Variant report

Variant	esv1850821
Chromosome Location	chr7:38378932-38411586
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2095)
CpG islands
(count:611)
Chromatin interactive
region (count:16)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2095 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

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	chr7:38389490-38389669	K562	blood:	n/a	n/a
3	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
4	ATF1	chr7:38380742-38381291	K562	blood:	n/a	n/a
5	ATF2	chr7:38409406-38409844	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:38409481-38409625	K562	blood:	n/a	n/a
7	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
8	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
9	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
10	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
11	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
12	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
13	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
14	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
15	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
16	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
17	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
18	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
19	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
20	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
21	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
22	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
23	BATF	chr7:38407600-38408059	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
25	BCL11A	chr7:38407578-38407819	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
27	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
28	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
31	BCLAF1	chr7:38407679-38408065	GM12878	blood:	n/a	n/a
32	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:38409538-38409840	K562	blood:	n/a	n/a
35	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
36	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:38407780-38408107	K562	blood:	n/a	n/a
38	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
39	BHLHE40	chr7:38407782-38408093	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:38409540-38409919	HepG2	liver:	n/a	n/a
43	BHLHE40	chr7:38380767-38381281	K562	blood:	n/a	n/a
44	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
45	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
46	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a
47	BHLHE40	chr7:38409415-38409953	GM12878	blood:	n/a	n/a
48	BRCA1	chr7:38408981-38409171	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr7:38409444-38409763	K562	blood:	n/a	n/a
50	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38408106-38408156	SK-N-SH	brain:	n/a
2	chr7:38408106-38408156	SK-N-SH	brain:	n/a
3	chr7:38403507-38403557	NHDF-neo	bronchial:	n/a
4	chr7:38389685-38389735	HEK293	kidney:	embryo
5	chr7:38380582-38380632	AG09309	skin:	n/a
6	chr7:38380582-38380632	AG09319	gingival:	n/a
7	chr7:38408106-38408156	SKMC	muscle:	n/a
8	chr7:38389659-38389709	HCPEpiC	choroid plexus:	n/a
9	chr7:38380582-38380632	K562	blood:	n/a
10	chr7:38409725-38409775	HEK293	kidney:	embryo
11	chr7:38389685-38389735	HRE	kidney:	n/a
12	chr7:38408106-38408156	HL-60	blood:	n/a
13	chr7:38380487-38380537	HIPEpiC	eye:	n/a
14	chr7:38408106-38408156	BJ	skin:	n/a
15	chr7:38408106-38408156	HRE	kidney:	n/a
16	chr7:38398839-38398889	HCF	heart:	n/a
17	chr7:38389659-38389709	AG10803	skin:	n/a
18	chr7:38380582-38380632	SKMC	muscle:	n/a
19	chr7:38389991-38390041	SK-N-SH_RA	brain:	n/a
20	chr7:38409725-38409775	AG09319	gingival:	n/a
21	chr7:38389991-38390041	AG09309	skin:	n/a
22	chr7:38398839-38398889	HAEpiC	amniotic membrane:	n/a
23	chr7:38380487-38380537	PrEC	prostate:	n/a
24	chr7:38398836-38398886	Hepatocyte	liver:	n/a
25	chr7:38398836-38398886	PrEC	prostate:	n/a
26	chr7:38389659-38389709	AG09319	gingival:	n/a
27	chr7:38380582-38380632	NHBE	bronchial:	n/a
28	chr7:38389659-38389709	NHDF-neo	bronchial:	n/a
29	chr7:38398839-38398889	NH-A	brain:	n/a
30	chr7:38389991-38390041	HRCEpiC	kidney:	n/a
31	chr7:38389685-38389735	NB4	blood:	n/a
32	chr7:38380487-38380537	K562	blood:	n/a
33	chr7:38398839-38398889	RPTEC	kidney:	n/a
34	chr7:38398836-38398886	GM19239	blood:	n/a
35	chr7:38380582-38380632	AoSMC	blood vessel:	n/a
36	chr7:38389991-38390041	HRPEpiC	eye:	n/a
37	chr7:38408106-38408156	NT2-D1	testis:	n/a
38	chr7:38380487-38380537	AG10803	skin:	n/a
39	chr7:38389991-38390041	CMK	blood:	n/a
40	chr7:38409725-38409775	SK-N-MC	brain:	n/a
41	chr7:38398839-38398889	Jurkat	blood:	n/a
42	chr7:38389991-38390041	SAEC	small airway:	n/a
43	chr7:38408106-38408156	U87	brain:	n/a
44	chr7:38380582-38380632	PFSK-1	brain:	n/a
45	chr7:38409725-38409775	NHDF-neo	bronchial:	n/a
46	chr7:38389991-38390041	Caco-2	colon:	n/a
47	chr7:38408106-38408156	HRCEpiC	kidney:	n/a
48	chr7:38409725-38409775	K562	blood:	n/a
49	chr7:38408106-38408156	GM12892	blood:	n/a
50	chr7:38408106-38408156	LNCaP	prostate:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
2	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
3	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
4	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
5	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
6	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
7	chr7:38269978..38272526-chr7:38377435..38379545,2	K562	blood:
8	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
9	chr7:38380741..38382401-chr7:38383649..38386131,2	K562	blood:
10	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
11	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
12	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
13	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
14	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
15	chr7:38409691..38411244-chr7:38417623..38419459,2	K562	blood:
16	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:

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

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

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
ENSG00000211697	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000211696	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211698	chromatin interactions
SERTAD3	miRNA target sites
RAB5A	miRNA target sites
CA13	miRNA target sites

Extended variants
information (count: 2040 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2040 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543859916	chr7:38378937-38378938	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs117685409	chr7:38378954-38378955	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs549566835	chr7:38378977-38378978	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs369276550	chr7:38379088-38379089	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs145090319	chr7:38379220-38379221	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs377221806	chr7:38379224-38379225	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs372157837	chr7:38379228-38379229	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs540499172	chr7:38379250-38379251	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs138946244	chr7:38379308-38379309	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs2735150	chr7:38379353-38379354	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546032059	chr7:38379364-38379365	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs34563781	chr7:38379369-38379370	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs565226910	chr7:38379372-38379373	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs531082932	chr7:38379376-38379377	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs567728580	chr7:38379377-38379378	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs6953358	chr7:38379379-38379380	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs59419447	chr7:38379380-38379381	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs550681479	chr7:38379432-38379433	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs567614153	chr7:38379433-38379434	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552533070	chr7:38379438-38379439	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs200812235	chr7:38379510-38379511	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs530055343	chr7:38379514-38379515	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs150742709	chr7:38379527-38379528	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs139119242	chr7:38379531-38379532	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs376801831	chr7:38379554-38379555	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs186244604	chr7:38379621-38379622	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs369158276	chr7:38379634-38379635	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs369719395	chr7:38379667-38379668	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs557129259	chr7:38379705-38379706	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs559151107	chr7:38379735-38379736	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs568837070	chr7:38379779-38379780	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs73355482	chr7:38379782-38379783	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs570440244	chr7:38379843-38379844	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	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
42	rs143879102	chr7:38380138-38380139	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs192051289	chr7:38380152-38380153	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs531418202	chr7:38380224-38380225	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs183596910	chr7:38380225-38380226	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs561048253	chr7:38380226-38380227	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs909158	chr7:38380230-38380231	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
48	rs374855004	chr7:38380251-38380252	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs546629253	chr7:38380296-38380297	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs566819623	chr7:38380332-38380333	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 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:1000 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	chr7:38377000-38379600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:38377000-38379800	Weak transcription	Primary T cells from cord blood	blood
32	chr7:38377400-38379000	Weak transcription	Dnd41	blood
33	chr7:38377400-38379800	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr7:38377400-38379800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr7:38377400-38379800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr7:38377400-38379800	Weak transcription	Fetal Intestine Small	intestine
37	chr7:38377400-38379800	Weak transcription	Fetal Thymus	thymus
38	chr7:38377400-38380000	Weak transcription	Pancreas	Pancrea
39	chr7:38377600-38379800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr7:38377600-38379800	Weak transcription	Fetal Intestine Large	intestine
41	chr7:38377600-38379800	Weak transcription	Placenta	Placenta
42	chr7:38377600-38379800	Active TSS	K562	blood
43	chr7:38378200-38379200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:38378200-38380000	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr7:38378200-38380200	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr7:38378800-38379800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr7:38378800-38380000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr7:38379000-38380400	Enhancers	Dnd41	blood
49	chr7:38379200-38381600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:38379600-38382000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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