Variant report

Variant	nsv428470
Chromosome Location	chr6:11686198-11747850
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1046)
CpG islands
(count:366)
Chromatin interactive
region (count:64)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:11700450-11700677	K562	blood:	n/a	n/a
2	ATF2	chr6:11711447-11713475	GM12878	blood:	n/a	n/a
3	ATF2	chr6:11714151-11715184	GM12878	blood:	n/a	n/a
4	ATF2	chr6:11711528-11713514	GM12878	blood:	n/a	n/a
5	ATF2	chr6:11714214-11715173	GM12878	blood:	n/a	n/a
6	ATF2	chr6:11730505-11731420	GM12878	blood:	n/a	n/a
7	ATF2	chr6:11730661-11731349	GM12878	blood:	n/a	n/a
8	ATF2	chr6:11723045-11723597	GM12878	blood:	n/a	n/a
9	ATF2	chr6:11731801-11733023	GM12878	blood:	n/a	n/a
10	ATF2	chr6:11731922-11733068	GM12878	blood:	n/a	n/a
11	ATF3	chr6:11739061-11739373	K562	blood:	n/a	n/a
12	BATF	chr6:11732110-11732812	GM12878	blood:	n/a	n/a
13	BATF	chr6:11714642-11715052	GM12878	blood:	n/a	n/a
14	BATF	chr6:11730786-11731338	GM12878	blood:	n/a	n/a
15	BATF	chr6:11711882-11712232	GM12878	blood:	n/a	n/a
16	BATF	chr6:11712540-11713419	GM12878	blood:	n/a	n/a
17	BATF	chr6:11732109-11732917	GM12878	blood:	n/a	n/a
18	BATF	chr6:11711547-11712383	GM12878	blood:	n/a	chr6:11711685-11711694
19	BCL11A	chr6:11711922-11712242	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:11732094-11732861	GM12878	blood:	n/a	chr6:11732311-11732320
21	BCL11A	chr6:11730847-11731256	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:11732306-11732763	GM12878	blood:	n/a	chr6:11732311-11732320
23	BCL11A	chr6:11711536-11712395	GM12878	blood:	n/a	n/a
24	BCL3	chr6:11736327-11736806	GM12878	blood:	n/a	n/a
25	BCL3	chr6:11712499-11713504	GM12878	blood:	n/a	n/a
26	BCL3	chr6:11732080-11732799	GM12878	blood:	n/a	chr6:11732311-11732320
27	BCL3	chr6:11711595-11712338	GM12878	blood:	n/a	n/a
28	BCL3	chr6:11730744-11731237	GM12878	blood:	n/a	n/a
29	BCL3	chr6:11732274-11732811	GM12878	blood:	n/a	chr6:11732311-11732320
30	BCL3	chr6:11736345-11736845	GM12878	blood:	n/a	n/a
31	BCL3	chr6:11711932-11712192	GM12878	blood:	n/a	n/a
32	BCL3	chr6:11714513-11715130	GM12878	blood:	n/a	n/a
33	BCLAF1	chr6:11731982-11732930	GM12878	blood:	n/a	chr6:11732311-11732320
34	BCLAF1	chr6:11714163-11715205	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:11714232-11715211	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:11730806-11731469	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:11722434-11723694	GM12878	blood:	n/a	n/a
38	BCLAF1	chr6:11711690-11713903	GM12878	blood:	n/a	n/a
39	BCLAF1	chr6:11730695-11731446	GM12878	blood:	n/a	n/a
40	BCLAF1	chr6:11700351-11700643	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:11711524-11713689	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:11732086-11732876	GM12878	blood:	n/a	chr6:11732311-11732320
43	BHLHE40	chr6:11731691-11731988	HepG2	liver:	n/a	n/a
44	BHLHE40	chr6:11688076-11688116	K562	blood:	n/a	n/a
45	BHLHE40	chr6:11714410-11715020	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:11732155-11733052	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:11711736-11713655	GM12878	blood:	n/a	n/a
48	BHLHE40	chr6:11722467-11722764	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:11730813-11731297	GM12878	blood:	n/a	n/a
50	BRCA1	chr6:11732522-11732831	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:11710597-11710647	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:11714562-11714612	ProgFib	skin:	n/a
3	chr6:11710597-11710647	NHDF-neo	bronchial:	n/a
4	chr6:11711971-11712021	GM19239	blood:	n/a
5	chr6:11686518-11686568	BJ	skin:	n/a
6	chr6:11711971-11712021	IMR90	lung:	fetal
7	chr6:11687689-11687739	HRPEpiC	eye:	n/a
8	chr6:11702389-11702439	PFSK-1	brain:	n/a
9	chr6:11702389-11702439	NT2-D1	testis:	n/a
10	chr6:11714562-11714612	HepG2	liver:	n/a
11	chr6:11686518-11686568	NHDF-neo	bronchial:	n/a
12	chr6:11702389-11702439	RPTEC	kidney:	n/a
13	chr6:11710597-11710647	NH-A	brain:	n/a
14	chr6:11710597-11710647	A549	lung:	n/a
15	chr6:11710597-11710647	BE2_C	brain:	n/a
16	chr6:11687689-11687739	HIPEpiC	eye:	n/a
17	chr6:11714562-11714612	A549	lung:	n/a
18	chr6:11711971-11712021	PrEC	prostate:	n/a
19	chr6:11710597-11710647	MCF10A-Er-Src	breast:	n/a
20	chr6:11686518-11686568	BE2_C	brain:	n/a
21	chr6:11710597-11710647	SK-N-SH_RA	brain:	n/a
22	chr6:11710597-11710647	NHBE	bronchial:	n/a
23	chr6:11711971-11712021	Jurkat	blood:	n/a
24	chr6:11687689-11687739	K562	blood:	n/a
25	chr6:11710597-11710647	RPTEC	kidney:	n/a
26	chr6:11711971-11712021	HIPEpiC	eye:	n/a
27	chr6:11710597-11710647	GM12878	blood:	n/a
28	chr6:11687689-11687739	Caco-2	colon:	n/a
29	chr6:11710597-11710647	HNPCEpiC	eye:	n/a
30	chr6:11711971-11712021	ovcar-3	ovarian:	n/a
31	chr6:11710597-11710647	AoSMC	blood vessel:	n/a
32	chr6:11711971-11712021	HMEC	breast:	n/a
33	chr6:11710597-11710647	PrEC	prostate:	n/a
34	chr6:11714562-11714612	U87	brain:	n/a
35	chr6:11687689-11687739	GM19239	blood:	n/a
36	chr6:11702389-11702439	LNCaP	prostate:	n/a
37	chr6:11702389-11702439	SK-N-MC	brain:	n/a
38	chr6:11714562-11714612	HEK293	kidney:	embryo
39	chr6:11710597-11710647	Hela-S3	cervix:	n/a
40	chr6:11702389-11702439	U87	brain:	n/a
41	chr6:11714562-11714612	IMR90	lung:	fetal
42	chr6:11686518-11686568	HCF	heart:	n/a
43	chr6:11686518-11686568	SAEC	small airway:	n/a
44	chr6:11714562-11714612	HNPCEpiC	eye:	n/a
45	chr6:11714562-11714612	BJ	skin:	n/a
46	chr6:11687689-11687739	GM12891	blood:	n/a
47	chr6:11702389-11702439	NH-A	brain:	n/a
48	chr6:11714562-11714612	NT2-D1	testis:	n/a
49	chr6:11711971-11712021	A549	lung:	n/a
50	chr6:11711971-11712021	Hela-S3	cervix:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:11685508..11687716-chr6:11690185..11693002,2	MCF-7	breast:
2	chr6:11707605..11709932-chr6:11714222..11716200,2	K562	blood:
3	chr15:52972928..52973805-chr6:11737938..11738770,2	MCF-7	breast:
4	chr6:11695198..11695698-chr6:12075562..12076076,2	MCF-7	breast:
5	chr6:11723063..11725185-chr6:11732645..11735491,2	K562	blood:
6	chr6:11745914..11747958-chr6:11748915..11751495,2	MCF-7	breast:
7	chr6:11695236..11697573-chr6:11698508..11700443,2	MCF-7	breast:
8	chr6:11743986..11745912-chr6:11747510..11751154,3	MCF-7	breast:
9	chr6:11717348..11719875-chr6:11747463..11750048,2	MCF-7	breast:
10	chr6:11701505..11703712-chr6:12008102..12010542,2	MCF-7	breast:
11	chr6:11717459..11719677-chr6:11722650..11725386,2	MCF-7	breast:
12	chr6:11715212..11717961-chr6:11734201..11736485,2	K562	blood:
13	chr6:11728883..11730943-chr6:11731032..11732727,2	K562	blood:
14	chr6:11696852..11698395-chr6:11698411..11700271,2	K562	blood:
15	chr6:11691117..11693663-chr6:11695839..11698577,2	K562	blood:
16	chr6:11701557..11703437-chr6:11705057..11706744,2	K562	blood:
17	chr6:11716333..11720276-chr6:11720959..11723559,3	K562	blood:
18	chr6:11717459..11719677-chr6:11722650..11725386,2	MCF-7	breast:
19	chr6:11704392..11707213-chr6:11707810..11709507,2	K562	blood:
20	chr6:11675436..11677701-chr6:11686415..11688887,2	MCF-7	breast:
21	chr6:11707605..11709932-chr6:11714222..11716200,2	K562	blood:
22	chr6:11685508..11687716-chr6:11690185..11693002,2	MCF-7	breast:
23	chr6:11700330..11700838-chr6:11912516..11913089,2	MCF-7	breast:
24	chr6:11710777..11713015-chr6:11730009..11731518,2	K562	blood:
25	chr6:11700027..11700890-chr6:12034347..12035299,2	MCF-7	breast:
26	chr6:11722035..11725191-chr6:11730801..11735491,4	K562	blood:
27	chr6:11733150..11736062-chr6:12007778..12010289,2	K562	blood:
28	chr6:11743683..11746205-chr6:11753336..11755527,2	K562	blood:
29	chr6:11685812..11688101-chr6:11689840..11692824,2	K562	blood:
30	chr6:11742447..11744431-chr6:11745938..11748190,2	K562	blood:
31	chr6:11737947..11739936-chr6:11767756..11769331,2	MCF-7	breast:
32	chr6:11734066..11736149-chr6:11741564..11743376,2	MCF-7	breast:
33	chr6:11701557..11703437-chr6:11705057..11706744,2	K562	blood:
34	chr6:11718348..11720271-chr6:11754971..11757663,2	K562	blood:
35	chr6:11695236..11697573-chr6:11698508..11700443,2	MCF-7	breast:
36	chr6:11743986..11745912-chr6:11747510..11751154,3	MCF-7	breast:
37	chr6:11700039..11702996-chr6:11707922..11710740,2	K562	blood:
38	chr6:11731733..11734169-chr6:11735074..11737583,2	K562	blood:
39	chr6:11726535..11729461-chr6:11731362..11733356,2	MCF-7	breast:
40	chr6:11722035..11725191-chr6:11730801..11735491,4	K562	blood:
41	chr6:11700114..11701011-chr6:12289302..12289986,2	K562	blood:
42	chr6:11696852..11698395-chr6:11698411..11700271,2	K562	blood:
43	chr6:11710372..11713269-chr6:11723329..11725416,2	K562	blood:
44	chr6:11728883..11730943-chr6:11731032..11732727,2	K562	blood:
45	chr6:11717348..11719875-chr6:11747463..11750048,2	MCF-7	breast:
46	chr6:11690358..11691945-chr6:12011366..12013423,2	MCF-7	breast:
47	chr6:11740535..11742898-chr6:11758594..11760126,2	K562	blood:
48	chr6:11723063..11725185-chr6:11732645..11735491,2	K562	blood:
49	chr6:11704392..11707213-chr6:11707810..11709507,2	K562	blood:
50	chr6:11733831..11736245-chr6:11739870..11742383,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEDD9-2	chr6:11723582-11723733	NONHSAT107762
2	lnc-NEDD9-2	chr6:11735801-11735916	NONHSAT107762
3	lnc-NEDD9-2	chr6:11736237-11736947	NONHSAT107762
4	lnc-NEDD9-2	chr6:11713908-11714745	NONHSAT107762
5	lnc-NEDD9-2	chr6:11723582-11723733	NONHSAT107763
6	lnc-NEDD9-2	chr6:11714187-11714745	NONHSAT107763
7	lnc-NEDD9-2	chr6:11728560-11728790	NONHSAT107763
8	lnc-NEDD9-2	chr6:11717542-11717647	NONHSAT107762

No data

Variant related genes	Relation type
ADTRP	TF binding region
ENSG00000207419	TF binding region
ADTRP	CpG island
ENSG00000207419	CpG island
ENSG00000095951	chromatin interactions
ENSG00000111863	chromatin interactions
ENSG00000229896	chromatin interactions
ENSG00000207419	chromatin interactions

Extended variants
information (count: 2399 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2399 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146327968	chr6:11686202-11686203	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs10947516	chr6:11686227-11686228	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs139179534	chr6:11686244-11686245	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs528479596	chr6:11686261-11686262	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs76542477	chr6:11686262-11686263	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs114757334	chr6:11686265-11686266	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs537572217	chr6:11686337-11686338	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs372302814	chr6:11686358-11686359	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs557477219	chr6:11686375-11686376	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs190355865	chr6:11686400-11686401	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs12173585	chr6:11686438-11686439	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs553396205	chr6:11686440-11686441	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs183522778	chr6:11686473-11686474	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs573446542	chr6:11686498-11686499	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs150883116	chr6:11686518-11686519	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs376860832	chr6:11686523-11686524	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs139333268	chr6:11686524-11686525	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs149642361	chr6:11686527-11686528	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs12175829	chr6:11686533-11686534	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs144411659	chr6:11686538-11686539	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs74393752	chr6:11686544-11686545	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs536988369	chr6:11686545-11686546	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs556833765	chr6:11686549-11686550	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs376251218	chr6:11686560-11686561	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs12175836	chr6:11686566-11686567	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs140179167	chr6:11686575-11686576	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs79703904	chr6:11686597-11686598	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530894236	chr6:11686599-11686600	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs6924450	chr6:11686613-11686614	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs570914162	chr6:11686642-11686643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146660464	chr6:11686659-11686660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553568415	chr6:11686680-11686681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113492104	chr6:11686720-11686721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142538702	chr6:11686745-11686746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10947517	chr6:11686782-11686783	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533144612	chr6:11686792-11686793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150986446	chr6:11686809-11686810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10947518	chr6:11686844-11686845	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs75025262	chr6:11686845-11686846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576832038	chr6:11686870-11686871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188803358	chr6:11686881-11686882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140851931	chr6:11686894-11686895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370033216	chr6:11686918-11686919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76378998	chr6:11686926-11686927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535002037	chr6:11686927-11686928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201505530	chr6:11686936-11686937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199782925	chr6:11686937-11686938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35136486	chr6:11686950-11686951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572938166	chr6:11686965-11686966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542125273	chr6:11686990-11686991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Cancer	21183584	CNVD
Acute myeloid leukemia	18000384	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Metastatic melanoma	18483359	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1092 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11681600-11687600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:11684200-11688200	Enhancers	Fetal Intestine Small	intestine
3	chr6:11684800-11688600	Enhancers	Placenta Amnion	Placenta Amnion
4	chr6:11685000-11686600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr6:11685000-11686600	Flanking Active TSS	A549	lung
6	chr6:11685000-11686600	Enhancers	HSMM	muscle
7	chr6:11685000-11686600	Enhancers	HSMMtube	muscle
8	chr6:11685000-11686800	Enhancers	Hela-S3	cervix
9	chr6:11685000-11687000	Enhancers	Placenta	Placenta
10	chr6:11685000-11688600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:11685000-11689400	Enhancers	Fetal Intestine Large	intestine
12	chr6:11685200-11686600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr6:11685200-11686600	Enhancers	NH-A	brain
14	chr6:11685200-11686600	Enhancers	Osteobl	bone
15	chr6:11685200-11686800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:11685200-11688400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:11685200-11693000	Weak transcription	Spleen	Spleen
18	chr6:11685400-11688800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr6:11685600-11686400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:11685600-11686800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:11685800-11686200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr6:11685800-11686200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:11685800-11686200	Flanking Active TSS	HMEC	breast
24	chr6:11685800-11686200	Flanking Active TSS	NHEK	skin
25	chr6:11685800-11686600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr6:11685800-11687000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:11685800-11687600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:11686000-11686400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr6:11686000-11686600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:11686000-11686600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr6:11686000-11686600	Enhancers	NHLF	lung
32	chr6:11686000-11687200	Weak transcription	Fetal Heart	heart
33	chr6:11686200-11686400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:11686200-11686600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr6:11686200-11686600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:11686200-11686600	Enhancers	Ovary	ovary
37	chr6:11686200-11686600	Enhancers	NHDF-Ad	bronchial
38	chr6:11686200-11687000	Enhancers	NHEK	skin
39	chr6:11686200-11687200	Enhancers	HMEC	breast
40	chr6:11686200-11687400	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr6:11686400-11686600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr6:11686400-11687400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:11686600-11687000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr6:11686600-11687000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:11686600-11687000	Enhancers	A549	lung
46	chr6:11686600-11687200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr6:11686600-11687400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr6:11686600-11687600	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr6:11686600-11687800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr6:11686600-11687800	Weak transcription	Ovary	ovary

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