Variant report

Variant	nsv889062
Chromosome Location	chr7:112920080-113138047
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	chr7:113100171-113100369	HepG2	liver:	n/a	n/a
2	ATF1	chr7:112989582-112989666	K562	blood:	n/a	n/a
3	ATF1	chr7:112946391-112946665	K562	blood:	n/a	n/a
4	ATF1	chr7:113011968-113011971	K562	blood:	n/a	n/a
5	ATF1	chr7:112921615-112921625	K562	blood:	n/a	n/a
6	ATF1	chr7:112929247-112929556	K562	blood:	n/a	n/a
7	BCLAF1	chr7:113061693-113062163	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:112942154-112942280	K562	blood:	n/a	n/a
9	BHLHE40	chr7:112971718-112971776	K562	blood:	n/a	n/a
10	BHLHE40	chr7:112957742-112957966	K562	blood:	n/a	chr7:112957843-112957864 chr7:112957849-112957858 chr7:112957849-112957858 chr7:112957848-112957857 chr7:112957847-112957860 chr7:112957850-112957859
11	BHLHE40	chr7:113061606-113062157	K562	blood:	n/a	chr7:113061662-113061675 chr7:113061931-113061947
12	BRCA1	chr7:113035535-113035595	HepG2	liver:	n/a	n/a
13	CBX3	chr7:113061624-113062128	K562	blood:	n/a	n/a
14	CEBPB	chr7:112979137-112979342	MCF-7	breast:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
15	CEBPB	chr7:113123365-113123597	HepG2	liver:	n/a	chr7:113123443-113123456 chr7:113123443-113123454
16	CEBPB	chr7:112929290-112929518	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:113034880-113035251	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:112997394-112997628	HepG2	liver:	n/a	chr7:112997485-112997496
19	CEBPB	chr7:113017407-113017460	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:113100782-113101065	IMR90	lung:	n/a	chr7:113100926-113100937
21	CEBPB	chr7:112979078-112979370	HepG2	liver:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
22	CEBPB	chr7:112997353-112997549	K562	blood:	n/a	chr7:112997485-112997496
23	CEBPB	chr7:113015119-113015397	K562	blood:	n/a	n/a
24	CEBPB	chr7:113100794-113101095	K562	blood:	n/a	chr7:113100926-113100937
25	CEBPB	chr7:112946416-112946690	K562	blood:	n/a	n/a
26	CEBPB	chr7:112929225-112929501	K562	blood:	n/a	n/a
27	CEBPB	chr7:113100777-113101040	A549	lung:	n/a	chr7:113100926-113100937
28	CEBPB	chr7:112979132-112979407	K562	blood:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
29	CEBPB	chr7:112929188-112929394	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:112979171-112979371	A549	lung:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
31	CEBPB	chr7:113100776-113101095	HepG2	liver:	n/a	chr7:113100926-113100937
32	CEBPB	chr7:112923333-112923623	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:112929967-112930238	MCF-7	breast:	n/a	n/a
34	CEBPB	chr7:112975731-112975761	IMR90	lung:	n/a	chr7:112975743-112975754
35	CEBPB	chr7:113033846-113034160	HepG2	liver:	n/a	chr7:113033966-113033977 chr7:113034007-113034018 chr7:113033964-113033977
36	CEBPB	chr7:112927318-112927616	K562	blood:	n/a	n/a
37	CEBPB	chr7:112975641-112975770	A549	lung:	n/a	chr7:112975743-112975754
38	CEBPB	chr7:112925506-112925869	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:112975635-112975796	HepG2	liver:	n/a	chr7:112975743-112975754
40	CEBPB	chr7:113084552-113084769	HepG2	liver:	n/a	chr7:113084695-113084706
41	CEBPB	chr7:113056258-113056371	K562	blood:	n/a	n/a
42	CEBPB	chr7:112979104-112979378	IMR90	lung:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
43	CEBPD	chr7:112946369-112946800	K562	blood:	n/a	n/a
44	CHD1	chr7:113044042-113044205	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr7:112971573-112971821	K562	blood:	n/a	n/a
46	CHD2	chr7:112971477-112971766	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr7:113044440-113044590	HAc	cerebellar:	n/a	chr7:113044475-113044493 chr7:113044480-113044490 chr7:113044478-113044491 chr7:113044477-113044498 chr7:113044476-113044492 chr7:113044478-113044487
48	CTCF	chr7:113061422-113062356	A549	lung:	n/a	chr7:113061970-113061988 chr7:113061972-113061985 chr7:113061965-113061986 chr7:113061935-113061948 chr7:113061933-113061951 chr7:113061940-113061948
49	CTCF	chr7:113044400-113044550	HCT-116	colon:	n/a	chr7:113044475-113044493 chr7:113044480-113044490 chr7:113044478-113044491 chr7:113044477-113044498 chr7:113044476-113044492 chr7:113044478-113044487
50	CTCF	chr7:113055716-113055797	Gliobla	brain:	n/a	chr7:113055718-113055731

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:113090002-113090052	AG04450	lung:	fetal
2	chr7:113090002-113090052	GM12878	blood:	n/a
3	chr7:113091000-113091050	SKMC	muscle:	n/a
4	chr7:113011963-113012013	NB4	blood:	n/a
5	chr7:113011963-113012013	SK-N-MC	brain:	n/a
6	chr7:113091000-113091050	BJ	skin:	n/a
7	chr7:113090002-113090052	H1-hESC	embryonic stem cell:	embryo
8	chr7:113034122-113034172	HCPEpiC	choroid plexus:	n/a
9	chr7:113091000-113091050	ProgFib	skin:	n/a
10	chr7:113090002-113090052	ECC-1	luminal epithelium:	n/a
11	chr7:113034122-113034172	AG04450	lung:	fetal
12	chr7:113090002-113090052	NH-A	brain:	n/a
13	chr7:113091000-113091050	NH-A	brain:	n/a
14	chr7:113090002-113090052	MCF10A-Er-Src	breast:	n/a
15	chr7:113034122-113034172	LNCaP	prostate:	n/a
16	chr7:113011963-113012013	HRE	kidney:	n/a
17	chr7:113090002-113090052	HUVEC	blood vessel:	n/a
18	chr7:113034122-113034172	SK-N-MC	brain:	n/a
19	chr7:113011963-113012013	PFSK-1	brain:	n/a
20	chr7:113090002-113090052	SAEC	small airway:	n/a
21	chr7:113091000-113091050	A549	lung:	n/a
22	chr7:113034122-113034172	HUVEC	blood vessel:	n/a
23	chr7:113090002-113090052	SK-N-SH	brain:	n/a
24	chr7:113091000-113091050	AG10803	skin:	n/a
25	chr7:113034122-113034172	CMK	blood:	n/a
26	chr7:113011963-113012013	HCPEpiC	choroid plexus:	n/a
27	chr7:113011963-113012013	NH-A	brain:	n/a
28	chr7:113034122-113034172	IMR90	lung:	fetal
29	chr7:113091000-113091050	HCT-116	colon:	n/a
30	chr7:113011963-113012013	HCM	heart:	n/a
31	chr7:113034122-113034172	Hepatocyte	liver:	n/a
32	chr7:113034122-113034172	HCM	heart:	n/a
33	chr7:113090002-113090052	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:113090002-113090052	K562	blood:	n/a
35	chr7:113091000-113091050	T-47D	breast:	n/a
36	chr7:113011963-113012013	PANC-1	pancreas:	n/a
37	chr7:113090002-113090052	CMK	blood:	n/a
38	chr7:113011963-113012013	HUVEC	blood vessel:	n/a
39	chr7:113090002-113090052	HCM	heart:	n/a
40	chr7:113034122-113034172	ProgFib	skin:	n/a
41	chr7:113011963-113012013	Hela-S3	cervix:	n/a
42	chr7:113090002-113090052	HNPCEpiC	eye:	n/a
43	chr7:113090002-113090052	HEEpiC	esophagus:	n/a
44	chr7:113091000-113091050	AG04449	skin:	fetal
45	chr7:113091000-113091050	LNCaP	prostate:	n/a
46	chr7:113091000-113091050	Hela-S3	cervix:	n/a
47	chr7:113091000-113091050	PANC-1	pancreas:	n/a
48	chr7:113011963-113012013	NT2-D1	testis:	n/a
49	chr7:113034122-113034172	HMEC	breast:	n/a
50	chr7:113090002-113090052	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:112903603..112905709-chr7:112919936..112922248,2	K562	blood:
2	chr7:112758684..112760391-chr7:112965987..112967563,2	K562	blood:
3	chr7:113001622..113003808-chr7:113017179..113018966,2	MCF-7	breast:
4	chr7:113101413..113104143-chr7:113123291..113125163,2	MCF-7	breast:
5	chr7:112955793..112957716-chr7:112966619..112968256,2	K562	blood:
6	chr7:112919737..112922659-chr7:112922848..112924621,2	MCF-7	breast:
7	chr7:112914755..112918139-chr7:112919654..112923102,3	K562	blood:
8	chr7:112190294..112191180-chr7:113061506..113062330,4	MCF-7	breast:
9	chr7:113043772..113046684-chr7:113053716..113055424,2	MCF-7	breast:
10	chr7:112949710..112952424-chr7:112954209..112957100,2	K562	blood:
11	chr7:112919908..112922049-chr7:112922331..112926205,3	MCF-7	breast:
12	chr7:112919737..112922659-chr7:112922848..112924621,2	MCF-7	breast:
13	chr7:113100189..113102215-chr7:113103727..113106100,2	K562	blood:
14	chr7:113026289..113028138-chr7:113029115..113030912,2	K562	blood:
15	chr7:112986796..112990552-chr7:112993911..112996520,3	MCF-7	breast:
16	chr7:112089237..112091482-chr7:112936057..112938859,2	MCF-7	breast:
17	chr7:112799910..112800953-chr7:113061499..113062556,5	MCF-7	breast:
18	chr7:113053644..113055850-chr7:113060152..113062983,2	MCF-7	breast:
19	chr7:113030617..113032266-chr7:113032276..113034462,2	K562	blood:
20	chr7:99433750..99434429-chr7:113008535..113009149,2	MCF-7	breast:
21	chr7:112799588..112800619-chr7:113061470..113062718,9	MCF-7	breast:
22	chr7:113043772..113046684-chr7:113053716..113055424,2	MCF-7	breast:
23	chr7:112809313..112813953-chr7:112918870..112922668,5	MCF-7	breast:
24	chr7:112940051..112941689-chr7:112965313..112967695,2	K562	blood:
25	chr7:113101413..113104143-chr7:113123291..113125163,2	MCF-7	breast:
26	chr7:113042048..113044438-chr7:113046056..113047809,2	K562	blood:
27	chr7:112757111..112758761-chr7:112957701..112959232,2	K562	blood:
28	chr7:113044065..113044754-chr7:113061519..113062155,3	MCF-7	breast:
29	chr7:113011064..113013655-chr7:113032102..113033697,2	K562	blood:
30	chr7:112655256..112655797-chr7:112929374..112930128,2	MCF-7	breast:
31	chr7:112509091..112509840-chr7:113061486..113062019,3	MCF-7	breast:
32	chr7:113033970..113036356-chr7:113044345..113046971,2	K562	blood:
33	chr7:113044065..113044754-chr7:113061519..113062155,3	MCF-7	breast:
34	chr7:112919539..112924993-chr7:112925229..112928766,5	MCF-7	breast:
35	chr7:112758299..112760850-chr7:113043245..113045081,2	K562	blood:
36	chr7:112950198..112952565-chr7:112958215..112960663,2	MCF-7	breast:
37	chr7:113061631..113062403-chr7:113350437..113351122,2	MCF-7	breast:
38	chr7:113086419..113088488-chr7:113090237..113092945,2	K562	blood:
39	chr7:112953049..112955491-chr7:112958920..112960893,2	K562	blood:
40	chr7:113026289..113028138-chr7:113029115..113030912,2	K562	blood:
41	chr7:112965647..112967560-chr7:112969669..112971397,2	K562	blood:
42	chr7:112654983..112656027-chr7:113061405..113062486,9	MCF-7	breast:
43	chr7:113001622..113003808-chr7:113017179..113018966,2	MCF-7	breast:
44	chr7:113011064..113013655-chr7:113032102..113033697,2	K562	blood:
45	chr7:113030617..113032266-chr7:113032276..113034462,2	K562	blood:
46	chr7:113042011..113045853-chr7:113047811..113051782,4	MCF-7	breast:
47	chr7:112986796..112990552-chr7:112993911..112996520,3	MCF-7	breast:
48	chr7:112799464..112800464-chr7:113061264..113062480,6	K562	blood:
49	chr7:112953049..112955491-chr7:112958920..112960893,2	K562	blood:
50	chr7:113028637..113030163-chr7:113052999..113055912,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073346.2.1-1	chr7:113137638-113137756	XLOC_006565
2	lnc-AC073346.2.1-1	chr7:113134743-113134798	XLOC_006565
3	lnc-AC073348.1-5	chr7:113055744-113056377	NONHSAT122817
4	lnc-AC073348.1-4	chr7:113109789-113110137	NONHSAT122818
5	lnc-AC073348.1-4	chr7:113117164-113124124	NONHSAT122818

Variant related genes	Relation type
ENSG00000270997	TF binding region
ENSG00000236294	TF binding region
ENSG00000270997	CpG island
ENSG00000236294	CpG island
ENSG00000164603	chromatin interactions
ENSG00000214194	chromatin interactions
ENSG00000270997	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000236294	chromatin interactions

Extended variants
information (count: 4447 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:4447 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2140636	chr7:112920080-112920081	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535277754	chr7:112920138-112920139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78698981	chr7:112920140-112920141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546088599	chr7:112920203-112920204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565013551	chr7:112920209-112920210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576062478	chr7:112920269-112920270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373488410	chr7:112920298-112920299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545478287	chr7:112920303-112920304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556163171	chr7:112920316-112920317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149728641	chr7:112920324-112920325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144485336	chr7:112920331-112920332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559861287	chr7:112920345-112920346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533357325	chr7:112920367-112920368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576899969	chr7:112920372-112920373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191488800	chr7:112920396-112920397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537038307	chr7:112920412-112920413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182516346	chr7:112920473-112920474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76771399	chr7:112920510-112920511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567632199	chr7:112920561-112920562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535091884	chr7:112920689-112920690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73430409	chr7:112920699-112920700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572166399	chr7:112920754-112920755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539649565	chr7:112920805-112920806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558084342	chr7:112920819-112920820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576448590	chr7:112920826-112920827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs118079674	chr7:112920834-112920835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561693778	chr7:112920870-112920871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148439346	chr7:112920886-112920887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541080307	chr7:112920894-112920895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188419739	chr7:112920964-112920965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533345713	chr7:112920974-112920975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377211330	chr7:112921012-112921013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114365337	chr7:112921041-112921042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541206571	chr7:112921061-112921062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531137830	chr7:112921071-112921072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541554135	chr7:112921081-112921082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549434758	chr7:112921101-112921102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs578043944	chr7:112921111-112921112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199687395	chr7:112921241-112921242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375175279	chr7:112921243-112921244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369554666	chr7:112921244-112921245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200574876	chr7:112921246-112921247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200184623	chr7:112921248-112921249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534720084	chr7:112921270-112921271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192251908	chr7:112921278-112921279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149016116	chr7:112921279-112921280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547027295	chr7:112921280-112921281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184570952	chr7:112921372-112921373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539636494	chr7:112921409-112921410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202002925	chr7:112921412-112921413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112918600-112921400	Enhancers	Fetal Heart	heart
2	chr7:112919600-112923200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr7:112921400-112923400	Weak transcription	Fetal Heart	heart
4	chr7:112923200-112923600	Enhancers	Placenta Amnion	Placenta Amnion
5	chr7:112923400-112924200	Enhancers	Fetal Heart	heart
6	chr7:112923600-112924400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr7:112923600-112926600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr7:112923800-112924200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:112924200-112924400	Enhancers	Osteobl	bone
10	chr7:112924200-112924600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr7:112924200-112924800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:112924400-112925400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr7:112924400-112925400	Weak transcription	Osteobl	bone
14	chr7:112924600-112926000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:112924800-112925200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:112925200-112926000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:112925400-112926000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr7:112925400-112926200	Enhancers	Osteobl	bone
19	chr7:112929400-112929600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:112931200-112931800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:112931200-112932000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:112931400-112931600	Enhancers	Esophagus	oesophagus
23	chr7:112931800-112932000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:112932000-112932400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:112932200-112932400	Enhancers	Esophagus	oesophagus
26	chr7:112932200-112932600	Enhancers	Adipose Nuclei	Adipose
27	chr7:112932200-112932800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:112932400-112932600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:112932600-112934400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:112934400-112935200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:112935000-112935600	ZNF genes & repeats	Esophagus	oesophagus
32	chr7:112946200-112946800	Active TSS	K562	blood
33	chr7:112946800-112947400	Weak transcription	K562	blood
34	chr7:112947400-112948200	Enhancers	K562	blood
35	chr7:112948400-112948800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:112951800-112952000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:112952000-112952400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:112952000-112952400	Enhancers	Adipose Nuclei	Adipose
39	chr7:112952000-112953200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:112952400-112952800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:112952400-112954800	Weak transcription	Adipose Nuclei	Adipose
42	chr7:112952800-112954200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:112953200-112954600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr7:112954200-112955000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:112954400-112955200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr7:112954400-112955400	Enhancers	Fetal Lung	lung
47	chr7:112954600-112955000	Enhancers	Colon Smooth Muscle	Colon
48	chr7:112954600-112955200	Enhancers	Fetal Heart	heart
49	chr7:112954600-112955600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:112954800-112955200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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