Variant report

Variant	esv1847734
Chromosome Location	chr7:38379798-38408244
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1865)
CpG islands
(count:550)
Chromatin interactive
region (count:14)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1865 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38380924-38381236	K562	blood:	n/a	n/a
2	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
3	ATF1	chr7:38380742-38381291	K562	blood:	n/a	n/a
4	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
5	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
6	BATF	chr7:38407600-38408059	GM12878	blood:	n/a	n/a
7	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
8	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
9	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
10	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
11	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
12	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
13	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
14	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
15	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
16	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
17	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
18	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
19	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
20	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
21	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
24	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:38407578-38407819	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
27	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
28	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
29	BCLAF1	chr7:38407679-38408065	GM12878	blood:	n/a	n/a
30	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
31	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a
34	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
36	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
37	BHLHE40	chr7:38407780-38408107	K562	blood:	n/a	n/a
38	BHLHE40	chr7:38380767-38381281	K562	blood:	n/a	n/a
39	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
41	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
42	BHLHE40	chr7:38407782-38408093	GM12878	blood:	n/a	n/a
43	CBX3	chr7:38407677-38408137	K562	blood:	n/a	n/a
44	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
45	CBX3	chr7:38380820-38381270	K562	blood:	n/a	n/a
46	CBX3	chr7:38380733-38381387	K562	blood:	n/a	n/a
47	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
48	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
49	CBX3	chr7:38407763-38408208	HCT-116	colon:	n/a	n/a
50	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38380582-38380632	Hela-S3	cervix:	n/a
2	chr7:38380582-38380632	Hela-S3	cervix:	n/a
3	chr7:38398839-38398889	SK-N-SH_RA	brain:	n/a
4	chr7:38389685-38389735	HCF	heart:	n/a
5	chr7:38380582-38380632	HEEpiC	esophagus:	n/a
6	chr7:38408106-38408156	Hepatocyte	liver:	n/a
7	chr7:38389685-38389735	GM06990	blood:	n/a
8	chr7:38398836-38398886	MCF10A-Er-Src	breast:	n/a
9	chr7:38398839-38398889	GM19239	blood:	n/a
10	chr7:38398836-38398886	BJ	skin:	n/a
11	chr7:38403507-38403557	HIPEpiC	eye:	n/a
12	chr7:38398839-38398889	NHBE	bronchial:	n/a
13	chr7:38389991-38390041	SAEC	small airway:	n/a
14	chr7:38398839-38398889	BJ	skin:	n/a
15	chr7:38403507-38403557	SK-N-SH	brain:	n/a
16	chr7:38398839-38398889	MCF-7	breast:	n/a
17	chr7:38408106-38408156	Caco-2	colon:	n/a
18	chr7:38380487-38380537	SKMC	muscle:	n/a
19	chr7:38380487-38380537	HCT-116	colon:	n/a
20	chr7:38389991-38390041	HCPEpiC	choroid plexus:	n/a
21	chr7:38398839-38398889	HUVEC	blood vessel:	n/a
22	chr7:38389685-38389735	HCPEpiC	choroid plexus:	n/a
23	chr7:38380582-38380632	Caco-2	colon:	n/a
24	chr7:38408106-38408156	HRCEpiC	kidney:	n/a
25	chr7:38403507-38403557	A549	lung:	n/a
26	chr7:38389659-38389709	SKMC	muscle:	n/a
27	chr7:38389685-38389735	PANC-1	pancreas:	n/a
28	chr7:38403507-38403557	AG10803	skin:	n/a
29	chr7:38389659-38389709	LNCaP	prostate:	n/a
30	chr7:38380582-38380632	GM06990	blood:	n/a
31	chr7:38408106-38408156	AG09309	skin:	n/a
32	chr7:38389991-38390041	NHDF-neo	bronchial:	n/a
33	chr7:38380487-38380537	ECC-1	luminal epithelium:	n/a
34	chr7:38380487-38380537	SAEC	small airway:	n/a
35	chr7:38403507-38403557	PFSK-1	brain:	n/a
36	chr7:38403507-38403557	AG04449	skin:	fetal
37	chr7:38389659-38389709	U87	brain:	n/a
38	chr7:38389991-38390041	A549	lung:	n/a
39	chr7:38389991-38390041	BE2_C	brain:	n/a
40	chr7:38380582-38380632	NHDF-neo	bronchial:	n/a
41	chr7:38398839-38398889	AG09319	gingival:	n/a
42	chr7:38389685-38389735	HCM	heart:	n/a
43	chr7:38380487-38380537	HCF	heart:	n/a
44	chr7:38408106-38408156	H1-hESC	embryonic stem cell:	embryo
45	chr7:38380487-38380537	NB4	blood:	n/a
46	chr7:38398839-38398889	GM06990	blood:	n/a
47	chr7:38398836-38398886	BE2_C	brain:	n/a
48	chr7:38408106-38408156	AG04449	skin:	fetal
49	chr7:38380487-38380537	IMR90	lung:	fetal
50	chr7:38403507-38403557	HepG2	liver:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
2	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
3	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
4	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
5	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
6	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
7	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
8	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
9	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
10	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
11	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
12	chr7:38380741..38382401-chr7:38383649..38386131,2	K562	blood:
13	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
14	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-1	chr7:38381216-38381400	ENSG00000250924
2	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
3	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
4	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
5	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
6	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
7	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
8	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
9	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
10	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
11	lnc-AMPH-1	chr7:38407614-38407746	XLOC_006412
12	lnc-AMPH-1	chr7:38407246-38407494	XLOC_006412
13	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
14	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1
15	lnc-STARD3NL-1	chr7:38381178-38381400	NONHSAT120179
16	lnc-STARD3NL-1	chr7:38381098-38381400	NONHSAT120178
17	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
18	lnc-STARD3NL-1	chr7:38381747-38382154	NONHSAT120178

No data

Variant related genes	Relation type
TRGV7	TF binding region
TRGV5	TF binding region
TRGV1	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV2	TF binding region
TRGV5P	TF binding region
TRGV7	CpG island
TRGV5	CpG island
TRGV1	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV2	CpG island
TRGV5P	CpG island
ENSG00000211696	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000211698	chromatin interactions
SERTAD3	miRNA target sites
RAB5A	miRNA target sites
CA13	miRNA target sites

Extended variants
information (count: 1876 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1876 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570440244	chr7:38379843-38379844	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs554383857	chr7:38379854-38379855	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs78098272	chr7:38379858-38379859	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs574458909	chr7:38379860-38379861	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs137900436	chr7:38379905-38379906	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs149445913	chr7:38379923-38379924	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs34359157	chr7:38379952-38379953	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs553015710	chr7:38380092-38380093	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs2735149	chr7:38380135-38380136	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs143879102	chr7:38380138-38380139	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs192051289	chr7:38380152-38380153	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs531418202	chr7:38380224-38380225	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs183596910	chr7:38380225-38380226	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs561048253	chr7:38380226-38380227	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs909158	chr7:38380230-38380231	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
16	rs374855004	chr7:38380251-38380252	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs546629253	chr7:38380296-38380297	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs566819623	chr7:38380332-38380333	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs148682138	chr7:38380348-38380349	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs144542008	chr7:38380356-38380357	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs569399945	chr7:38380382-38380383	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs538078804	chr7:38380386-38380387	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs554603648	chr7:38380397-38380398	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs386712318	chr7:38380446-38380447	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs909157	chr7:38380447-38380448	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs61739334	chr7:38380487-38380488	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs147857203	chr7:38380488-38380489	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs539759334	chr7:38380500-38380501	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs139645452	chr7:38380582-38380583	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs576137693	chr7:38380584-38380585	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs541666905	chr7:38380608-38380609	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs561036038	chr7:38380612-38380613	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs188432089	chr7:38380617-38380618	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs537138953	chr7:38380624-38380625	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs540211266	chr7:38380626-38380627	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs560148472	chr7:38380644-38380645	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs373110101	chr7:38380695-38380696	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs112314082	chr7:38380753-38380754	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs375633957	chr7:38380759-38380760	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs375833599	chr7:38380765-38380766	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs532410973	chr7:38380771-38380772	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs552789869	chr7:38380788-38380789	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs113173577	chr7:38380806-38380807	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs576805790	chr7:38380819-38380820	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs535199904	chr7:38380828-38380829	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs192854511	chr7:38380846-38380847	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs548833651	chr7:38380851-38380852	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs568137545	chr7:38380913-38380914	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs575785942	chr7:38380932-38380933	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs533919599	chr7:38380939-38380940	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:875 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38371800-38380600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:38375400-38380800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:38375600-38380000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr7:38375600-38380000	Weak transcription	Spleen	Spleen
5	chr7:38375800-38379800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr7:38375800-38380000	Weak transcription	Fetal Muscle Trunk	muscle
7	chr7:38375800-38380400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:38375800-38380400	Weak transcription	A549	lung
9	chr7:38375800-38380800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:38375800-38380800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr7:38375800-38380800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:38375800-38380800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:38376000-38379800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr7:38376000-38379800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:38376000-38380000	Weak transcription	Fetal Stomach	stomach
16	chr7:38376000-38380400	Weak transcription	Fetal Muscle Leg	muscle
17	chr7:38376000-38380400	Weak transcription	Thymus	Thymus
18	chr7:38376000-38380400	Weak transcription	GM12878-XiMat	blood
19	chr7:38376000-38380600	Weak transcription	Adipose Nuclei	Adipose
20	chr7:38376200-38379800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr7:38376400-38379800	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr7:38376400-38379800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr7:38376400-38380600	Weak transcription	Primary B cells from cord blood	blood
24	chr7:38376400-38381000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr7:38376600-38379800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr7:38376600-38380000	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr7:38376600-38380600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr7:38376800-38379800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:38376800-38380800	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr7:38377000-38379800	Weak transcription	Primary T cells from cord blood	blood
31	chr7:38377400-38379800	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr7:38377400-38379800	Weak transcription	Primary hematopoietic stem cells	blood
33	chr7:38377400-38379800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr7:38377400-38379800	Weak transcription	Fetal Intestine Small	intestine
35	chr7:38377400-38379800	Weak transcription	Fetal Thymus	thymus
36	chr7:38377400-38380000	Weak transcription	Pancreas	Pancrea
37	chr7:38377600-38379800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr7:38377600-38379800	Weak transcription	Fetal Intestine Large	intestine
39	chr7:38377600-38379800	Weak transcription	Placenta	Placenta
40	chr7:38377600-38379800	Active TSS	K562	blood
41	chr7:38378200-38380000	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr7:38378200-38380200	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr7:38378800-38379800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr7:38378800-38380000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr7:38379000-38380400	Enhancers	Dnd41	blood
46	chr7:38379200-38381600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr7:38379600-38382000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:38379800-38380000	Active TSS	Primary T cells fromperipheralblood	blood
49	chr7:38379800-38380400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:38379800-38380400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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