Variant report

Variant	esv1795451
Chromosome Location	chr7:140155800-140163131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:61)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:61 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:140155335-140155960	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:140155563-140155898	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr7:140156571-140156867	HepG2	liver:	n/a	n/a
4	CHD2	chr7:140155503-140155895	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr7:140156671-140156740	GM13976	blood:	n/a	n/a
6	E2F6	chr7:140155654-140156016	H1-hESC	embryonic stem cell:	n/a	n/a
7	FOS	chr7:140156687-140156813	MCF10A-Er-Src	breast:	n/a	n/a
8	FOXA1	chr7:140156632-140157029	HepG2	liver:	n/a	chr7:140156979-140156991 chr7:140156840-140156852 chr7:140156844-140156856
9	FOXA1	chr7:140156606-140157039	HepG2	liver:	n/a	chr7:140156979-140156991 chr7:140156840-140156852 chr7:140156844-140156856
10	FOXA1	chr7:140156662-140156974	HepG2	liver:	n/a	chr7:140156840-140156852 chr7:140156844-140156856
11	FOXA2	chr7:140156639-140156953	HepG2	liver:	n/a	chr7:140156840-140156852 chr7:140156844-140156856
12	GATA3	chr7:140157740-140158008	SH-SY5Y	brain:	n/a	n/a
13	HDAC2	chr7:140155520-140155911	H1-hESC	embryonic stem cell:	n/a	n/a
14	JUND	chr7:140155322-140155965	H1-hESC	embryonic stem cell:	n/a	n/a
15	MAX	chr7:140155534-140155992	H1-hESC	embryonic stem cell:	n/a	chr7:140155807-140155814 chr7:140155806-140155816 chr7:140155806-140155815 chr7:140155805-140155816
16	MAX	chr7:140155513-140156021	H1-hESC	embryonic stem cell:	n/a	chr7:140155807-140155814 chr7:140155806-140155816 chr7:140155806-140155815 chr7:140155805-140155816
17	MAX	chr7:140155490-140156065	H1-hESC	embryonic stem cell:	n/a	chr7:140155807-140155814 chr7:140155806-140155816 chr7:140155806-140155815 chr7:140155805-140155816
18	MXI1	chr7:140155593-140156014	H1-hESC	embryonic stem cell:	n/a	n/a
19	MYC	chr7:140155669-140156037	H1-hESC	embryonic stem cell:	n/a	chr7:140155807-140155814 chr7:140155806-140155816 chr7:140155806-140155815 chr7:140155805-140155816
20	MYC	chr7:140156877-140156903	H1-hESC	embryonic stem cell:	n/a	n/a
21	NANOG	chr7:140155587-140155845	H1-hESC	embryonic stem cell:	n/a	n/a
22	PAX5	chr7:140161828-140161998	GM12878	blood:	n/a	n/a
23	POLR2A	chr7:140155678-140155915	K562	blood:	n/a	n/a
24	POLR2A	chr7:140157029-140157670	K562	blood:	n/a	n/a
25	POLR2A	chr7:140162899-140163354	K562	blood:	n/a	n/a
26	POLR2A	chr7:140156761-140157236	K562	blood:	n/a	n/a
27	POLR2A	chr7:140162731-140162916	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr7:140155634-140155804	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr7:140160532-140161348	K562	blood:	n/a	n/a
30	POLR2A	chr7:140162980-140163347	GM12878	blood:	n/a	n/a
31	POLR2A	chr7:140162962-140163143	HepG2	liver:	n/a	n/a
32	POLR2A	chr7:140155398-140155847	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr7:140155222-140155909	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr7:140155074-140156134	HepG2	liver:	n/a	n/a
35	POLR2A	chr7:140157557-140159917	K562	blood:	n/a	n/a
36	POLR2A	chr7:140157855-140158227	HepG2	liver:	n/a	n/a
37	POLR2A	chr7:140156517-140156612	Gliobla	brain:	n/a	n/a
38	POLR2A	chr7:140156064-140156170	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr7:140161675-140161721	ProgFib	skin:	n/a	n/a
40	POLR2A	chr7:140163032-140163248	HepG2	liver:	n/a	n/a
41	POLR2A	chr7:140154871-140156100	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr7:140161953-140162005	K562	blood:	n/a	n/a
43	POLR2A	chr7:140150817-140156302	K562	blood:	n/a	n/a
44	POLR2A	chr7:140156481-140156513	Gliobla	brain:	n/a	n/a
45	RAD21	chr7:140155512-140155927	H1-hESC	embryonic stem cell:	n/a	n/a
46	SIN3A	chr7:140155556-140155995	H1-hESC	embryonic stem cell:	n/a	n/a
47	SIN3AK20	chr7:140155643-140155852	H1-hESC	embryonic stem cell:	n/a	n/a
48	SP1	chr7:140155365-140155913	H1-hESC	embryonic stem cell:	n/a	n/a
49	STAT3	chr7:140160645-140160765	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr7:140156586-140156832	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140156225-140156275	Jurkat	blood:	n/a
2	chr7:140156225-140156275	HCT-116	colon:	n/a
3	chr7:140156225-140156275	PrEC	prostate:	n/a
4	chr7:140156225-140156275	IMR90	lung:	fetal
5	chr7:140156225-140156275	LNCaP	prostate:	n/a
6	chr7:140156225-140156275	AoSMC	blood vessel:	n/a
7	chr7:140156225-140156275	HUVEC	blood vessel:	n/a
8	chr7:140156225-140156275	AG09309	skin:	n/a
9	chr7:140156225-140156275	PANC-1	pancreas:	n/a
10	chr7:140156225-140156275	HCM	heart:	n/a
11	chr7:140156225-140156275	HRCEpiC	kidney:	n/a
12	chr7:140156225-140156275	AG04450	lung:	fetal
13	chr7:140156225-140156275	NB4	blood:	n/a
14	chr7:140156225-140156275	HAEpiC	amniotic membrane:	n/a
15	chr7:140156225-140156275	HRPEpiC	eye:	n/a
16	chr7:140156225-140156275	HRE	kidney:	n/a
17	chr7:140156225-140156275	AG04449	skin:	fetal
18	chr7:140156225-140156275	HepG2	liver:	n/a
19	chr7:140156225-140156275	K562	blood:	n/a
20	chr7:140156225-140156275	U87	brain:	n/a
21	chr7:140156225-140156275	GM12891	blood:	n/a
22	chr7:140156225-140156275	ovcar-3	ovarian:	n/a
23	chr7:140156225-140156275	MCF-7	breast:	n/a
24	chr7:140156225-140156275	HMEC	breast:	n/a
25	chr7:140156225-140156275	HCPEpiC	choroid plexus:	n/a
26	chr7:140156225-140156275	GM12878	blood:	n/a
27	chr7:140156225-140156275	BE2_C	brain:	n/a
28	chr7:140156225-140156275	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:140156225-140156275	SK-N-SH	brain:	n/a
30	chr7:140156225-140156275	RPTEC	kidney:	n/a
31	chr7:140156225-140156275	GM12892	blood:	n/a
32	chr7:140156225-140156275	GM19239	blood:	n/a
33	chr7:140156225-140156275	BJ	skin:	n/a
34	chr7:140156225-140156275	T-47D	breast:	n/a
35	chr7:140156225-140156275	Hepatocyte	liver:	n/a
36	chr7:140156225-140156275	AG09319	gingival:	n/a
37	chr7:140156225-140156275	H1-hESC	embryonic stem cell:	embryo
38	chr7:140156225-140156275	MCF10A-Er-Src	breast:	n/a
39	chr7:140156225-140156275	SK-N-MC	brain:	n/a
40	chr7:140156225-140156275	NHDF-neo	bronchial:	n/a
41	chr7:140156225-140156275	NT2-D1	testis:	n/a
42	chr7:140156225-140156275	SKMC	muscle:	n/a
43	chr7:140156225-140156275	A549	lung:	n/a
44	chr7:140156225-140156275	ECC-1	luminal epithelium:	n/a
45	chr7:140156225-140156275	HL-60	blood:	n/a
46	chr7:140156225-140156275	AG10803	skin:	n/a
47	chr7:140156225-140156275	HEEpiC	esophagus:	n/a
48	chr7:140156225-140156275	NHBE	bronchial:	n/a
49	chr7:140156225-140156275	PFSK-1	brain:	n/a
50	chr7:140156225-140156275	HCF	heart:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:140159764..140161788-chr7:140164687..140167007,2	K562	blood:
2	chr7:140161284..140163176-chr7:140165152..140167509,2	K562	blood:
3	chr7:140157011..140159254-chr7:140159407..140161490,2	K562	blood:
4	chr7:140147282..140150132-chr7:140156885..140159416,3	K562	blood:
5	chr7:140157011..140159254-chr7:140159407..140161490,2	K562	blood:
6	chr7:140155139..140157555-chr7:140177850..140179410,2	K562	blood:
7	chr7:140154066..140157703-chr7:140158692..140161439,4	K562	blood:
8	chr7:140158988..140161264-chr7:140165507..140167468,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MKRN1	hsa-miR-375	chr7:140156047-140156068

Variant related genes	Relation type
MKRN1	TF binding region
MKRN1	CpG island
ENSG00000133606	chromatin interactions

Extended variants
information (count: 319 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17621014	chr7:140155800-140155801	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs564429344	chr7:140155811-140155812	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs139345958	chr7:140155824-140155825	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573238460	chr7:140155837-140155838	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs150044172	chr7:140155874-140155875	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs80120731	chr7:140155915-140155916	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs75813913	chr7:140155926-140155927	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs57991505	chr7:140155928-140155929	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs556675115	chr7:140155946-140155947	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534204731	chr7:140155969-140155970	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs552570079	chr7:140155995-140155996	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571154767	chr7:140155996-140155997	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540488364	chr7:140156146-140156147	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs569542124	chr7:140156155-140156156	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs538030424	chr7:140156274-140156275	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs185986740	chr7:140156278-140156279	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144344762	chr7:140156340-140156341	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs535901709	chr7:140156343-140156344	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs1062771	chr7:140156454-140156455	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs1139716	chr7:140156456-140156457	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs1062770	chr7:140156474-140156475	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs562305064	chr7:140156475-140156476	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs1062769	chr7:140156512-140156513	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554245561	chr7:140156523-140156524	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1062768	chr7:140156548-140156549	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs1062767	chr7:140156553-140156554	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs1062766	chr7:140156554-140156555	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs368646881	chr7:140156580-140156581	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs372241410	chr7:140156598-140156599	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs1062765	chr7:140156602-140156603	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376798349	chr7:140156614-140156615	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs1062764	chr7:140156622-140156623	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577097233	chr7:140156675-140156676	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs78256678	chr7:140156723-140156724	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs576745848	chr7:140156758-140156759	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs77526235	chr7:140156789-140156790	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs572306848	chr7:140156794-140156795	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs551344907	chr7:140156811-140156812	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs61226924	chr7:140156834-140156835	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs563167032	chr7:140156840-140156841	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146223954	chr7:140156841-140156842	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201881699	chr7:140156843-140156844	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373579178	chr7:140156852-140156853	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560659561	chr7:140156859-140156860	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs527655336	chr7:140156860-140156861	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs530434859	chr7:140156867-140156868	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs140991189	chr7:140156908-140156909	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs190659838	chr7:140156970-140156971	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs375369335	chr7:140157017-140157018	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs552104862	chr7:140157034-140157035	Genic enhancers Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19826477	CNVD
Melanoma	19509136	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140126400-140176600	Weak transcription	Right Atrium	heart
2	chr7:140135800-140156000	Weak transcription	NHEK	skin
3	chr7:140150800-140171800	Strong transcription	Fetal Thymus	thymus
4	chr7:140151000-140156200	Strong transcription	Fetal Brain Female	brain
5	chr7:140151000-140171600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:140151000-140171600	Strong transcription	Duodenum Smooth Muscle	Duodenum
7	chr7:140151000-140173400	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr7:140151200-140160600	Weak transcription	Stomach Mucosa	stomach
9	chr7:140151200-140161800	Strong transcription	Placenta	Placenta
10	chr7:140151200-140171600	Strong transcription	Adipose Nuclei	Adipose
11	chr7:140151200-140172200	Strong transcription	Fetal Stomach	stomach
12	chr7:140151400-140156200	Strong transcription	Fetal Intestine Large	intestine
13	chr7:140151400-140156800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:140151400-140157200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:140151400-140161000	Strong transcription	Primary B cells from cord blood	blood
16	chr7:140151400-140162400	Strong transcription	Thymus	Thymus
17	chr7:140151400-140163600	Strong transcription	Primary T cells from cord blood	blood
18	chr7:140151400-140171800	Strong transcription	Primary B cells from peripheral blood	blood
19	chr7:140151400-140172200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr7:140151600-140156000	Strong transcription	Brain Cingulate Gyrus	brain
21	chr7:140151600-140157800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:140151600-140172200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr7:140151800-140155800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:140151800-140172200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr7:140151800-140176600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:140152200-140156400	Strong transcription	Liver	Liver
27	chr7:140152200-140157600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:140152200-140159000	Strong transcription	Left Ventricle	heart
29	chr7:140152200-140163000	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr7:140152200-140163000	Strong transcription	Fetal Muscle Leg	muscle
31	chr7:140152200-140171400	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr7:140152200-140172000	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr7:140152200-140172000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr7:140152200-140172000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:140152200-140172200	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr7:140152400-140163400	Strong transcription	Dnd41	blood
37	chr7:140152400-140166400	Strong transcription	Duodenum Mucosa	Duodenum
38	chr7:140152400-140171600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:140152400-140171600	Strong transcription	Stomach Smooth Muscle	stomach
40	chr7:140152400-140171800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:140152400-140172200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:140152600-140155800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr7:140152600-140155800	Strong transcription	Colon Smooth Muscle	Colon
44	chr7:140152600-140159000	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr7:140152600-140159200	Strong transcription	NHDF-Ad	bronchial
46	chr7:140152600-140159800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr7:140152600-140161400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:140152600-140165800	Strong transcription	Spleen	Spleen
49	chr7:140152600-140167400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:140152600-140171800	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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