Variant report

Variant	nsv888935
Chromosome Location	chr7:105110990-105193051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1968)
CpG islands
(count:1956)
Chromatin interactive
region (count:139)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1968 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105173865-105174045	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:105141763-105141769	K562	blood:	n/a	n/a
3	ARID3A	chr7:105172230-105172894	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:105128201-105128752	K562	blood:	n/a	n/a
5	ARID3A	chr7:105172276-105172771	K562	blood:	n/a	n/a
6	ARID3A	chr7:105162675-105163137	K562	blood:	n/a	n/a
7	ARID3A	chr7:105162532-105162842	HepG2	liver:	n/a	n/a
8	ATF1	chr7:105128345-105128752	K562	blood:	n/a	n/a
9	ATF2	chr7:105171988-105172822	GM12878	blood:	n/a	n/a
10	ATF2	chr7:105162441-105162701	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:105172329-105172807	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:105172257-105172894	GM12878	blood:	n/a	n/a
13	ATF3	chr7:105172202-105172799	K562	blood:	n/a	n/a
14	ATF3	chr7:105162479-105162756	A549	lung:	n/a	chr7:105162516-105162525
15	ATF3	chr7:105162419-105162922	K562	blood:	n/a	chr7:105162516-105162525
16	BACH1	chr7:105161884-105162223	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:105172426-105172817	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:105113662-105113870	K562	blood:	n/a	n/a
19	BACH1	chr7:105113653-105113991	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:105172328-105172846	K562	blood:	n/a	n/a
21	BACH1	chr7:105162629-105162935	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr7:105172440-105172791	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:105172537-105172868	GM12878	blood:	n/a	n/a
24	BCL3	chr7:105162453-105163079	A549	lung:	n/a	chr7:105162468-105162481 chr7:105162470-105162483
25	BCL3	chr7:105172316-105172982	A549	lung:	n/a	n/a
26	BCL3	chr7:105172270-105172911	A549	lung:	n/a	n/a
27	BCLAF1	chr7:105162157-105163019	K562	blood:	n/a	chr7:105162468-105162481 chr7:105162470-105162483
28	BCLAF1	chr7:105172218-105172996	K562	blood:	n/a	n/a
29	BCLAF1	chr7:105172328-105172981	K562	blood:	n/a	n/a
30	BCLAF1	chr7:105172265-105172905	GM12878	blood:	n/a	n/a
31	BCLAF1	chr7:105172346-105172920	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:105161582-105163259	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:105172018-105173029	K562	blood:	n/a	n/a
34	BHLHE40	chr7:105162519-105162872	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:105162517-105162823	A549	lung:	n/a	n/a
36	BHLHE40	chr7:105171963-105172867	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:105161610-105163105	K562	blood:	n/a	n/a
38	BHLHE40	chr7:105128299-105128701	K562	blood:	n/a	n/a
39	BHLHE40	chr7:105174117-105174180	K562	blood:	n/a	n/a
40	BHLHE40	chr7:105172056-105172791	HepG2	liver:	n/a	n/a
41	BHLHE40	chr7:105161948-105162953	HepG2	liver:	n/a	n/a
42	BRCA1	chr7:105161980-105162068	HepG2	liver:	n/a	n/a
43	BRCA1	chr7:105172446-105172663	GM12878	blood:	n/a	n/a
44	BRCA1	chr7:105162680-105163061	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr7:105172361-105172945	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr7:105171840-105173469	K562	blood:	n/a	n/a
47	CBX3	chr7:105172354-105173016	K562	blood:	n/a	n/a
48	CBX3	chr7:105161068-105162276	K562	blood:	n/a	n/a
49	CBX3	chr7:105162379-105163324	K562	blood:	n/a	n/a
50	CBX3	chr7:105161716-105162247	K562	blood:	n/a	n/a

(count:1956 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105162855-105162905	GM12891	blood:	n/a
2	chr7:105176805-105176855	GM12878	blood:	n/a
3	chr7:105160482-105160532	AG04450	lung:	fetal
4	chr7:105158109-105158159	SK-N-SH_RA	brain:	n/a
5	chr7:105162855-105162905	GM12891	blood:	n/a
6	chr7:105176805-105176855	GM12878	blood:	n/a
7	chr7:105160482-105160532	AG04450	lung:	fetal
8	chr7:105158109-105158159	SK-N-SH_RA	brain:	n/a
9	chr7:105172664-105172714	BE2_C	brain:	n/a
10	chr7:105112740-105112790	U87	brain:	n/a
11	chr7:105162600-105162650	HMEC	breast:	n/a
12	chr7:105162859-105162909	HAEpiC	amniotic membrane:	n/a
13	chr7:105162735-105162785	HCF	heart:	n/a
14	chr7:105162577-105162627	Caco-2	colon:	n/a
15	chr7:105165592-105165642	BJ	skin:	n/a
16	chr7:105162735-105162785	HEK293	kidney:	embryo
17	chr7:105172664-105172714	ECC-1	luminal epithelium:	n/a
18	chr7:105172168-105172218	BJ	skin:	n/a
19	chr7:105134734-105134784	HIPEpiC	eye:	n/a
20	chr7:105110948-105110998	GM19239	blood:	n/a
21	chr7:105162888-105162938	NH-A	brain:	n/a
22	chr7:105176805-105176855	U87	brain:	n/a
23	chr7:105171843-105171893	H1-hESC	embryonic stem cell:	embryo
24	chr7:105172664-105172714	H1-hESC	embryonic stem cell:	embryo
25	chr7:105161983-105162033	GM06990	blood:	n/a
26	chr7:105110948-105110998	NH-A	brain:	n/a
27	chr7:105172168-105172218	AG09319	gingival:	n/a
28	chr7:105162855-105162905	MCF10A-Er-Src	breast:	n/a
29	chr7:105172403-105172453	GM12891	blood:	n/a
30	chr7:105162470-105162520	HMEC	breast:	n/a
31	chr7:105162855-105162905	HCPEpiC	choroid plexus:	n/a
32	chr7:105171843-105171893	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:105172403-105172453	RPTEC	kidney:	n/a
34	chr7:105161983-105162033	GM19239	blood:	n/a
35	chr7:105162761-105162811	GM12878	blood:	n/a
36	chr7:105162600-105162650	GM12891	blood:	n/a
37	chr7:105110948-105110998	AG10803	skin:	n/a
38	chr7:105171843-105171893	GM12891	blood:	n/a
39	chr7:105172664-105172714	CMK	blood:	n/a
40	chr7:105162470-105162520	GM12891	blood:	n/a
41	chr7:105162855-105162905	GM06990	blood:	n/a
42	chr7:105161983-105162033	NT2-D1	testis:	n/a
43	chr7:105110948-105110998	HEK293	kidney:	embryo
44	chr7:105172168-105172218	AoSMC	blood vessel:	n/a
45	chr7:105162814-105162864	Hepatocyte	liver:	n/a
46	chr7:105172168-105172218	GM12892	blood:	n/a
47	chr7:105137683-105137733	AG04449	skin:	fetal
48	chr7:105172403-105172453	H1-hESC	embryonic stem cell:	embryo
49	chr7:105173132-105173182	HUVEC	blood vessel:	n/a
50	chr7:105160482-105160532	HUVEC	blood vessel:	n/a

(count:139 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:104652163..104655972-chr7:105160292..105163807,4	MCF-7	breast:
2	chr7:105171895..105174076-chr7:105174094..105176454,2	MCF-7	breast:
3	chr7:105126748..105128626-chr7:105155718..105158086,2	K562	blood:
4	chr7:105139837..105141467-chr7:105172365..105173927,2	K562	blood:
5	chr7:105178950..105184769-chr7:105189536..105192769,5	K562	blood:
6	chr7:105108727..105111208-chr7:105115281..105117815,3	K562	blood:
7	chr11:66056148..66056859-chr7:105172413..105173177,2	Hela-S3	cervix:
8	chr1:156698268..156698938-chr7:105162358..105162859,2	Hela-S3	cervix:
9	chr7:105161102..105162655-chr7:105181498..105183213,2	K562	blood:
10	chr7:105160687..105164718-chr7:105170642..105174239,14	MCF-7	breast:
11	chr7:105139514..105141337-chr7:105172365..105174838,2	K562	blood:
12	chr7:105140985..105143756-chr7:105161298..105163196,2	K562	blood:
13	chr7:105116272..105117859-chr7:105118414..105120932,2	K562	blood:
14	chr7:105141175..105142796-chr7:105145360..105147513,2	MCF-7	breast:
15	chr7:105158727..105165017-chr7:105166972..105176993,56	K562	blood:
16	chr19:55628556..55629065-chr7:105162615..105163265,2	Hela-S3	cervix:
17	chr7:105172591..105175323-chr7:105192776..105195472,2	MCF-7	breast:
18	chr7:105171919..105174630-chr7:105210042..105212382,2	K562	blood:
19	chr7:105110346..105111937-chr7:105127717..105129867,2	K562	blood:
20	chr7:105171433..105173431-chr7:105176535..105180358,4	MCF-7	breast:
21	chr7:105160261..105165362-chr7:105168599..105174293,22	MCF-7	breast:
22	chr17:56708735..56709467-chr7:105162240..105162879,2	MCF-7	breast:
23	chr7:105162231..105163027-chr7:105172004..105172750,2	K562	blood:
24	chr7:105192153..105195079-chr7:105203440..105205877,2	K562	blood:
25	chr7:105164878..105167399-chrX:150160313..150162804,2	MCF-7	breast:
26	chr7:105165151..105169952-chr7:105171142..105174252,8	MCF-7	breast:
27	chr7:105158727..105165017-chr7:105166972..105176993,56	K562	blood:
28	chr7:105129766..105132024-chr7:105147808..105150041,2	MCF-7	breast:
29	chr7:105069185..105071026-chr7:105110310..105112272,2	MCF-7	breast:
30	chr7:104653151..104655503-chr7:105160083..105164345,7	K562	blood:
31	chr7:105128652..105130431-chr7:105155897..105157484,2	MCF-7	breast:
32	chr7:105162459..105163197-chr7:105172183..105173025,3	MCF-7	breast:
33	chr19:1261170..1262083-chr7:105162048..105162685,2	Hela-S3	cervix:
34	chr7:105171303..105174411-chr7:105176077..105181251,7	MCF-7	breast:
35	chr7:105103366..105105752-chr7:105109309..105111791,2	K562	blood:
36	chr7:104652625..104654760-chr7:105154090..105155879,2	K562	blood:
37	chr7:105121563..105123153-chr7:105161155..105163117,2	MCF-7	breast:
38	chr7:105143860..105147794-chr7:105158802..105162576,5	K562	blood:
39	chr7:104653054..104655993-chr7:105161169..105164095,3	MCF-7	breast:
40	chr1:209957159..209957989-chr7:105162027..105162579,2	Hela-S3	cervix:
41	chr7:105171071..105173381-chr7:105188092..105190983,2	MCF-7	breast:
42	chr7:105162283..105162894-chr7:105172462..105173034,2	NB4	blood:
43	chr7:105178950..105184769-chr7:105189536..105192769,5	K562	blood:
44	chr7:105161098..105164204-chr7:105164483..105168107,5	MCF-7	breast:
45	chr7:105143576..105146396-chr7:105147042..105149947,3	K562	blood:
46	chr7:105171231..105172860-chr7:105185302..105187081,2	MCF-7	breast:
47	chr7:104651944..104654760-chr7:105154090..105156667,3	K562	blood:
48	chr7:105174875..105178422-chr7:105279003..105282206,4	MCF-7	breast:
49	chr7:104652025..104655481-chr7:105171171..105174883,4	K562	blood:
50	chr7:104793384..104794011-chr7:105128109..105129098,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PUS7-1	chr7:105170677-105170904	NONHSAT122623
2	lnc-CDHR3-5	chr7:105182048-105182302	NONHSAT122624
3	lnc-RINT1-2	chr7:105170656-105171118	NONHSAT122622
4	lnc-CDHR3-5	chr7:105182855-105183003	NONHSAT122624
5	lnc-PUS7-1	chr7:105171944-105171973	NONHSAT122623

No data

Variant related genes	Relation type
RINT1	TF binding region
ENSG00000223886	TF binding region
PUS7	TF binding region
RINT1	CpG island
ENSG00000223886	CpG island
PUS7	CpG island
ENSG00000150753	chromatin interactions
ENSG00000072210	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000223886	chromatin interactions
ENSG00000230508	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000233797	chromatin interactions
ENSG00000185055	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000014123	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000162757	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000231167	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000272604	chromatin interactions

Extended variants
information (count: 3386 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3386 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2258851	chr7:105110990-105110991	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112691205	chr7:105111026-105111027	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541497843	chr7:105111041-105111042	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537565458	chr7:105111070-105111071	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201960700	chr7:105111114-105111115	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368930685	chr7:105111120-105111121	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113639774	chr7:105111144-105111145	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369396600	chr7:105111147-105111148	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550476795	chr7:105111153-105111154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200932805	chr7:105111184-105111185	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112413140	chr7:105111219-105111220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573197277	chr7:105111234-105111235	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377333257	chr7:105111300-105111301	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370352321	chr7:105111301-105111302	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374366171	chr7:105111302-105111303	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150896829	chr7:105111309-105111310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35488957	chr7:105111312-105111313	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377544089	chr7:105111324-105111325	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370756343	chr7:105111335-105111336	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570861329	chr7:105111442-105111443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75312721	chr7:105111460-105111461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368978758	chr7:105111477-105111478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574517997	chr7:105111618-105111619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188961448	chr7:105111631-105111632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567474451	chr7:105111640-105111641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191796368	chr7:105111641-105111642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs818478	chr7:105111661-105111662	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576256806	chr7:105111696-105111697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554154295	chr7:105111703-105111704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367984348	chr7:105111709-105111710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562660276	chr7:105111832-105111833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545279863	chr7:105111850-105111851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34304484	chr7:105111873-105111874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183253782	chr7:105111974-105111975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2030775	chr7:105111985-105111986	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs370662276	chr7:105111986-105111987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541561520	chr7:105111996-105111997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115286216	chr7:105112001-105112002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114331895	chr7:105112080-105112081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114782945	chr7:105112085-105112086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368525935	chr7:105112157-105112158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564054832	chr7:105112158-105112159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532666561	chr7:105112166-105112167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552412876	chr7:105112177-105112178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113340544	chr7:105112223-105112224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372213559	chr7:105112244-105112245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527264935	chr7:105112267-105112268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547505780	chr7:105112273-105112274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537582167	chr7:105112310-105112311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs397942320	chr7:105112375-105112376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:2787 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105080000-105161200	Weak transcription	Pancreas	Pancrea
2	chr7:105080200-105126800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr7:105088200-105142600	Weak transcription	Esophagus	oesophagus
4	chr7:105088200-105152800	Weak transcription	Gastric	stomach
5	chr7:105088400-105140400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr7:105089200-105127000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr7:105089200-105142600	Weak transcription	Fetal Thymus	thymus
8	chr7:105089600-105145200	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr7:105089600-105145800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:105090000-105126800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr7:105090000-105128200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr7:105090800-105120200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr7:105093400-105112600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:105093600-105153000	Weak transcription	Small Intestine	intestine
15	chr7:105094400-105113400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr7:105094400-105120200	Weak transcription	Lung	lung
17	chr7:105094800-105137200	Weak transcription	Fetal Kidney	kidney
18	chr7:105095000-105128200	Weak transcription	Primary B cells from cord blood	blood
19	chr7:105095200-105113000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr7:105095200-105140600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr7:105095200-105142600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:105095600-105128400	Weak transcription	Brain Angular Gyrus	brain
23	chr7:105095600-105128400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:105096000-105113000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:105096000-105119200	Weak transcription	Brain Anterior Caudate	brain
26	chr7:105096000-105126400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:105096000-105127600	Weak transcription	NHLF	lung
28	chr7:105096000-105141000	Weak transcription	Colonic Mucosa	Colon
29	chr7:105096200-105128200	Weak transcription	Brain Hippocampus Middle	brain
30	chr7:105096400-105128000	Weak transcription	Brain Substantia Nigra	brain
31	chr7:105096400-105145600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr7:105096600-105112600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr7:105096600-105113200	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr7:105096600-105113400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr7:105098200-105151200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr7:105098600-105111200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr7:105098600-105121000	Weak transcription	Brain Germinal Matrix	brain
38	chr7:105098600-105128400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr7:105098800-105119200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr7:105099400-105130800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr7:105099800-105127600	Weak transcription	NHDF-Ad	bronchial
42	chr7:105099800-105153000	Weak transcription	Psoas Muscle	Psoas
43	chr7:105100000-105141800	Weak transcription	Placenta	Placenta
44	chr7:105102000-105121000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr7:105102400-105113800	Weak transcription	Adipose Nuclei	Adipose
46	chr7:105102400-105118800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:105102400-105119600	Weak transcription	Duodenum Mucosa	Duodenum
48	chr7:105102400-105120600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr7:105102400-105128000	Weak transcription	Fetal Lung	lung
50	chr7:105102400-105134000	Weak transcription	Aorta	Aorta

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