Variant report

Variant	nsv915560
Chromosome Location	chr10:536704-816628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2572)
CpG islands
(count:17110)
Chromatin interactive
region (count:203)
LncRNA
region (count:24)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:2572 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:560158-560320	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:758256-758463	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:695549-696087	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:557055-557317	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:727897-728114	HepG2	liver:	n/a	n/a
6	ATF1	chr10:671105-671391	K562	blood:	n/a	n/a
7	ATF1	chr10:691655-691733	K562	blood:	n/a	n/a
8	ATF1	chr10:729319-729702	K562	blood:	n/a	n/a
9	ATF1	chr10:813001-813370	K562	blood:	n/a	n/a
10	ATF2	chr10:552845-553477	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr10:552889-553420	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr10:603849-604150	H1-hESC	embryonic stem cell:	n/a	chr10:603936-603945
13	ATF3	chr10:603843-604054	K562	blood:	n/a	chr10:603936-603945
14	BACH1	chr10:718041-718363	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr10:699656-699670	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr10:734911-735245	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:736069-736281	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr10:659440-659457	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr10:670408-671428	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr10:654721-654968	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr10:556959-557424	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr10:590435-590657	GM12878	blood:	n/a	n/a
23	BATF	chr10:722079-722448	GM12878	blood:	n/a	n/a
24	BATF	chr10:723859-724161	GM12878	blood:	n/a	n/a
25	BATF	chr10:705986-706335	GM12878	blood:	n/a	n/a
26	BATF	chr10:722135-722417	GM12878	blood:	n/a	n/a
27	BCL11A	chr10:811979-812582	GM12878	blood:	n/a	n/a
28	BCL11A	chr10:723812-724184	GM12878	blood:	n/a	chr10:723831-723839 chr10:724070-724079 chr10:723932-723945
29	BCL11A	chr10:722144-722453	GM12878	blood:	n/a	n/a
30	BCL11A	chr10:705958-706431	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:743024-743363	GM12878	blood:	n/a	chr10:743188-743197
32	BCL11A	chr10:769301-769535	GM12878	blood:	n/a	n/a
33	BCL11A	chr10:552994-553430	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL3	chr10:812586-812912	GM12878	blood:	n/a	n/a
35	BCL3	chr10:746085-746825	GM12878	blood:	n/a	n/a
36	BCL3	chr10:745959-746729	GM12878	blood:	n/a	n/a
37	BHLHE40	chr10:695707-696007	HepG2	liver:	n/a	n/a
38	BHLHE40	chr10:764330-764448	K562	blood:	n/a	n/a
39	BHLHE40	chr10:556974-557331	K562	blood:	n/a	chr10:557149-557165
40	BHLHE40	chr10:556973-557325	HepG2	liver:	n/a	chr10:557149-557165
41	BHLHE40	chr10:587767-588048	GM12878	blood:	n/a	n/a
42	BHLHE40	chr10:679292-679487	HepG2	liver:	n/a	n/a
43	BHLHE40	chr10:670986-671329	K562	blood:	n/a	n/a
44	BHLHE40	chr10:769085-769382	K562	blood:	n/a	n/a
45	BHLHE40	chr10:743220-743294	GM12878	blood:	n/a	n/a
46	BHLHE40	chr10:673571-673899	K562	blood:	n/a	n/a
47	BHLHE40	chr10:556971-557294	GM12878	blood:	n/a	chr10:557149-557165
48	BHLHE40	chr10:695485-697003	HepG2	liver:	n/a	n/a
49	BHLHE40	chr10:711494-711760	K562	blood:	n/a	chr10:711672-711681 chr10:711670-711683 chr10:711666-711687 chr10:711558-711571 chr10:711673-711682 chr10:711671-711680 chr10:711672-711681
50	BHLHE40	chr10:629787-629980	K562	blood:	n/a	chr10:629835-629844 chr10:629836-629845 chr10:629835-629844

(count:17110 , 50 per page) page: 1 2 3 4 5 6 7 ... 343

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:658638-658688	SK-N-MC	brain:	n/a
2	chr10:569006-569056	Hepatocyte	liver:	n/a
3	chr10:566129-566179	MCF-7	breast:	n/a
4	chr10:575899-575949	NB4	blood:	n/a
5	chr10:729001-729051	HUVEC	blood vessel:	n/a
6	chr10:677269-677319	GM12892	blood:	n/a
7	chr10:661388-661438	AG04450	lung:	fetal
8	chr10:557653-557703	HCT-116	colon:	n/a
9	chr10:665102-665152	HMEC	breast:	n/a
10	chr10:549040-549090	LNCaP	prostate:	n/a
11	chr10:577713-577763	NH-A	brain:	n/a
12	chr10:671497-671547	HMEC	breast:	n/a
13	chr10:653567-653617	PrEC	prostate:	n/a
14	chr10:667094-667144	SAEC	small airway:	n/a
15	chr10:766431-766481	HAEpiC	amniotic membrane:	n/a
16	chr10:630310-630360	PFSK-1	brain:	n/a
17	chr10:773141-773191	RPTEC	kidney:	n/a
18	chr10:709610-709660	SK-N-SH_RA	brain:	n/a
19	chr10:697901-697951	PrEC	prostate:	n/a
20	chr10:680352-680402	T-47D	breast:	n/a
21	chr10:773141-773191	HAEpiC	amniotic membrane:	n/a
22	chr10:547025-547075	HRE	kidney:	n/a
23	chr10:559468-559518	HCT-116	colon:	n/a
24	chr10:742727-742777	AG09309	skin:	n/a
25	chr10:682147-682197	IMR90	lung:	fetal
26	chr10:665510-665560	ProgFib	skin:	n/a
27	chr10:708425-708475	SK-N-SH	brain:	n/a
28	chr10:734268-734318	HEK293	kidney:	embryo
29	chr10:553457-553507	AG10803	skin:	n/a
30	chr10:729479-729529	PFSK-1	brain:	n/a
31	chr10:658638-658688	SK-N-MC	brain:	n/a
32	chr10:569006-569056	Hepatocyte	liver:	n/a
33	chr10:566129-566179	MCF-7	breast:	n/a
34	chr10:575899-575949	NB4	blood:	n/a
35	chr10:729001-729051	HUVEC	blood vessel:	n/a
36	chr10:677269-677319	GM12892	blood:	n/a
37	chr10:661388-661438	AG04450	lung:	fetal
38	chr10:557653-557703	HCT-116	colon:	n/a
39	chr10:665102-665152	HMEC	breast:	n/a
40	chr10:549040-549090	LNCaP	prostate:	n/a
41	chr10:577713-577763	NH-A	brain:	n/a
42	chr10:671497-671547	HMEC	breast:	n/a
43	chr10:653567-653617	PrEC	prostate:	n/a
44	chr10:667094-667144	SAEC	small airway:	n/a
45	chr10:766431-766481	HAEpiC	amniotic membrane:	n/a
46	chr10:630310-630360	PFSK-1	brain:	n/a
47	chr10:773141-773191	RPTEC	kidney:	n/a
48	chr10:709610-709660	SK-N-SH_RA	brain:	n/a
49	chr10:697901-697951	PrEC	prostate:	n/a
50	chr10:680352-680402	T-47D	breast:	n/a

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
2	chr10:661839..665872-chr10:667806..670448,3	MCF-7	breast:
3	chr10:584008..586633-chr10:587341..589161,2	MCF-7	breast:
4	chr10:582102..583966-chr10:587212..590042,3	K562	blood:
5	chr10:551731..554315-chr10:554873..557476,2	MCF-7	breast:
6	chr10:664349..666248-chr10:669018..671009,2	K562	blood:
7	chr10:657812..661599-chr10:664177..667928,5	MCF-7	breast:
8	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
9	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
10	chr10:678817..681667-chr10:734486..736272,2	MCF-7	breast:
11	chr10:556490..559348-chr10:561200..563635,4	MCF-7	breast:
12	chr10:668238..670614-chr10:674134..675871,2	K562	blood:
13	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
14	chr10:625995..627810-chr10:664687..667494,2	K562	blood:
15	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:
16	chr10:736326..739216-chr10:743425..745379,3	K562	blood:
17	chr10:663042..665972-chr10:666314..668656,3	K562	blood:
18	chr10:701409..702201-chr19:4341065..4341565,2	MCF-7	breast:
19	chr10:668740..670601-chr10:679784..682752,2	K562	blood:
20	chr10:757872..760729-chr10:776939..779568,2	MCF-7	breast:
21	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
22	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
23	chr10:632427..634199-chr10:639895..642783,2	K562	blood:
24	chr10:634195..634721-chr10:829974..830911,3	MCF-7	breast:
25	chr10:603209..605062-chr10:710188..713086,2	MCF-7	breast:
26	chr10:578987..580530-chr10:655147..657083,2	MCF-7	breast:
27	chr10:633910..634891-chr10:834953..835643,3	MCF-7	breast:
28	chr10:630264..632276-chr10:643488..645388,2	MCF-7	breast:
29	chr10:556626..557550-chr10:572468..573398,6	MCF-7	breast:
30	chr10:580078..582771-chr10:585483..587204,2	MCF-7	breast:
31	chr10:783561..786479-chr10:789093..790752,2	MCF-7	breast:
32	chr10:641312..643673-chr10:645720..648516,2	MCF-7	breast:
33	chr10:588040..589570-chr10:591232..593419,2	K562	blood:
34	chr10:658782..661387-chr10:662609..665554,4	MCF-7	breast:
35	chr10:585455..588115-chr10:589415..592524,3	MCF-7	breast:
36	chr10:556626..557550-chr10:572468..573398,6	MCF-7	breast:
37	chr10:733897..735933-chr10:814143..815828,2	MCF-7	breast:
38	chr10:555810..559181-chr10:734014..736581,3	MCF-7	breast:
39	chr10:561226..563645-chr10:565375..568269,2	K562	blood:
40	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
41	chr10:564005..566324-chr10:657951..660938,2	MCF-7	breast:
42	chr10:691751..694285-chr10:694356..695999,2	K562	blood:
43	chr10:674481..678808-chr10:734028..737251,4	MCF-7	breast:
44	chr10:678262..679765-chr10:686218..688304,2	MCF-7	breast:
45	chr10:651435..654848-chr10:734005..736513,4	MCF-7	breast:
46	chr10:565703..567575-chr10:571015..572923,2	MCF-7	breast:
47	chr10:556641..557560-chr10:835088..835885,2	K562	blood:
48	chr10:731969..737087-chr10:747564..751327,5	MCF-7	breast:
49	chr10:778218..778758-chr10:824666..825446,2	MCF-7	breast:
50	chr10:657490..661073-chr10:672939..677212,4	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf108-3	chr10:736183-736265	NONHSAT010870
2	lnc-C10orf108-3	chr10:737256-737679	NONHSAT010870
3	lnc-C10orf108-6	chr10:779932-779973	NONHSAT010872
4	lnc-C10orf108-1	chr10:696231-696382	NONHSAT010867
5	lnc-C10orf108-1	chr10:695888-696118	NONHSAT010867
6	lnc-C10orf108-6	chr10:780517-780898	NONHSAT010872
7	lnc-C10orf108-1	chr10:707966-708058	NR_027152
8	lnc-LARP4B-3	chr10:724715-724736	NONHSAT010869
9	lnc-C10orf108-2	chr10:675799-676319	NONHSAT010863
10	lnc-C10orf108-4	chr10:790517-790898	XLOC_008335
11	lnc-C10orf108-3	chr10:737257-737679	XLOC_008334
12	lnc-C10orf108-4	chr10:789932-789973	XLOC_008335
13	lnc-LARP4B-3	chr10:724395-724591	NONHSAT010869
14	lnc-C10orf108-1	chr10:709498-709642	ENSG00000242357.1
15	lnc-C10orf108-3	chr10:736184-736265	XLOC_008334
16	lnc-C10orf108-1	chr10:697051-698595	NONHSAT010867
17	lnc-C10orf108-2	chr10:676345-677195	NONHSAT010863
18	lnc-C10orf108-2	chr10:675799-677195	ENSG00000225140.1
19	lnc-C10orf108-1	chr10:708731-711109	NR_027152
20	lnc-C10orf108-2	chr10:674578-674837	NONHSAT010863
21	lnc-C10orf108-2	chr10:674578-674837	ENSG00000225140.1
22	lnc-C10orf108-1	chr10:712158-712562	ENSG00000242357.1
23	lnc-C10orf108-5	chr10:714400-715521	ENSG00000272992.1
24	lnc-C10orf108-1	chr10:696017-696382	NR_027152

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5699-5p	chr10:687688-687709	MIMAT0027103
hsa-miR-5699-3p	chr10:687639-687660	MIMAT0022492

No data

Variant related genes	Relation type
MIR5699	TF binding region
PRR26	TF binding region
ENSG00000231601	TF binding region
ENSG00000242357	TF binding region
DIP2C	TF binding region
ENSG00000225140	TF binding region
ENSG00000272992	TF binding region
MIR5699	CpG island
PRR26	CpG island
ENSG00000231601	CpG island
ENSG00000242357	CpG island
DIP2C	CpG island
ENSG00000225140	CpG island
ENSG00000272992	CpG island
ENSG00000151240	chromatin interactions
ENSG00000231601	chromatin interactions
ENSG00000233021	chromatin interactions
ENSG00000047056	chromatin interactions
ENSG00000180525	chromatin interactions
ENSG00000225140	chromatin interactions
ENSG00000263511	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000272992	chromatin interactions
SEC24A	miRNA target sites
PTGS2	miRNA target sites
SEC23IP	miRNA target sites
PTK2	miRNA target sites

Extended variants
information (count: 15023 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:15023 , 50 per page) page: 1 2 3 4 5 6 7 ... 301

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529286843	chr10:536707-536708	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs553583162	chr10:536715-536716	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs368119357	chr10:536725-536726	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs182000349	chr10:536736-536737	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545904335	chr10:536740-536741	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs138170884	chr10:536743-536744	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs531346728	chr10:536787-536788	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs149560919	chr10:536808-536809	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs562385065	chr10:536814-536815	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs186234391	chr10:536824-536825	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs565816461	chr10:536841-536842	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs190243028	chr10:536849-536850	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs146287206	chr10:536852-536853	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs549153126	chr10:536889-536890	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs181495192	chr10:536912-536913	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs186615763	chr10:536966-536967	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs535841826	chr10:536968-536969	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs555503002	chr10:536981-536982	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs558791905	chr10:537000-537001	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs144371121	chr10:537010-537011	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs17293419	chr10:537014-537015	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533848848	chr10:537018-537019	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs553521685	chr10:537033-537034	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576630566	chr10:537045-537046	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs536704396	chr10:537098-537099	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs368690494	chr10:537119-537120	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs545539038	chr10:537130-537131	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs114933100	chr10:537139-537140	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs539465373	chr10:537149-537150	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs576085799	chr10:537154-537155	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs372302406	chr10:537163-537164	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs556651515	chr10:537190-537191	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs541794344	chr10:537203-537204	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs151236631	chr10:537218-537219	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs375842439	chr10:537238-537239	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs139416129	chr10:537286-537287	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs142625260	chr10:537293-537294	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs117644139	chr10:537308-537309	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs116580010	chr10:537362-537363	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs533558780	chr10:537393-537394	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs550157388	chr10:537406-537407	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs563777734	chr10:537407-537408	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs79064938	chr10:537411-537412	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs143613315	chr10:537417-537418	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs146004621	chr10:537434-537435	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs182595121	chr10:537443-537444	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs565760269	chr10:537477-537478	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs148657019	chr10:537485-537486	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs185447702	chr10:537493-537494	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs570453916	chr10:537495-537496	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:7293 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:517000-536800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:531200-536800	Weak transcription	Fetal Intestine Large	intestine
3	chr10:531400-536800	Weak transcription	Esophagus	oesophagus
4	chr10:531400-545800	Weak transcription	Gastric	stomach
5	chr10:531600-537000	Weak transcription	HSMMtube	muscle
6	chr10:531600-537400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr10:531600-540400	Enhancers	Brain Substantia Nigra	brain
8	chr10:532000-536800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr10:532000-544400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr10:532000-557000	Weak transcription	Pancreas	Pancrea
11	chr10:532600-536800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr10:532600-536800	Weak transcription	NH-A	brain
13	chr10:532600-540400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr10:532800-543200	Weak transcription	Fetal Intestine Small	intestine
15	chr10:533200-537000	Weak transcription	Fetal Brain Female	brain
16	chr10:533200-538200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr10:533200-539200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:533400-537000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr10:533400-539000	Weak transcription	Fetal Thymus	thymus
20	chr10:534000-536800	Enhancers	Brain Anterior Caudate	brain
21	chr10:534400-539200	Enhancers	Left Ventricle	heart
22	chr10:534400-540400	Enhancers	Fetal Muscle Trunk	muscle
23	chr10:534600-536800	Enhancers	Brain Cingulate Gyrus	brain
24	chr10:534600-536800	Enhancers	Rectal Smooth Muscle	rectum
25	chr10:534600-537000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr10:534600-537800	Enhancers	Right Atrium	heart
27	chr10:534600-541200	Enhancers	Brain Angular Gyrus	brain
28	chr10:534600-541400	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr10:534800-537000	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr10:535000-541200	Enhancers	Fetal Muscle Leg	muscle
31	chr10:535400-537000	Enhancers	Adipose Nuclei	Adipose
32	chr10:535600-536800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr10:535600-537000	Weak transcription	Lung	lung
34	chr10:535600-537400	Weak transcription	Aorta	Aorta
35	chr10:536000-537600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr10:536000-537800	Flanking Active TSS	Stomach Smooth Muscle	stomach
37	chr10:536000-539600	Enhancers	Colon Smooth Muscle	Colon
38	chr10:536000-541000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr10:536000-542000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr10:536200-536800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr10:536200-536800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr10:536200-537000	Enhancers	NHLF	lung
43	chr10:536200-537400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr10:536200-537600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:536200-537600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr10:536200-537600	Enhancers	Placenta	Placenta
47	chr10:536200-537600	Enhancers	HSMM	muscle
48	chr10:536200-537600	Flanking Active TSS	NHDF-Ad	bronchial
49	chr10:536200-537600	Flanking Active TSS	Osteobl	bone
50	chr10:536200-537800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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