Variant report

Variant	nsv1022881
Chromosome Location	chr6:140098646-140172570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:460)
CpG islands
(count:184)
Chromatin interactive
region (count:56)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:140144369-140145073	K562	blood:	n/a	n/a
2	ARID3A	chr6:140098435-140098677	K562	blood:	n/a	n/a
3	ARID3A	chr6:140150275-140150946	K562	blood:	n/a	n/a
4	ARID3A	chr6:140146632-140147540	K562	blood:	n/a	n/a
5	ATF1	chr6:140144695-140145052	K562	blood:	n/a	n/a
6	ATF1	chr6:140147094-140147505	K562	blood:	n/a	n/a
7	ATF3	chr6:140144598-140145075	K562	blood:	n/a	n/a
8	BACH1	chr6:140147036-140147514	K562	blood:	n/a	n/a
9	BACH1	chr6:140123194-140123429	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr6:140162926-140163284	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:140162961-140163282	GM12878	blood:	n/a	chr6:140163170-140163179 chr6:140162999-140163008 chr6:140163152-140163161
12	BCL11A	chr6:140162949-140163299	GM12878	blood:	n/a	chr6:140163170-140163179 chr6:140162999-140163008 chr6:140163152-140163161
13	BHLHE40	chr6:140147170-140147626	K562	blood:	n/a	n/a
14	BHLHE40	chr6:140162903-140163364	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:140098409-140098805	K562	blood:	n/a	n/a
16	BHLHE40	chr6:140144238-140145040	K562	blood:	n/a	n/a
17	CBX3	chr6:140125787-140126257	K562	blood:	n/a	n/a
18	CBX3	chr6:140098356-140098790	K562	blood:	n/a	n/a
19	CBX3	chr6:140105340-140105870	K562	blood:	n/a	n/a
20	CBX3	chr6:140146793-140147633	K562	blood:	n/a	n/a
21	CBX3	chr6:140105288-140105897	K562	blood:	n/a	n/a
22	CBX3	chr6:140147051-140147581	K562	blood:	n/a	n/a
23	CCNT2	chr6:140151128-140151279	K562	blood:	n/a	n/a
24	CCNT2	chr6:140144775-140145197	K562	blood:	n/a	n/a
25	CCNT2	chr6:140146733-140147402	K562	blood:	n/a	n/a
26	CCNT2	chr6:140098366-140098717	K562	blood:	n/a	chr6:140098586-140098595
27	CEBPB	chr6:140144558-140145237	K562	blood:	n/a	chr6:140145045-140145056 chr6:140145047-140145058
28	CEBPB	chr6:140156050-140156250	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:140104353-140104355	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr6:140156070-140156270	K562	blood:	n/a	n/a
31	CEBPB	chr6:140156055-140156252	K562	blood:	n/a	n/a
32	CEBPB	chr6:140146841-140147580	K562	blood:	n/a	n/a
33	CEBPB	chr6:140144538-140145233	K562	blood:	n/a	chr6:140145045-140145056 chr6:140145047-140145058
34	CEBPB	chr6:140137168-140137368	K562	blood:	n/a	chr6:140137231-140137242
35	CEBPB	chr6:140098404-140098688	K562	blood:	n/a	chr6:140098407-140098424
36	CEBPB	chr6:140137163-140137280	HepG2	liver:	n/a	chr6:140137231-140137242
37	CEBPB	chr6:140144770-140145190	HepG2	liver:	n/a	chr6:140145045-140145056 chr6:140145047-140145058
38	CEBPB	chr6:140098256-140098759	K562	blood:	n/a	chr6:140098407-140098424
39	CEBPB	chr6:140168607-140168778	H1-hESC	embryonic stem cell:	n/a	chr6:140168723-140168736
40	CEBPB	chr6:140098357-140098729	K562	blood:	n/a	chr6:140098407-140098424
41	CEBPB	chr6:140124006-140124598	HepG2	liver:	n/a	chr6:140124156-140124167 chr6:140124156-140124169 chr6:140124157-140124168
42	CEBPB	chr6:140146958-140147505	K562	blood:	n/a	n/a
43	CEBPD	chr6:140144649-140145144	K562	blood:	n/a	n/a
44	CEBPD	chr6:140144576-140145256	K562	blood:	n/a	n/a
45	CEBPD	chr6:140146793-140147529	K562	blood:	n/a	n/a
46	CEBPD	chr6:140161671-140162257	K562	blood:	n/a	n/a
47	CHD1	chr6:140163396-140163471	GM12878	blood:	n/a	n/a
48	CHD2	chr6:140162946-140163353	GM12878	blood:	n/a	n/a
49	CHD2	chr6:140161054-140161123	GM12878	blood:	n/a	n/a
50	CHD2	chr6:140098414-140098818	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:140141165-140141215	HNPCEpiC	eye:	n/a
2	chr6:140141165-140141215	HNPCEpiC	eye:	n/a
3	chr6:140098850-140098900	NHBE	bronchial:	n/a
4	chr6:140141165-140141215	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:140141165-140141215	AG09309	skin:	n/a
6	chr6:140141165-140141215	U87	brain:	n/a
7	chr6:140141165-140141215	LNCaP	prostate:	n/a
8	chr6:140098850-140098900	AG09319	gingival:	n/a
9	chr6:140098850-140098900	LNCaP	prostate:	n/a
10	chr6:140141165-140141215	ProgFib	skin:	n/a
11	chr6:140141165-140141215	Caco-2	colon:	n/a
12	chr6:140098850-140098900	NHDF-neo	bronchial:	n/a
13	chr6:140141165-140141215	GM12891	blood:	n/a
14	chr6:140098850-140098900	ovcar-3	ovarian:	n/a
15	chr6:140098850-140098900	HCM	heart:	n/a
16	chr6:140098850-140098900	NT2-D1	testis:	n/a
17	chr6:140098850-140098900	AoSMC	blood vessel:	n/a
18	chr6:140168822-140168872	T-47D	breast:	n/a
19	chr6:140168822-140168872	GM19239	blood:	n/a
20	chr6:140098850-140098900	K562	blood:	n/a
21	chr6:140168822-140168872	AG09309	skin:	n/a
22	chr6:140098850-140098900	NB4	blood:	n/a
23	chr6:140141165-140141215	A549	lung:	n/a
24	chr6:140168822-140168872	HL-60	blood:	n/a
25	chr6:140168822-140168872	HRPEpiC	eye:	n/a
26	chr6:140098850-140098900	MCF10A-Er-Src	breast:	n/a
27	chr6:140168822-140168872	U87	brain:	n/a
28	chr6:140141165-140141215	SK-N-SH_RA	brain:	n/a
29	chr6:140098850-140098900	HNPCEpiC	eye:	n/a
30	chr6:140141165-140141215	HL-60	blood:	n/a
31	chr6:140168822-140168872	LNCaP	prostate:	n/a
32	chr6:140098850-140098900	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:140168822-140168872	CMK	blood:	n/a
34	chr6:140098850-140098900	RPTEC	kidney:	n/a
35	chr6:140141165-140141215	HCM	heart:	n/a
36	chr6:140141165-140141215	ECC-1	luminal epithelium:	n/a
37	chr6:140141165-140141215	H1-hESC	embryonic stem cell:	embryo
38	chr6:140168822-140168872	Caco-2	colon:	n/a
39	chr6:140168822-140168872	SK-N-SH_RA	brain:	n/a
40	chr6:140168822-140168872	HCM	heart:	n/a
41	chr6:140141165-140141215	NHDF-neo	bronchial:	n/a
42	chr6:140141165-140141215	HepG2	liver:	n/a
43	chr6:140141165-140141215	IMR90	lung:	fetal
44	chr6:140141165-140141215	HRE	kidney:	n/a
45	chr6:140098850-140098900	MCF-7	breast:	n/a
46	chr6:140098850-140098900	NH-A	brain:	n/a
47	chr6:140141165-140141215	SK-N-SH	brain:	n/a
48	chr6:140098850-140098900	ProgFib	skin:	n/a
49	chr6:140098850-140098900	HepG2	liver:	n/a
50	chr6:140141165-140141215	GM12892	blood:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:140147200..140149310-chr6:140258433..140260854,2	K562	blood:
2	chr6:140144961..140147282-chr6:140158206..140160311,2	K562	blood:
3	chr6:140123522..140126295-chr6:140134268..140137009,2	K562	blood:
4	chr6:140151820..140155289-chr6:140156811..140159238,3	K562	blood:
5	chr6:140091742..140094487-chr6:140097779..140099981,2	K562	blood:
6	chr6:139694049..139695787-chr6:140096448..140099243,2	K562	blood:
7	chr6:140143575..140149328-chr6:140151123..140155301,5	MCF-7	breast:
8	chr6:140109282..140111631-chr6:140114175..140116181,2	K562	blood:
9	chr6:139695107..139696860-chr6:140141240..140143122,2	K562	blood:
10	chr6:140147996..140150360-chr6:140164145..140166943,2	MCF-7	breast:
11	chr6:139693600..139695458-chr6:140131244..140133908,2	K562	blood:
12	chr6:140133269..140136209-chr6:140137341..140139354,2	MCF-7	breast:
13	chr6:140096649..140099517-chr6:140260643..140262599,2	K562	blood:
14	chr6:140143350..140145864-chr6:140147997..140150227,3	K562	blood:
15	chr6:140143575..140149328-chr6:140151123..140155301,5	MCF-7	breast:
16	chr6:140169517..140172287-chr6:140175933..140178013,2	MCF-7	breast:
17	chr6:139930810..139933752-chr6:140097356..140098943,2	K562	blood:
18	chr6:140086666..140088704-chr6:140112529..140114998,2	K562	blood:
19	chr6:140140102..140141609-chr6:140143434..140145360,2	K562	blood:
20	chr6:140145227..140147180-chr6:140155526..140157728,3	K562	blood:
21	chr6:139694026..139696985-chr6:140124355..140126550,2	K562	blood:
22	chr6:139693562..139695067-chr6:140162758..140164273,2	K562	blood:
23	chr6:140137505..140139416-chr6:140141678..140144542,3	K562	blood:
24	chr6:140143350..140145864-chr6:140147997..140150227,3	K562	blood:
25	chr6:140148977..140151399-chr6:140177571..140180376,2	K562	blood:
26	chr6:140128805..140131673-chr6:141152750..141154839,2	K562	blood:
27	chr6:139694861..139698914-chr6:140150026..140153198,5	K562	blood:
28	chr6:139694383..139697089-chr6:140144858..140146538,2	MCF-7	breast:
29	chr6:140148096..140149625-chr6:140150538..140152679,2	K562	blood:
30	chr6:140140156..140142876-chr6:140150125..140152606,2	K562	blood:
31	chr6:140123522..140126295-chr6:140134268..140137009,2	K562	blood:
32	chr6:140137505..140139416-chr6:140141678..140144542,3	K562	blood:
33	chr6:140091742..140094049-chr6:140096525..140099279,2	K562	blood:
34	chr20:56744882..56745609-chr6:140167540..140168267,2	MCF-7	breast:
35	chr6:140101468..140104254-chr6:140123458..140124998,2	K562	blood:
36	chr6:139773415..139775962-chr6:140133812..140135963,2	K562	blood:
37	chr6:140140156..140142876-chr6:140150125..140152606,2	K562	blood:
38	chr6:140143855..140145864-chr6:140148149..140150227,2	K562	blood:
39	chr6:139693685..139697064-chr6:140156234..140158195,3	K562	blood:
40	chr6:140145227..140147180-chr6:140155526..140157728,3	K562	blood:
41	chr6:140143855..140145864-chr6:140148149..140150227,2	K562	blood:
42	chr6:139695846..139697718-chr6:140097081..140099970,2	K562	blood:
43	chr6:140098817..140100684-chr6:140317042..140318702,2	MCF-7	breast:
44	chr6:140171085..140173859-chr6:140174869..140177839,3	K562	blood:
45	chr6:140147996..140150360-chr6:140164145..140166943,2	MCF-7	breast:
46	chr6:140144961..140147282-chr6:140158206..140160311,2	K562	blood:
47	chr6:140163093..140164659-chr6:140165624..140167257,2	MCF-7	breast:
48	chr6:139694314..139696643-chr6:140160154..140162718,2	K562	blood:
49	chr6:140163093..140164659-chr6:140165624..140167257,2	MCF-7	breast:
50	chr6:139694287..139696985-chr6:140124308..140125855,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000231426	TF binding region
ENSG00000231426	CpG island
ENSG00000164442	chromatin interactions
ENSG00000231426	chromatin interactions

Extended variants
information (count: 1943 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1943 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9376464	chr6:140098717-140098718	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547006434	chr6:140098729-140098730	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529034138	chr6:140098734-140098735	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370008088	chr6:140098753-140098754	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535710965	chr6:140098759-140098760	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs148533053	chr6:140098841-140098842	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576061340	chr6:140098890-140098891	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377704966	chr6:140098893-140098894	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs79545391	chr6:140098954-140098955	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142846088	chr6:140099121-140099122	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs151038338	chr6:140099158-140099159	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549294903	chr6:140099159-140099160	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574532510	chr6:140099198-140099199	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541659482	chr6:140099214-140099215	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs142322858	chr6:140099239-140099240	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569048704	chr6:140099243-140099244	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs116350007	chr6:140099265-140099266	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs546352129	chr6:140099278-140099279	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs564450887	chr6:140099308-140099309	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs181249648	chr6:140099390-140099391	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs186342097	chr6:140099391-140099392	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs62430237	chr6:140099416-140099417	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs547262184	chr6:140099503-140099504	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs147950424	chr6:140099556-140099557	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs111571400	chr6:140099565-140099566	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs550916355	chr6:140099590-140099591	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs558445876	chr6:140099714-140099715	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs536735806	chr6:140099728-140099729	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs202153583	chr6:140099802-140099803	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570113357	chr6:140099805-140099806	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs7751292	chr6:140099836-140099837	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs553602443	chr6:140099842-140099843	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs553183810	chr6:140099886-140099887	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs374352281	chr6:140099889-140099890	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs574663564	chr6:140099902-140099903	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs541972109	chr6:140099965-140099966	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs556861653	chr6:140099991-140099992	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs370426739	chr6:140100042-140100043	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs370695007	chr6:140100044-140100045	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs575536711	chr6:140100061-140100062	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs141790671	chr6:140100089-140100090	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs150453951	chr6:140100101-140100102	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs528454719	chr6:140100116-140100117	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs540271514	chr6:140100119-140100120	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs562379134	chr6:140100151-140100152	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs551488569	chr6:140100152-140100153	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs78240637	chr6:140100164-140100165	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs138007663	chr6:140100192-140100193	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs533397099	chr6:140100212-140100213	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs571628934	chr6:140100246-140100247	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	21448237	CNVD
Autism	22495311	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
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140086000-140099400	Weak transcription	Ovary	ovary
2	chr6:140086000-140101000	Weak transcription	Left Ventricle	heart
3	chr6:140087400-140099200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr6:140088200-140100000	Weak transcription	NHDF-Ad	bronchial
5	chr6:140096200-140100800	Enhancers	K562	blood
6	chr6:140096400-140099000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:140096400-140100200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr6:140096400-140100200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:140096400-140100400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:140096400-140100400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:140096400-140100800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:140096600-140100400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:140096800-140099000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:140096800-140099000	Enhancers	Stomach Smooth Muscle	stomach
15	chr6:140096800-140099600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr6:140097000-140099600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr6:140097000-140099600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr6:140097000-140100000	Enhancers	Fetal Heart	heart
19	chr6:140097000-140100200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr6:140097000-140100600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr6:140097000-140101000	Enhancers	Rectal Smooth Muscle	rectum
22	chr6:140097200-140099200	Enhancers	Brain Germinal Matrix	brain
23	chr6:140097200-140099200	Enhancers	Colon Smooth Muscle	Colon
24	chr6:140097200-140099600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:140097200-140100200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:140097200-140100400	Enhancers	Fetal Brain Male	brain
27	chr6:140097400-140099400	Weak transcription	NHLF	lung
28	chr6:140097400-140099600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr6:140097400-140100600	Enhancers	Fetal Stomach	stomach
30	chr6:140097600-140099000	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr6:140098000-140098800	Weak transcription	Fetal Kidney	kidney
32	chr6:140098000-140099000	Weak transcription	Fetal Muscle Leg	muscle
33	chr6:140098000-140099400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:140098000-140099400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr6:140098000-140099400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr6:140098000-140100800	Enhancers	Fetal Brain Female	brain
37	chr6:140098200-140100200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:140098400-140099000	Enhancers	Stomach Mucosa	stomach
39	chr6:140098400-140099600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:140098600-140099400	Weak transcription	Pancreas	Pancrea
41	chr6:140098600-140099600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:140098600-140100000	Weak transcription	Fetal Lung	lung
43	chr6:140098600-140100200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:140098600-140100400	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr6:140098800-140099600	Enhancers	Fetal Kidney	kidney
46	chr6:140099000-140099200	Flanking Active TSS	Stomach Smooth Muscle	stomach
47	chr6:140099000-140099600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:140099000-140100000	Weak transcription	Stomach Mucosa	stomach
49	chr6:140099000-140100200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:140099000-140100200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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