Variant report

Variant	nsv971181
Chromosome Location	chr7:99757433-99769748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:387)
CpG islands
(count:1160)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99766259-99766444	K562	blood:	n/a	chr7:99766295-99766310
2	ARID3A	chr7:99765530-99765812	K562	blood:	n/a	n/a
3	ATF1	chr7:99765519-99765767	K562	blood:	n/a	n/a
4	ATF3	chr7:99760729-99760978	K562	blood:	n/a	n/a
5	BACH1	chr7:99768819-99768999	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:99764901-99765826	K562	blood:	n/a	n/a
7	BHLHE40	chr7:99760802-99760980	K562	blood:	n/a	n/a
8	BHLHE40	chr7:99766360-99766364	K562	blood:	n/a	n/a
9	BRCA1	chr7:99766774-99767016	HepG2	liver:	n/a	n/a
10	CBX3	chr7:99765397-99765866	K562	blood:	n/a	n/a
11	CBX3	chr7:99766055-99766739	K562	blood:	n/a	n/a
12	CCNT2	chr7:99765437-99765910	K562	blood:	n/a	chr7:99765780-99765789
13	CCNT2	chr7:99766179-99766343	K562	blood:	n/a	n/a
14	CCNT2	chr7:99764900-99765160	K562	blood:	n/a	n/a
15	CEBPB	chr7:99761661-99761797	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:99761577-99761888	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:99765773-99765873	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:99760728-99761052	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr7:99766722-99767140	HepG2	liver:	n/a	n/a
20	CHD2	chr7:99760749-99761065	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr7:99765514-99765792	K562	blood:	n/a	n/a
22	CHD2	chr7:99765776-99765849	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr7:99768813-99769072	A549	lung:	n/a	n/a
24	CTCF	chr7:99766500-99766650	HRE	kidney:	n/a	n/a
25	CTCF	chr7:99766561-99766647	GM12892	blood:	n/a	n/a
26	CTCF	chr7:99765920-99766070	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr7:99766120-99766270	BJ	skin:	n/a	n/a
28	CTCF	chr7:99766530-99766660	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr7:99766500-99766650	HPF	lung:	n/a	n/a
30	CTCF	chr7:99766060-99766210	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr7:99766460-99766610	HPF	lung:	n/a	n/a
32	CTCF	chr7:99766080-99766230	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr7:99766480-99766630	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr7:99766460-99766610	K562	blood:	n/a	n/a
35	CTCF	chr7:99766560-99766710	SAEC	small airway:	n/a	n/a
36	CTCF	chr7:99766460-99766610	BJ	skin:	n/a	n/a
37	CTCF	chr7:99766220-99766370	AG04450	lung:	n/a	n/a
38	CTCF	chr7:99766300-99766450	WI-38	lung:	n/a	n/a
39	CTCF	chr7:99766520-99766670	HCT-116	colon:	n/a	n/a
40	CTCF	chr7:99766480-99766630	AG09319	gingival:	n/a	n/a
41	CTCF	chr7:99766504-99766687	K562	blood:	n/a	n/a
42	CTCF	chr7:99766480-99766630	GM12864	blood:	n/a	n/a
43	CTCF	chr7:99766500-99766650	AG09319	gingival:	n/a	n/a
44	CTCF	chr7:99766520-99766670	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr7:99766480-99766630	HMF	breast:	n/a	n/a
46	CTCF	chr7:99766100-99766250	HPF	lung:	n/a	n/a
47	CTCF	chr7:99766391-99766430	GM20000	blood:	n/a	n/a
48	CTCF	chr7:99766500-99766650	HEK293	kidney:	n/a	n/a
49	CTCF	chr7:99766344-99766693	K562	blood:	n/a	n/a
50	CTCF	chr7:99765720-99765870	AG09319	gingival:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99765818-99765868	HEK293	kidney:	embryo
2	chr7:99765818-99765868	HEK293	kidney:	embryo
3	chr7:99757654-99757704	ProgFib	skin:	n/a
4	chr7:99769602-99769652	ProgFib	skin:	n/a
5	chr7:99766467-99766517	SK-N-MC	brain:	n/a
6	chr7:99769118-99769168	RPTEC	kidney:	n/a
7	chr7:99767134-99767184	AG10803	skin:	n/a
8	chr7:99766467-99766517	NB4	blood:	n/a
9	chr7:99767035-99767085	AG04450	lung:	fetal
10	chr7:99766467-99766517	AG10803	skin:	n/a
11	chr7:99769602-99769652	GM06990	blood:	n/a
12	chr7:99766376-99766426	NHDF-neo	bronchial:	n/a
13	chr7:99768028-99768078	SAEC	small airway:	n/a
14	chr7:99766376-99766426	SK-N-SH	brain:	n/a
15	chr7:99766655-99766705	HRPEpiC	eye:	n/a
16	chr7:99761767-99761817	A549	lung:	n/a
17	chr7:99766552-99766602	SK-N-MC	brain:	n/a
18	chr7:99757800-99757850	HRPEpiC	eye:	n/a
19	chr7:99765818-99765868	AG04449	skin:	fetal
20	chr7:99765818-99765868	GM19239	blood:	n/a
21	chr7:99768885-99768935	HCM	heart:	n/a
22	chr7:99766665-99766715	ECC-1	luminal epithelium:	n/a
23	chr7:99757654-99757704	GM06990	blood:	n/a
24	chr7:99766655-99766705	PFSK-1	brain:	n/a
25	chr7:99766655-99766705	HCM	heart:	n/a
26	chr7:99768028-99768078	BE2_C	brain:	n/a
27	chr7:99766552-99766602	HEEpiC	esophagus:	n/a
28	chr7:99765818-99765868	PFSK-1	brain:	n/a
29	chr7:99766655-99766705	PANC-1	pancreas:	n/a
30	chr7:99766467-99766517	HUVEC	blood vessel:	n/a
31	chr7:99761767-99761817	GM12891	blood:	n/a
32	chr7:99766203-99766253	HEEpiC	esophagus:	n/a
33	chr7:99761053-99761103	A549	lung:	n/a
34	chr7:99769432-99769482	AG04449	skin:	fetal
35	chr7:99769118-99769168	HL-60	blood:	n/a
36	chr7:99766665-99766715	ProgFib	skin:	n/a
37	chr7:99766203-99766253	ovcar-3	ovarian:	n/a
38	chr7:99768885-99768935	HCPEpiC	choroid plexus:	n/a
39	chr7:99767134-99767184	RPTEC	kidney:	n/a
40	chr7:99757654-99757704	NHDF-neo	bronchial:	n/a
41	chr7:99767134-99767184	HCT-116	colon:	n/a
42	chr7:99765818-99765868	GM12892	blood:	n/a
43	chr7:99769558-99769608	HCT-116	colon:	n/a
44	chr7:99769602-99769652	AG10803	skin:	n/a
45	chr7:99765818-99765868	AG09319	gingival:	n/a
46	chr7:99757654-99757704	SK-N-SH	brain:	n/a
47	chr7:99766655-99766705	AG04450	lung:	fetal
48	chr7:99757800-99757850	SKMC	muscle:	n/a
49	chr7:99766467-99766517	GM06990	blood:	n/a
50	chr7:99766376-99766426	Jurkat	blood:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99754403..99756202-chr7:99762627..99764486,3	K562	blood:
2	chr7:99722989..99725299-chr7:99765858..99767612,2	MCF-7	breast:
3	chr7:99754180..99757947-chr7:99773944..99778293,5	K562	blood:
4	chr7:99696142..99700081-chr7:99754300..99760427,7	MCF-7	breast:
5	chr7:99726058..99730231-chr7:99754511..99757895,5	MCF-7	breast:
6	chr7:99767104..99770027-chr7:99772999..99775636,2	MCF-7	breast:
7	chr7:99761601..99763212-chr7:99780948..99783504,2	K562	blood:
8	chr7:99754767..99758198-chr7:99759049..99763228,6	MCF-7	breast:
9	chr7:99760942..99762936-chr7:99767762..99771413,3	MCF-7	breast:
10	chr7:99749770..99752333-chr7:99765768..99768227,2	MCF-7	breast:
11	chr7:99760302..99763071-chr7:99770976..99773286,2	K562	blood:
12	chr7:99750795..99756202-chr7:99762627..99766634,7	K562	blood:
13	chr7:99759440..99762424-chr7:99762477..99764332,2	K562	blood:
14	chr7:99759206..99760844-chr7:99773976..99776568,2	MCF-7	breast:
15	chr7:99758106..99763245-chr7:99767736..99770623,4	K562	blood:
16	chr7:99752857..99757651-chr7:99763240..99770051,14	MCF-7	breast:
17	chr7:99764650..99767201-chr7:99768632..99771682,4	MCF-7	breast:
18	chr7:99759410..99761254-chr7:99763646..99766168,2	MCF-7	breast:
19	chr7:99760958..99763450-chr7:99810400..99812602,2	K562	blood:
20	chr7:99756435..99758861-chr7:99763048..99766609,5	K562	blood:
21	chr7:99752857..99757651-chr7:99763240..99770051,14	MCF-7	breast:
22	chr7:99688297..99690647-chr7:99759308..99762141,2	K562	blood:
23	chr7:99756236..99758894-chr7:100025899..100028598,2	K562	blood:
24	chr7:99753295..99755968-chr7:99764966..99767548,3	K562	blood:
25	chr7:99767272..99770756-chr7:99771153..99775151,5	MCF-7	breast:
26	chr7:99750253..99753026-chr7:99768043..99770127,2	MCF-7	breast:
27	chr7:99697328..99700192-chr7:99766386..99767944,2	MCF-7	breast:
28	chr6:150037573..150039874-chr7:99755624..99757771,2	MCF-7	breast:
29	chr7:99759295..99762077-chr7:100025040..100029116,3	MCF-7	breast:
30	chr7:99763454..99766181-chr7:99772749..99774869,2	K562	blood:
31	chr7:99767011..99769810-chr7:99997937..100000138,2	MCF-7	breast:
32	chr7:99755120..99757903-chr7:99766969..99769742,4	K562	blood:
33	chr7:99720651..99722811-chr7:99761432..99764330,2	K562	blood:
34	chr7:99696160..99700887-chr7:99753963..99757907,5	K562	blood:
35	chr7:99751690..99753574-chr7:99764837..99766531,2	MCF-7	breast:
36	chr7:99755258..99758996-chr7:99773394..99775783,3	MCF-7	breast:
37	chr7:99759440..99762424-chr7:99762477..99764332,2	K562	blood:
38	chr7:99765936..99768056-chr7:99933468..99935315,2	MCF-7	breast:
39	chr7:99724063..99726491-chr7:99755814..99759003,3	K562	blood:
40	chr7:99751463..99761050-chr7:99772463..99778676,10	K562	blood:
41	chr7:99762393..99763903-chr7:99796471..99799217,2	K562	blood:
42	chr7:99764650..99767201-chr7:99768632..99771682,4	MCF-7	breast:
43	chr7:99753966..99755669-chr7:99756075..99758782,2	MCF-7	breast:
44	chr7:99758919..99761962-chr7:99764565..99766487,3	K562	blood:
45	chr16:2906493..2908640-chr7:99756107..99758046,2	MCF-7	breast:
46	chr7:99696160..99699295-chr7:99753963..99757907,4	K562	blood:
47	chr7:99754473..99757305-chr7:99763282..99766035,2	MCF-7	breast:

No data

Variant related genes	Relation type
GAL3ST4	TF binding region
C7orf43	TF binding region
MIR4658	TF binding region
GAL3ST4	CpG island
C7orf43	CpG island
MIR4658	CpG island
ENSG00000263325	chromatin interactions
ENSG00000197093	chromatin interactions
ENSG00000066923	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000266154	chromatin interactions
ENSG00000146826	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000121716	chromatin interactions
ENSG00000005001	chromatin interactions
ENSG00000188186	chromatin interactions
ENSG00000214309	chromatin interactions
ENSG00000235077	chromatin interactions
ENSG00000242798	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000242294	chromatin interactions
ENSG00000131023	chromatin interactions
ENSG00000272752	chromatin interactions
ENSG00000213420	chromatin interactions
ENSG00000221838	chromatin interactions

Extended variants
information (count: 481 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550771073	chr7:99757472-99757473	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
2	rs568990471	chr7:99757482-99757483	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
3	rs530654612	chr7:99757486-99757487	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs551945117	chr7:99757506-99757507	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
5	rs368628642	chr7:99757535-99757536	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
6	rs371583641	chr7:99757549-99757550	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
7	rs141833027	chr7:99757553-99757554	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
8	rs150622786	chr7:99757587-99757588	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
9	rs374664217	chr7:99757591-99757592	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
10	rs139185482	chr7:99757594-99757595	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
11	rs149961692	chr7:99757598-99757599	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
12	rs201798961	chr7:99757601-99757602	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
13	rs3823646	chr7:99757612-99757613	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs140509773	chr7:99757641-99757642	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
15	rs144461733	chr7:99757654-99757655	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
16	rs150667953	chr7:99757655-99757656	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
17	rs13247092	chr7:99757674-99757675	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
18	rs576608275	chr7:99757679-99757680	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
19	rs201047364	chr7:99757685-99757686	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
20	rs557126552	chr7:99757690-99757691	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
21	rs200495131	chr7:99757693-99757694	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
22	rs546464217	chr7:99757698-99757699	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
23	rs113124394	chr7:99757701-99757702	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
24	rs111273114	chr7:99757705-99757706	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
25	rs142497803	chr7:99757712-99757713	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
26	rs13232713	chr7:99757721-99757722	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
27	rs13232718	chr7:99757727-99757728	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
28	rs199565529	chr7:99757738-99757739	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
29	rs200159207	chr7:99757739-99757740	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
30	rs375932821	chr7:99757744-99757745	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
31	rs573489011	chr7:99757746-99757747	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
32	rs150936564	chr7:99757783-99757784	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
33	rs267601670	chr7:99757800-99757801	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
34	rs543582140	chr7:99757801-99757802	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
35	rs141078471	chr7:99757807-99757808	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
36	rs540539176	chr7:99757811-99757812	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
37	rs13247241	chr7:99757812-99757813	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
38	rs145166071	chr7:99757813-99757814	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
39	rs138915937	chr7:99757830-99757831	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
40	rs200605076	chr7:99757852-99757853	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
41	rs376146452	chr7:99757860-99757861	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
42	rs544186969	chr7:99757873-99757874	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
43	rs140660995	chr7:99757888-99757889	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs145834509	chr7:99757889-99757890	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
45	rs369836654	chr7:99757901-99757902	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs149856343	chr7:99757911-99757912	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs373835115	chr7:99757912-99757913	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs533248969	chr7:99757924-99757925	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs551957728	chr7:99757933-99757934	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs570514466	chr7:99757934-99757935	Weak transcription Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	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
Gastric cancer	24379144	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
Prostate cancer	16461572	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
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1043 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99755600-99758400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:99756600-99760400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:99756600-99764200	Weak transcription	Spleen	Spleen
4	chr7:99756800-99758000	Enhancers	Primary T cells fromperipheralblood	blood
5	chr7:99756800-99758200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:99756800-99758200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:99756800-99758600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr7:99756800-99758600	Enhancers	Placenta	Placenta
9	chr7:99756800-99760600	Weak transcription	Colonic Mucosa	Colon
10	chr7:99756800-99760600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr7:99756800-99760800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr7:99756800-99764200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:99756800-99765200	Weak transcription	Right Atrium	heart
14	chr7:99756800-99765400	Weak transcription	Pancreas	Pancrea
15	chr7:99757000-99757600	Weak transcription	Fetal Stomach	stomach
16	chr7:99757000-99759000	Enhancers	K562	blood
17	chr7:99757000-99759400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:99757000-99759800	Weak transcription	Fetal Intestine Large	intestine
19	chr7:99757000-99760400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr7:99757000-99760400	Weak transcription	Fetal Intestine Small	intestine
21	chr7:99757000-99760400	Weak transcription	NHEK	skin
22	chr7:99757000-99760600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr7:99757000-99760600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr7:99757000-99760600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr7:99757000-99760600	Weak transcription	Primary B cells from cord blood	blood
26	chr7:99757000-99760600	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr7:99757000-99760600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr7:99757000-99760600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr7:99757000-99760600	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr7:99757000-99760600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr7:99757000-99760600	Weak transcription	Stomach Mucosa	stomach
32	chr7:99757000-99760600	Weak transcription	A549	lung
33	chr7:99757000-99760600	Weak transcription	GM12878-XiMat	blood
34	chr7:99757000-99761000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:99757000-99763800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:99757000-99763800	Weak transcription	Fetal Brain Female	brain
37	chr7:99757000-99764000	Weak transcription	Brain Hippocampus Middle	brain
38	chr7:99757000-99764000	Weak transcription	Fetal Lung	lung
39	chr7:99757000-99764600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:99757000-99764600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:99757000-99765000	Weak transcription	HSMM	muscle
42	chr7:99757000-99765400	Weak transcription	HSMMtube	muscle
43	chr7:99757200-99759200	Strong transcription	Fetal Thymus	thymus
44	chr7:99757200-99759600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr7:99757200-99759600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:99757200-99759800	Weak transcription	Primary T cells from cord blood	blood
47	chr7:99757200-99760400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:99757200-99760400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr7:99757200-99760400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:99757200-99760400	Weak transcription	Primary T helper cells PMA-I stimulated	--

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