Variant report

Variant	esv2761087
Chromosome Location	chr7:124823624-125429662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1942)
CpG islands
(count:122)
Chromatin interactive
region (count:113)
LncRNA
region (count:57)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1942 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:125235405-125235419	K562	blood:	n/a	n/a
2	ARID3A	chr7:125238528-125238531	K562	blood:	n/a	n/a
3	ARID3A	chr7:125245371-125245822	K562	blood:	n/a	n/a
4	ARID3A	chr7:125207883-125208163	K562	blood:	n/a	n/a
5	ARID3A	chr7:125036847-125037232	K562	blood:	n/a	n/a
6	ARID3A	chr7:125145112-125145113	K562	blood:	n/a	n/a
7	ARID3A	chr7:124896704-124896904	K562	blood:	n/a	n/a
8	ARID3A	chr7:125112702-125112705	K562	blood:	n/a	n/a
9	ATF1	chr7:125036628-125037136	K562	blood:	n/a	n/a
10	ATF1	chr7:125155568-125155672	K562	blood:	n/a	n/a
11	ATF1	chr7:125099017-125099154	K562	blood:	n/a	n/a
12	ATF1	chr7:125102482-125102530	K562	blood:	n/a	n/a
13	ATF1	chr7:125304902-125304935	K562	blood:	n/a	n/a
14	ATF2	chr7:125208736-125209317	GM12878	blood:	n/a	n/a
15	ATF2	chr7:125292085-125292579	GM12878	blood:	n/a	n/a
16	ATF2	chr7:124995927-124996331	GM12878	blood:	n/a	n/a
17	ATF2	chr7:125208800-125209277	GM12878	blood:	n/a	n/a
18	ATF2	chr7:124995766-124996416	GM12878	blood:	n/a	n/a
19	ATF3	chr7:125036857-125037111	K562	blood:	n/a	n/a
20	ATF3	chr7:124956558-124956827	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr7:125245272-125245589	K562	blood:	n/a	n/a
22	ATF3	chr7:124956563-124956950	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:125250853-125250856	K562	blood:	n/a	n/a
24	BACH1	chr7:125144988-125145184	K562	blood:	n/a	n/a
25	BACH1	chr7:124927356-124927377	K562	blood:	n/a	n/a
26	BACH1	chr7:125144864-125145256	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:124912339-124912344	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:125245462-125245548	H1-hESC	embryonic stem cell:	n/a	chr7:125245471-125245485
29	BATF	chr7:125144978-125145174	GM12878	blood:	n/a	chr7:125145074-125145085
30	BATF	chr7:124996043-124996381	GM12878	blood:	n/a	n/a
31	BATF	chr7:125400561-125400782	GM12878	blood:	n/a	n/a
32	BATF	chr7:125208879-125209269	GM12878	blood:	n/a	n/a
33	BATF	chr7:125131056-125131238	GM12878	blood:	n/a	n/a
34	BATF	chr7:125208852-125209217	GM12878	blood:	n/a	n/a
35	BATF	chr7:124996009-124996436	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:125208879-125209307	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:124995894-124996370	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:125208927-125209202	GM12878	blood:	n/a	n/a
39	BCL3	chr7:125292138-125292574	GM12878	blood:	n/a	n/a
40	BCL3	chr7:124995875-124996328	GM12878	blood:	n/a	n/a
41	BCL3	chr7:125208897-125209206	GM12878	blood:	n/a	n/a
42	BCLAF1	chr7:125208875-125209224	GM12878	blood:	n/a	n/a
43	BCLAF1	chr7:125208811-125209257	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:125052988-125053632	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:125375284-125375348	K562	blood:	n/a	n/a
46	BHLHE40	chr7:125201165-125201410	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:125178945-125179203	K562	blood:	n/a	chr7:125179077-125179098 chr7:125179081-125179094
48	BHLHE40	chr7:125301808-125302109	K562	blood:	n/a	n/a
49	BHLHE40	chr7:125208861-125209208	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:124995944-124996351	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124898559-124898609	HEEpiC	esophagus:	n/a
2	chr7:124904981-124905031	NH-A	brain:	n/a
3	chr7:124904981-124905031	HMEC	breast:	n/a
4	chr7:124904981-124905031	SK-N-SH	brain:	n/a
5	chr7:124904981-124905031	ovcar-3	ovarian:	n/a
6	chr7:124904981-124905031	Hela-S3	cervix:	n/a
7	chr7:124898559-124898609	BE2_C	brain:	n/a
8	chr7:124898559-124898609	SK-N-SH	brain:	n/a
9	chr7:124904981-124905031	RPTEC	kidney:	n/a
10	chr7:124898559-124898609	IMR90	lung:	fetal
11	chr7:124904981-124905031	A549	lung:	n/a
12	chr7:124898559-124898609	NHDF-neo	bronchial:	n/a
13	chr7:124904981-124905031	MCF-7	breast:	n/a
14	chr7:124904981-124905031	HRE	kidney:	n/a
15	chr7:124904981-124905031	Hepatocyte	liver:	n/a
16	chr7:124898559-124898609	AG04450	lung:	fetal
17	chr7:124904981-124905031	HRPEpiC	eye:	n/a
18	chr7:124904981-124905031	IMR90	lung:	fetal
19	chr7:124898559-124898609	K562	blood:	n/a
20	chr7:124898559-124898609	LNCaP	prostate:	n/a
21	chr7:124904981-124905031	SK-N-SH_RA	brain:	n/a
22	chr7:124898559-124898609	GM12878	blood:	n/a
23	chr7:124904981-124905031	ECC-1	luminal epithelium:	n/a
24	chr7:124898559-124898609	HAEpiC	amniotic membrane:	n/a
25	chr7:124904981-124905031	HCM	heart:	n/a
26	chr7:124904981-124905031	HRCEpiC	kidney:	n/a
27	chr7:124898559-124898609	GM19239	blood:	n/a
28	chr7:124898559-124898609	Jurkat	blood:	n/a
29	chr7:124904981-124905031	Caco-2	colon:	n/a
30	chr7:124904981-124905031	AG10803	skin:	n/a
31	chr7:124904981-124905031	ProgFib	skin:	n/a
32	chr7:124904981-124905031	PrEC	prostate:	n/a
33	chr7:124898559-124898609	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:124898559-124898609	HL-60	blood:	n/a
35	chr7:124904981-124905031	GM12878	blood:	n/a
36	chr7:124904981-124905031	PANC-1	pancreas:	n/a
37	chr7:124904981-124905031	NT2-D1	testis:	n/a
38	chr7:124898559-124898609	ECC-1	luminal epithelium:	n/a
39	chr7:124898559-124898609	HNPCEpiC	eye:	n/a
40	chr7:124898559-124898609	NHBE	bronchial:	n/a
41	chr7:124904981-124905031	SAEC	small airway:	n/a
42	chr7:124898559-124898609	PANC-1	pancreas:	n/a
43	chr7:124898559-124898609	HCPEpiC	choroid plexus:	n/a
44	chr7:124904981-124905031	HepG2	liver:	n/a
45	chr7:124904981-124905031	HIPEpiC	eye:	n/a
46	chr7:124904981-124905031	AG04450	lung:	fetal
47	chr7:124898559-124898609	MCF10A-Er-Src	breast:	n/a
48	chr7:124898559-124898609	CMK	blood:	n/a
49	chr7:124898559-124898609	AG09309	skin:	n/a
50	chr7:124904981-124905031	PFSK-1	brain:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:125269070..125270794-chr7:125275616..125278202,2	K562	blood:
2	chr7:125023517..125024026-chr7:125310752..125311652,2	MCF-7	breast:
3	chr7:124846681..124848535-chr7:125206338..125208006,2	K562	blood:
4	chr7:125243932..125247685-chr7:125249366..125252787,4	K562	blood:
5	chr7:124699671..124700472-chr7:125310284..125311293,4	MCF-7	breast:
6	chr7:124656588..124658906-chr7:124962987..124965229,2	K562	blood:
7	chr7:125126724..125128959-chr7:125132341..125134111,2	K562	blood:
8	chr7:125385605..125387936-chr7:125388625..125390972,2	K562	blood:
9	chr7:125384743..125387377-chr7:125395816..125398229,2	K562	blood:
10	chr7:125385463..125387105-chr7:125388625..125390168,2	K562	blood:
11	chr7:125392984..125395323-chr7:125485232..125486912,2	K562	blood:
12	chr7:124980320..124982022-chr7:124985560..124987145,2	K562	blood:
13	chr7:124701709..124702473-chr7:124956278..124956931,2	MCF-7	breast:
14	chr7:124914060..124916364-chr7:124917880..124920305,2	K562	blood:
15	chr7:125338629..125340672-chr7:125343129..125344648,2	K562	blood:
16	chr7:125203772..125205320-chr7:125225530..125228131,2	K562	blood:
17	chr7:125241383..125243591-chr7:125245619..125247438,2	K562	blood:
18	chr7:124965414..124966985-chr7:125006930..125009873,2	K562	blood:
19	chr7:125044926..125048888-chr7:125049294..125054485,5	K562	blood:
20	chr7:124904732..124906870-chr7:124909560..124912125,2	K562	blood:
21	chr7:125243932..125247685-chr7:125249366..125252787,4	K562	blood:
22	chr7:125125355..125128224-chr7:125131443..125135163,4	K562	blood:
23	chr7:124699717..124700520-chr7:124956250..124957181,4	MCF-7	breast:
24	chr7:125226088..125228401-chr7:125230345..125233728,3	K562	blood:
25	chr7:125203772..125205320-chr7:125225530..125228131,2	K562	blood:
26	chr7:125118097..125121016-chr7:125124179..125126346,2	K562	blood:
27	chr7:125172761..125175135-chr7:125186431..125188601,2	K562	blood:
28	chr7:125369632..125371193-chr7:125372789..125375510,2	K562	blood:
29	chr7:125384743..125387377-chr7:125395816..125398229,2	K562	blood:
30	chr7:125310080..125313010-chr7:125315945..125318441,2	K562	blood:
31	chr7:125269070..125270794-chr7:125275616..125278202,2	K562	blood:
32	chr7:125190321..125191930-chr7:125194449..125196273,2	K562	blood:
33	chr7:124878093..124880264-chr7:124889805..124892447,2	MCF-7	breast:
34	chr7:125089598..125092751-chr7:125096828..125101024,3	K562	blood:
35	chr7:124885290..124887904-chr7:124890626..124892616,2	MCF-7	breast:
36	chr7:124699605..124700536-chr7:124955869..124957164,4	MCF-7	breast:
37	chr7:125014089..125016137-chr7:125017840..125020682,3	K562	blood:
38	chr7:125391124..125394118-chr7:125397604..125400061,2	K562	blood:
39	chr7:125070959..125073239-chr7:125075739..125078658,3	K562	blood:
40	chr7:124699558..124701618-chr7:125055753..125057701,2	K562	blood:
41	chr7:125204110..125205826-chr7:125284105..125286281,2	K562	blood:
42	chr7:125385463..125387105-chr7:125388625..125390168,2	K562	blood:
43	chr6:38756306..38758851-chr7:124960777..124963063,2	MCF-7	breast:
44	chr7:125218658..125220340-chr7:125222287..125223970,2	K562	blood:
45	chr7:125108997..125111782-chr7:125114989..125116888,2	K562	blood:
46	chr7:124914060..124916364-chr7:124917880..124920305,2	K562	blood:
47	chr7:125251686..125253446-chr7:125261235..125263882,2	K562	blood:
48	chr7:125234853..125237677-chr7:125237685..125240938,4	K562	blood:
49	chr7:125280203..125282931-chr7:125290069..125292178,2	K562	blood:
50	chr7:125234594..125236456-chr7:125238613..125240921,2	K562	blood:

(count:57 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-6	chr7:125071401-125071647	NONHSAT123109
2	lnc-SPAM1-5	chr7:124970311-124970457	NR_110188
3	lnc-SPAM1-5	chr7:124969736-124969801	ENSG00000237764.2
4	lnc-SPAM1-5	chr7:124835002-124835138	ENSG00000237764.2
5	lnc-SPAM1-5	chr7:125019112-125019375	NONHSAT123102
6	lnc-SPAM1-8	chr7:124985023-124985431	NONHSAT123106
7	lnc-POT1-2	chr7:124888355-124888495	NR_110183
8	lnc-POT1-2	chr7:124899849-124900056	NONHSAT123104
9	lnc-SPAM1-5	chr7:124824623-124824667	NR_110188
10	lnc-SPAM1-6	chr7:125101535-125101923	NONHSAT123109
11	lnc-SPAM1-5	chr7:124969736-124969801	NONHSAT123102
12	lnc-SPAM1-5	chr7:124987179-124987261	ENSG00000237764.2
13	lnc-SPAM1-5	chr7:125003489-125003570	ENSG00000237764.2
14	lnc-SPAM1-5	chr7:124826098-124826546	ENSG00000237764.2
15	lnc-SPAM1-6	chr7:125078199-125078351	ENSG00000227869
16	lnc-SPAM1-5	chr7:124824623-124824667	ENSG00000237764.2
17	lnc-SPAM1-5	chr7:125003489-125003570	NR_110188
18	lnc-SPAM1-5	chr7:124835002-124835138	NONHSAT123102
19	lnc-POT1-2	chr7:124904097-124904345	ENSG00000219445
20	lnc-SPAM1-6	chr7:125078276-125078351	ENSG00000227869
21	lnc-POT1-2	chr7:124890034-124890111	NR_110183
22	lnc-SPAM1-5	chr7:125019112-125019375	ENSG00000237764.2
23	lnc-SPAM1-5	chr7:124975307-124975469	NONHSAT123102
24	lnc-SPAM1-5	chr7:124970311-124970457	ENSG00000237764.2
25	lnc-SPAM1-5	chr7:124826098-124826546	NONHSAT123102
26	lnc-POT1-2	chr7:124888355-124888495	ENSG00000219445
27	lnc-SPAM1-5	chr7:124826098-124826546	NR_110188
28	lnc-SPAM1-6	chr7:125078165-125078351	ENSG00000227869
29	lnc-SPAM1-6	chr7:125106324-125106455	ENSG00000227869
30	lnc-POT1-2	chr7:124904097-124904345	NR_110183
31	lnc-POT1-2	chr7:124869633-124870895	ENSG00000219445
32	lnc-SPAM1-5	chr7:125019112-125019375	NR_110188
33	lnc-SPAM1-6	chr7:125071401-125071647	ENSG00000227869
34	lnc-SPAM1-5	chr7:124987179-124987261	NONHSAT123102
35	lnc-POT1-2	chr7:124886398-124886584	ENSG00000219445
36	lnc-SPAM1-6	chr7:125101535-125101704	ENSG00000227869
37	lnc-SPAM1-5	chr7:124975307-124975469	ENSG00000237764.2
38	lnc-SPAM1-6	chr7:125101535-125101923	ENSG00000227869
39	lnc-POT1-2	chr7:124890034-124890111	ENSG00000219445
40	lnc-POT1-2	chr7:124870622-124870895	NONHSAT123104
41	lnc-SPAM1-5	chr7:124987179-124987261	NR_110188
42	lnc-POT1-2	chr7:124870580-124870614	NONHSAT123104
43	lnc-SPAM1-5	chr7:124970311-124970457	NONHSAT123102
44	lnc-SPAM1-5	chr7:124835002-124835138	NR_110188
45	lnc-POT1-2	chr7:124888355-124888495	NONHSAT123104
46	lnc-SPAM1-5	chr7:124975307-124975469	NR_110188
47	lnc-SPAM1-5	chr7:124824624-124824667	NONHSAT123102
48	lnc-SPAM1-6	chr7:125101535-125101665	ENSG00000227869
49	lnc-POT1-2	chr7:124869633-124870895	NR_110183
50	lnc-POT1-2	chr7:124890034-124890111	NONHSAT123104

No data

Variant related genes	Relation type
ENSG00000227869	TF binding region
ENSG00000227847	TF binding region
ENSG00000234071	TF binding region
ENSG00000213291	TF binding region
ENSG00000219445	TF binding region
ENSG00000227869	CpG island
ENSG00000227847	CpG island
ENSG00000234071	CpG island
ENSG00000213291	CpG island
ENSG00000219445	CpG island
ENSG00000106302	chromatin interactions
ENSG00000227847	chromatin interactions
ENSG00000227869	chromatin interactions
SOCS6	miRNA target sites
ILF2	miRNA target sites
PHF10	miRNA target sites

Extended variants
information (count: 11892 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:11892 , 50 per page) page: 1 2 3 4 5 6 7 ... 238

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568259261	chr7:124823634-124823635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534033338	chr7:124823666-124823667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140241460	chr7:124823687-124823688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78586004	chr7:124823694-124823695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369432075	chr7:124823720-124823721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539117588	chr7:124823721-124823722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555754195	chr7:124823739-124823740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116575798	chr7:124823742-124823743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544582617	chr7:124823743-124823744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555293419	chr7:124823789-124823790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145527446	chr7:124823790-124823791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs792636	chr7:124823832-124823833	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs560648009	chr7:124823946-124823947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186059890	chr7:124823950-124823951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189950530	chr7:124824007-124824008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562872223	chr7:124824017-124824018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531777504	chr7:124824044-124824045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28402853	chr7:124824093-124824094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs568377884	chr7:124824143-124824144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs792637	chr7:124824179-124824180	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs547210246	chr7:124824193-124824194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368226221	chr7:124824224-124824225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539158590	chr7:124824311-124824312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555795246	chr7:124824319-124824320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138150777	chr7:124824345-124824346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs792638	chr7:124824349-124824350	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555053636	chr7:124824387-124824388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575105740	chr7:124824432-124824433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146630955	chr7:124824442-124824443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377432389	chr7:124824443-124824444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551626344	chr7:124824465-124824466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151276800	chr7:124824515-124824516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540902155	chr7:124824524-124824525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74622127	chr7:124824553-124824554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577466586	chr7:124824580-124824581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs180937624	chr7:124824599-124824600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199615413	chr7:124824609-124824610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565592552	chr7:124824610-124824611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201812030	chr7:124824611-124824612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs13227557	chr7:124824614-124824615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs398048083	chr7:124824618-124824619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200497727	chr7:124824619-124824620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13227560	chr7:124824623-124824624	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs563039657	chr7:124824624-124824625	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs13227561	chr7:124824625-124824626	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs13227576	chr7:124824658-124824659	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs13227581	chr7:124824669-124824670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531696030	chr7:124824679-124824680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13240221	chr7:124824684-124824685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376233621	chr7:124824701-124824702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
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
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
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20858243	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124822200-124829600	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr7:124822400-124827200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:124824800-124825400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:124825400-124832400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:124825800-124826400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:124826400-124828200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr7:124827200-124827400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
8	chr7:124828600-124828800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:124832400-124833000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:124832600-124834000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
11	chr7:124832600-124834000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:124832600-124834200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:124833000-124834600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:124833000-124836800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr7:124833200-124834000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:124833800-124834000	Enhancers	Fetal Brain Male	brain
17	chr7:124834200-124835400	Weak transcription	Fetal Brain Male	brain
18	chr7:124834600-124834800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:124834600-124834800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:124835000-124835200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr7:124835400-124835800	Enhancers	Fetal Brain Male	brain
22	chr7:124835800-124836800	Weak transcription	Fetal Brain Male	brain
23	chr7:124836600-124837000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:124836600-124838000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr7:124836600-124838400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:124837000-124837400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:124837400-124837600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:124837600-124838400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:124837600-124838400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr7:124837600-124840000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:124837800-124838000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr7:124837800-124838400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr7:124837800-124838400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:124837800-124838400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr7:124838000-124838800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr7:124838400-124839400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr7:124838400-124839400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr7:124838400-124839400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr7:124838400-124839600	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr7:124838400-124842000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr7:124838400-124842200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr7:124839400-124840000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr7:124839400-124840200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr7:124839600-124839800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr7:124839600-124839800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr7:124839600-124840000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr7:124839800-124840800	Enhancers	H1 Cell Line	embryonic stem cell
48	chr7:124840000-124840200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:124840000-124841200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr7:124840000-124841600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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