642943	Hela-S3	cervix:	n/a
41	chr7:139614808-139614858	HRE	kidney:	n/a
42	chr7:139642893-139642943	SK-N-SH_RA	brain:	n/a
43	chr7:139637446-139637496	SAEC	small airway:	n/a
44	chr7:139642893-139642943	AoSMC	blood vessel:	n/a
45	chr7:139637446-139637496	HMEC	breast:	n/a
46	chr7:139637446-139637496	RPTEC	kidney:	n/a
47	chr7:139642893-139642943	HAEpiC	amniotic membrane:	n/a
48	chr7:139614808-139614858	HAEpiC	amniotic membrane:	n/a
49	chr7:139614808-139614858	HMEC	breast:	n/a
50	chr7:139637446-139637496	K562	blood:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:139595708..139599443-chr7:139649328..139652268,3	MCF-7	breast:
2	chr7:139650846..139652754-chr7:139657378..139659276,2	MCF-7	breast:
3	chr7:139648168..139649794-chr7:139652428..139654980,2	K562	blood:
4	chr7:139607014..139608551-chr7:139612909..139615880,2	K562	blood:
5	chr7:139617102..139619901-chr7:139650362..139652571,2	K562	blood:
6	chr7:139647807..139650968-chr7:139651691..139656029,5	K562	blood:
7	chr7:139641847..139644053-chr7:139646879..139649393,2	MCF-7	breast:
8	chr7:139636456..139638180-chr7:139647527..139649483,2	K562	blood:
9	chr7:139469062..139470593-chr7:139616161..139618047,2	K562	blood:
10	chr7:139611287..139613050-chr7:139636783..139638353,2	K562	blood:
11	chr7:139584185..139586442-chr7:139614937..139617352,2	K562	blood:
12	chr7:139614974..139617171-chr7:139678956..139681260,2	K562	blood:
13	chr7:139583780..139588622-chr7:139595731..139600740,4	K562	blood:
14	chr7:139619931..139621837-chr7:139655135..139658057,2	K562	blood:
15	chr7:139642819..139644356-chr7:139740604..139743410,2	K562	blood:
16	chr7:139550951..139553349-chr7:139614686..139616321,2	K562	blood:
17	chr7:139586458..139589316-chr7:139614589..139616805,2	K562	blood:
18	chr7:139651749..139653892-chr7:139655715..139657279,2	MCF-7	breast:
19	chr7:139608918..139612096-chr7:139612765..139616269,8	K562	blood:
20	chr7:139614916..139618686-chr7:139627017..139630636,4	K562	blood:
21	chr7:139608918..139612096-chr7:139612765..139616269,8	K562	blood:
22	chr7:139612773..139615272-chr7:139618584..139621625,3	K562	blood:
23	chr7:139612773..139615272-chr7:139618584..139621625,3	K562	blood:
24	chr7:139642517..139644523-chr7:139656724..139658712,2	K562	blood:
25	chr7:139644357..139647303-chr7:139647487..139650390,4	K562	blood:
26	chr7:139597457..139599569-chr7:139609455..139612217,2	K562	blood:
27	chr7:139636566..139639672-chr7:139642737..139644709,4	K562	blood:
28	chr7:139618302..139620555-chr7:139646388..139648923,2	K562	blood:
29	chr7:139605098..139607910-chr7:139614659..139616378,2	K562	blood:
30	chr7:139601541..139604051-chr7:139619127..139620710,2	K562	blood:
31	chr7:139609132..139615823-chr7:139616902..139621625,10	K562	blood:
32	chr7:139599894..139601484-chr7:139605045..139606596,2	K562	blood:
33	chr7:139605098..139607910-chr7:139614659..139616378,2	K562	blood:
34	chr7:139588216..139590014-chr7:139618480..139620084,2	K562	blood:
35	chr7:139614506..139616528-chr7:139619722..139621611,2	MCF-7	breast:
36	chr7:139631371..139634056-chr7:139637713..139640243,2	K562	blood:
37	chr7:139574219..139575833-chr7:139617525..139620392,2	K562	blood:
38	chr7:139619411..139622520-chr7:139671470..139673842,3	K562	blood:
39	chr7:139611287..139613050-chr7:139636783..139638353,2	K562	blood:
40	chr7:139634343..139637163-chr7:139642055..139644058,2	MCF-7	breast:
41	chr7:139607014..139608551-chr7:139612909..139615880,2	K562	blood:
42	chr7:139521931..139523978-chr7:139621670..139623337,2	K562	blood:
43	chr7:139614469..139616397-chr7:139665107..139667475,2	K562	blood:
44	chr7:139635222..139637429-chr7:139651443..139653383,2	MCF-7	breast:
45	chr7:139646007..139647559-chr7:139650550..139653385,2	K562	blood:
46	chr7:139614806..139616915-chr7:139674310..139676178,2	K562	blood:
47	chr7:139476437..139478390-chr7:139635969..139638135,2	K562	blood:
48	chr7:139614916..139618686-chr7:139627017..139630636,4	K562	blood:
49	chr7:139609932..139611578-chr7:139613494..139615788,2	MCF-7	breast:
50	chr7:139616579..139619472-chr7:139620171..139622168,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2L-4	chr7:139646953-139646962	NONHSAT123657
2	lnc-CLEC2L-4	chr7:139639478-139646946	NONHSAT123657

No data

Variant related genes	Relation type
TBXAS1	TF binding region
TBXAS1	CpG island
ENSG00000064393	chromatin interactions
ENSG00000059378	chromatin interactions
ENSG00000059377	chromatin interactions

Extended variants
information (count: 2266 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2266 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8192824	chr7:139599229-139599230	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374145276	chr7:139599249-139599250	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529750791	chr7:139599304-139599305	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548086156	chr7:139599313-139599314	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566670133	chr7:139599379-139599380	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143162313	chr7:139599445-139599446	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376679582	chr7:139599451-139599452	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552483821	chr7:139599494-139599495	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77520365	chr7:139599607-139599608	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs151226717	chr7:139599627-139599628	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190297204	chr7:139599648-139599649	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568465469	chr7:139599656-139599657	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533565376	chr7:139599741-139599742	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181858473	chr7:139599768-139599769	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141518294	chr7:139599772-139599773	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73734141	chr7:139599795-139599796	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555422121	chr7:139599796-139599797	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572292196	chr7:139599804-139599805	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147031294	chr7:139599864-139599865	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558050141	chr7:139599883-139599884	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573256165	chr7:139599896-139599897	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187280998	chr7:139599955-139599956	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562454780	chr7:139599979-139599980	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192111776	chr7:139600094-139600095	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs541898558	chr7:139600104-139600105	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs369179804	chr7:139600193-139600194	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs117840391	chr7:139600208-139600209	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs112439262	chr7:139600221-139600222	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs552366598	chr7:139600272-139600273	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570769483	chr7:139600291-139600292	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs554629616	chr7:139600299-139600300	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs13228722	chr7:139600309-139600310	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs75315730	chr7:139600418-139600419	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs576159905	chr7:139600493-139600494	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs540678872	chr7:139600529-139600530	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs182164977	chr7:139600541-139600542	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs535611244	chr7:139600553-139600554	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs553830767	chr7:139600575-139600576	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs565811125	chr7:139600628-139600629	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs539657080	chr7:139600635-139600636	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs143909088	chr7:139600676-139600677	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs185107091	chr7:139600723-139600724	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs75074215	chr7:139600771-139600772	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs150231557	chr7:139600786-139600787	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs189929939	chr7:139600791-139600792	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs574358781	chr7:139600792-139600793	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs542683535	chr7:139600800-139600801	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs373203211	chr7:139600881-139600882	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs560305026	chr7:139600902-139600903	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs182614681	chr7:139600910-139600911	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:139577000-139612400	Weak transcription	Thymus	Thymus
2	chr7:139592000-139599800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:139593800-139599400	Genic enhancers	Primary monocytes fromperipheralblood	blood
4	chr7:139594200-139600600	Weak transcription	Lung	lung
5	chr7:139594200-139601600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:139594800-139601000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr7:139595200-139600600	Weak transcription	Primary B cells from cord blood	blood
8	chr7:139596400-139600400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr7:139596600-139600000	Genic enhancers	Monocytes-CD14+_RO01746	blood
10	chr7:139597400-139601200	Weak transcription	Gastric	stomach
11	chr7:139597600-139599600	Weak transcription	Fetal Intestine Small	intestine
12	chr7:139598200-139599600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr7:139598200-139600600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr7:139598200-139611400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr7:139598800-139599600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr7:139598800-139599800	Enhancers	GM12878-XiMat	blood
17	chr7:139599000-139600200	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr7:139599200-139600800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:139599200-139612800	Weak transcription	Spleen	Spleen
20	chr7:139599400-139603000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr7:139599600-139599800	Enhancers	Primary B cells from peripheral blood	blood
22	chr7:139599600-139600600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr7:139599800-139600200	Weak transcription	Primary B cells from peripheral blood	blood
24	chr7:139599800-139600200	Strong transcription	Primary hematopoietic stem cells	blood
25	chr7:139600000-139600200	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
26	chr7:139600200-139602200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr7:139600200-139602200	Enhancers	Primary B cells from peripheral blood	blood
28	chr7:139600200-139602200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr7:139600200-139602400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr7:139600400-139602000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:139600600-139601000	Enhancers	Adipose Nuclei	Adipose
32	chr7:139600600-139601000	Enhancers	Lung	lung
33	chr7:139600600-139601600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:139600600-139601800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr7:139600600-139602600	Enhancers	Primary B cells from cord blood	blood
36	chr7:139600600-139605800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr7:139600800-139602000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:139601000-139609600	Weak transcription	Lung	lung
39	chr7:139601400-139601600	Enhancers	Gastric	stomach
40	chr7:139602000-139604200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:139602200-139609800	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr7:139602400-139602800	Genic enhancers	Monocytes-CD14+_RO01746	blood
43	chr7:139602800-139603200	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr7:139603000-139605800	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr7:139603200-139606200	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr7:139604200-139605200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:139604600-139605000	Enhancers	Primary B cells from cord blood	blood
48	chr7:139605200-139607200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:139605800-139607000	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr7:139605800-139607000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood

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