Variant report

Variant	nsv1018193
Chromosome Location	chr6:167491589-167797294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5379)
CpG islands
(count:9287)
Chromatin interactive
region (count:82)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5379 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167554236-167555094	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167544586-167544925	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
20	ARID3A	chr6:167536241-167537214	HepG2	liver:	n/a	n/a
21	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
22	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
23	ATF1	chr6:167513659-167514463	K562	blood:	n/a	n/a
24	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
25	ATF1	chr6:167538302-167538600	K562	blood:	n/a	n/a
26	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
27	ATF2	chr6:167493214-167493693	GM12878	blood:	n/a	n/a
28	ATF2	chr6:167507302-167509165	GM12878	blood:	n/a	n/a
29	ATF2	chr6:167543402-167543914	GM12878	blood:	n/a	n/a
30	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr6:167576782-167577257	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr6:167502680-167503061	GM12878	blood:	n/a	n/a
33	ATF2	chr6:167566160-167566818	GM12878	blood:	n/a	n/a
34	ATF2	chr6:167516544-167517232	GM12878	blood:	n/a	n/a
35	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
36	ATF2	chr6:167526259-167528702	GM12878	blood:	n/a	chr6:167528159-167528170
37	ATF2	chr6:167512312-167512817	GM12878	blood:	n/a	n/a
38	ATF2	chr6:167560330-167560930	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr6:167526348-167528528	GM12878	blood:	n/a	chr6:167528159-167528170
41	ATF2	chr6:167564501-167565096	GM12878	blood:	n/a	n/a
42	ATF2	chr6:167493157-167493811	GM12878	blood:	n/a	n/a
43	ATF2	chr6:167560274-167560920	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr6:167531955-167532665	GM12878	blood:	n/a	n/a
45	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
46	ATF2	chr6:167506741-167509310	GM12878	blood:	n/a	n/a
47	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
48	ATF2	chr6:167564561-167565094	H1-hESC	embryonic stem cell:	n/a	n/a
49	ATF2	chr6:167566874-167567462	GM12878	blood:	n/a	n/a
50	ATF2	chr6:167566134-167567505	GM12878	blood:	n/a	n/a

(count:9287 , 50 per page) page: 1 2 3 4 5 6 7 ... 186

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167550181-167550231	NT2-D1	testis:	n/a
2	chr6:167705253-167705303	HEEpiC	esophagus:	n/a
3	chr6:167632873-167632923	AG04450	lung:	fetal
4	chr6:167794374-167794424	IMR90	lung:	fetal
5	chr6:167507762-167507812	HCT-116	colon:	n/a
6	chr6:167560504-167560554	NHBE	bronchial:	n/a
7	chr6:167700000-167700050	PrEC	prostate:	n/a
8	chr6:167763320-167763370	AoSMC	blood vessel:	n/a
9	chr6:167653907-167653957	AG04450	lung:	fetal
10	chr6:167680455-167680505	Hepatocyte	liver:	n/a
11	chr6:167571328-167571378	PFSK-1	brain:	n/a
12	chr6:167789539-167789589	MCF10A-Er-Src	breast:	n/a
13	chr6:167584201-167584251	BJ	skin:	n/a
14	chr6:167523797-167523847	HCT-116	colon:	n/a
15	chr6:167710360-167710410	NT2-D1	testis:	n/a
16	chr6:167550181-167550231	NT2-D1	testis:	n/a
17	chr6:167705253-167705303	HEEpiC	esophagus:	n/a
18	chr6:167632873-167632923	AG04450	lung:	fetal
19	chr6:167794374-167794424	IMR90	lung:	fetal
20	chr6:167507762-167507812	HCT-116	colon:	n/a
21	chr6:167560504-167560554	NHBE	bronchial:	n/a
22	chr6:167700000-167700050	PrEC	prostate:	n/a
23	chr6:167763320-167763370	AoSMC	blood vessel:	n/a
24	chr6:167653907-167653957	AG04450	lung:	fetal
25	chr6:167680455-167680505	Hepatocyte	liver:	n/a
26	chr6:167571328-167571378	PFSK-1	brain:	n/a
27	chr6:167789539-167789589	MCF10A-Er-Src	breast:	n/a
28	chr6:167584201-167584251	BJ	skin:	n/a
29	chr6:167523797-167523847	HCT-116	colon:	n/a
30	chr6:167710360-167710410	NT2-D1	testis:	n/a
31	chr6:167595418-167595468	HCF	heart:	n/a
32	chr6:167789441-167789491	NH-A	brain:	n/a
33	chr6:167560504-167560554	CMK	blood:	n/a
34	chr6:167791153-167791203	PrEC	prostate:	n/a
35	chr6:167631788-167631838	RPTEC	kidney:	n/a
36	chr6:167734054-167734104	GM19239	blood:	n/a
37	chr6:167508053-167508103	HIPEpiC	eye:	n/a
38	chr6:167649384-167649434	RPTEC	kidney:	n/a
39	chr6:167524115-167524165	HMEC	breast:	n/a
40	chr6:167704188-167704238	HCF	heart:	n/a
41	chr6:167738594-167738644	Jurkat	blood:	n/a
42	chr6:167587558-167587608	ProgFib	skin:	n/a
43	chr6:167571584-167571634	ProgFib	skin:	n/a
44	chr6:167695026-167695076	NHBE	bronchial:	n/a
45	chr6:167508191-167508241	Caco-2	colon:	n/a
46	chr6:167789195-167789245	GM12891	blood:	n/a
47	chr6:167530253-167530303	AG10803	skin:	n/a
48	chr6:167765110-167765160	SKMC	muscle:	n/a
49	chr6:167734054-167734104	NHDF-neo	bronchial:	n/a
50	chr6:167524115-167524165	HNPCEpiC	eye:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
2	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
3	chr6:167533925..167534442-chr6:167554372..167555227,2	MCF-7	breast:
4	chr6:167511835..167514028-chr6:167517104..167518840,2	K562	blood:
5	chr6:167514455..167516810-chr6:167518589..167520872,3	K562	blood:
6	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
7	chr6:167511835..167514028-chr6:167517104..167518840,2	K562	blood:
8	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
9	chr6:167573482..167576354-chr6:167702662..167705429,2	K562	blood:
10	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
11	chr6:167508063..167510526-chr6:167511244..167513696,2	K562	blood:
12	chr6:167186547..167188661-chr6:167553295..167555799,2	K562	blood:
13	chr6:167514002..167514845-chr6:167533614..167534539,2	MCF-7	breast:
14	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
15	chr6:167530846..167533349-chr6:167533846..167535491,2	K562	blood:
16	chr6:167533318..167534107-chr6:167555281..167555885,2	MCF-7	breast:
17	chr6:167514528..167517115-chr6:167518866..167520880,2	MCF-7	breast:
18	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
19	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
20	chr6:167508063..167510526-chr6:167511244..167513696,2	K562	blood:
21	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
22	chr6:167543795..167547055-chr6:167549259..167552787,3	K562	blood:
23	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
24	chr6:167547071..167549495-chr6:167560421..167562886,2	K562	blood:
25	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
26	chr6:167185783..167186302-chr6:167555369..167556350,2	K562	blood:
27	chr6:167550499..167553471-chr6:167563406..167565855,2	K562	blood:
28	chr6:167182263..167184637-chr6:167557115..167559460,2	K562	blood:
29	chr6:167516694..167518621-chr6:167521648..167524357,2	K562	blood:
30	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
31	chr6:167536255..167537788-chr6:167539934..167541454,2	K562	blood:
32	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
33	chr6:167188403..167189352-chr6:167555280..167555897,4	K562	blood:
34	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
35	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
36	chr6:167513997..167514603-chr6:167533661..167534449,3	MCF-7	breast:
37	chr6:167550499..167553471-chr6:167563406..167565855,2	K562	blood:
38	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
39	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
40	chr6:167530846..167533349-chr6:167533846..167535491,2	K562	blood:
41	chr6:167519100..167521232-chr6:167535131..167537207,2	K562	blood:
42	chr6:167559575..167562153-chr6:167565310..167566996,3	K562	blood:
43	chr6:167513997..167514603-chr6:167533661..167534449,3	MCF-7	breast:
44	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
45	chr6:167515250..167516810-chr6:167519372..167521331,2	K562	blood:
46	chr6:167530415..167533348-chr6:167542772..167545436,2	K562	blood:
47	chr6:167533318..167534107-chr6:167555281..167555885,2	MCF-7	breast:
48	chr6:167200031..167200812-chr6:167555407..167555996,2	K562	blood:
49	chr6:167188755..167189454-chr6:167555413..167556221,2	MCF-7	breast:
50	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCR6-2	chr6:167590485-167590622	NONHSAT116087
2	lnc-CCR6-2	chr6:167591872-167592248	NONHSAT116087
3	lnc-GPR31-3	chr6:167582786-167583124	NONHSAT116085
4	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
5	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
6	lnc-CCR6-2	chr6:167584146-167584210	NONHSAT116086
7	lnc-GPR31-2	chr6:167573626-167573961	l_3324_chr6:167571212-167573961_ovary
8	lnc-TCP10L2-1	chr6:167578697-167578796	NONHSAT116082
9	lnc-GPR31-3	chr6:167583147-167583385	FPKM1_group_28907_transcript_1
10	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
11	lnc-CCR6-2	chr6:167585632-167586297	NONHSAT116086
12	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
13	lnc-CCR6-1	chr6:167579265-167579394	NONHSAT116084
14	lnc-GPR31-3	chr6:167582786-167583034	FPKM1_group_28907_transcript_1
15	lnc-TCP10L2-1	chr6:167559902-167560143	NONHSAT116082
16	lnc-GPR31-3	chr6:167583039-167583124	FPKM1_group_28907_transcript_1
17	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
18	lnc-GPR31-3	chr6:167583147-167583385	NONHSAT116085
19	lnc-GPR31-2	chr6:167571213-167571283	l_3324_chr6:167571212-167573961_ovary
20	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
21	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
22	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
23	lnc-GPR31-5	chr6:167509671-167510205	NONHSAT116081
24	lnc-CCR6-2	chr6:167584159-167584210	NONHSAT116087
25	lnc-CCR6-1	chr6:167575369-167575443	NONHSAT116084
26	lnc-TCP10L2-1	chr6:167577889-167578048	NONHSAT116082
27	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
28	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097
29	lnc-TCP10L2-1	chr6:167562878-167562972	NONHSAT116082
30	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921

No data

Variant related genes	Relation type
UNC93A	TF binding region
TCP10	TF binding region
ENSG00000228648	TF binding region
TTLL2	TF binding region
CCR6	TF binding region
ENSG00000231720	TF binding region
GPR31	TF binding region
ENSG00000216966	TF binding region
TCP10L2	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TCP10	CpG island
ENSG00000228648	CpG island
TTLL2	CpG island
CCR6	CpG island
ENSG00000231720	CpG island
GPR31	CpG island
ENSG00000216966	CpG island
TCP10L2	CpG island
ENSG00000217447	CpG island
ENSG00000216966	chromatin interactions
ENSG00000112494	chromatin interactions
ENSG00000265828	chromatin interactions
ENSG00000166984	chromatin interactions
ENSG00000120436	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000112486	chromatin interactions
CYB5R4	miRNA target sites
CYBASC3	miRNA target sites

Extended variants
information (count: 13341 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:13341 , 50 per page) page: 1 2 3 4 5 6 7 ... 267

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4710176	chr6:167491639-167491640	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139258420	chr6:167491651-167491652	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs185273087	chr6:167491663-167491664	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs76004164	chr6:167491669-167491670	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs566831876	chr6:167491711-167491712	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs534187272	chr6:167491717-167491718	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs555362613	chr6:167491723-167491724	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs562440912	chr6:167491767-167491768	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs59034391	chr6:167491789-167491790	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs529695698	chr6:167491826-167491827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149970965	chr6:167491837-167491838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556380697	chr6:167491838-167491839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578012303	chr6:167491873-167491874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545690387	chr6:167491900-167491901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564275107	chr6:167491941-167491942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192002247	chr6:167491948-167491949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184196905	chr6:167491965-167491966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146762190	chr6:167491987-167491988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559687258	chr6:167492004-167492005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528885228	chr6:167492010-167492011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140377265	chr6:167492073-167492074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568861497	chr6:167492135-167492136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188676759	chr6:167492166-167492167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181037626	chr6:167492195-167492196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566695588	chr6:167492233-167492234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146494358	chr6:167492251-167492252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149084916	chr6:167492254-167492255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76103966	chr6:167492266-167492267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537856859	chr6:167492287-167492288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556482478	chr6:167492423-167492424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533577309	chr6:167492451-167492452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs9459867	chr6:167492509-167492510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558015106	chr6:167492532-167492533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555311625	chr6:167492533-167492534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540570726	chr6:167492551-167492552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7757618	chr6:167492552-167492553	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs184413841	chr6:167492566-167492567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543872651	chr6:167492600-167492601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190502728	chr6:167492605-167492606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532906610	chr6:167492616-167492617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182470768	chr6:167492723-167492724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148210148	chr6:167492727-167492728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527876435	chr6:167492743-167492744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549120118	chr6:167492762-167492763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73787910	chr6:167492775-167492776	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538498478	chr6:167492780-167492781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549899630	chr6:167492810-167492811	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs549931885	chr6:167492860-167492861	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs369619164	chr6:167492875-167492876	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs568394921	chr6:167492883-167492884	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:3260 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167487000-167494400	Enhancers	Primary B cells from peripheral blood	blood
2	chr6:167487400-167492600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr6:167487600-167492400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr6:167489200-167492200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:167490000-167492600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:167490200-167495600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:167491000-167492800	Enhancers	GM12878-XiMat	blood
8	chr6:167491000-167494400	Enhancers	Primary B cells from cord blood	blood
9	chr6:167491200-167491800	Flanking Active TSS	HepG2	liver
10	chr6:167491400-167491600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:167491400-167492200	Weak transcription	Fetal Muscle Leg	muscle
12	chr6:167491600-167492400	Enhancers	Spleen	Spleen
13	chr6:167491600-167493200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:167491800-167492600	Enhancers	HepG2	liver
15	chr6:167492000-167503400	Weak transcription	Right Atrium	heart
16	chr6:167492200-167492400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr6:167492200-167493000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr6:167492200-167494000	Enhancers	Fetal Muscle Leg	muscle
19	chr6:167492400-167493400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr6:167492400-167493600	Weak transcription	Spleen	Spleen
21	chr6:167492400-167494000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr6:167492600-167493200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:167492600-167494400	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr6:167492800-167493800	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr6:167492800-167494000	Flanking Active TSS	GM12878-XiMat	blood
26	chr6:167493000-167493400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:167493000-167494200	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr6:167493000-167494200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr6:167493200-167493400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr6:167493200-167494000	Enhancers	Primary T cells fromperipheralblood	blood
31	chr6:167493200-167494000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr6:167493200-167494000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr6:167493400-167493600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr6:167493400-167493800	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr6:167493400-167493800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr6:167493400-167494400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr6:167493600-167493800	Enhancers	Spleen	Spleen
38	chr6:167493600-167494000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:167493600-167494200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:167493600-167494200	Enhancers	Fetal Thymus	thymus
41	chr6:167494000-167494200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr6:167494000-167494400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr6:167494000-167494400	Enhancers	GM12878-XiMat	blood
44	chr6:167501800-167502200	ZNF genes & repeats	GM12878-XiMat	blood
45	chr6:167502000-167506000	Enhancers	Primary B cells from peripheral blood	blood
46	chr6:167502200-167503800	Enhancers	GM12878-XiMat	blood
47	chr6:167502200-167504600	Enhancers	Primary B cells from cord blood	blood
48	chr6:167502800-167503200	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr6:167502800-167503400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr6:167502800-167503400	Enhancers	Primary hematopoietic stem cells short term culture	blood

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