Variant report

Variant	esv2763359
Chromosome Location	chr4:48189710-48290233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2400)
CpG islands
(count:1281)
Chromatin interactive
region (count:114)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2400 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48271156-48271462	K562	blood:	n/a	n/a
2	ARID3A	chr4:48189758-48190105	K562	blood:	n/a	n/a
3	ARID3A	chr4:48245400-48245848	K562	blood:	n/a	n/a
4	ARID3A	chr4:48231013-48231317	K562	blood:	n/a	n/a
5	ARID3A	chr4:48249420-48249934	K562	blood:	n/a	n/a
6	ARID3A	chr4:48271978-48272494	K562	blood:	n/a	n/a
7	ARID3A	chr4:48236621-48236842	K562	blood:	n/a	n/a
8	ARID3A	chr4:48277272-48277623	K562	blood:	n/a	n/a
9	ARID3A	chr4:48214291-48214523	K562	blood:	n/a	n/a
10	ARID3A	chr4:48205747-48206212	K562	blood:	n/a	n/a
11	ARID3A	chr4:48199618-48200001	K562	blood:	n/a	n/a
12	ARID3A	chr4:48260893-48260896	K562	blood:	n/a	n/a
13	ATF1	chr4:48272999-48273508	K562	blood:	n/a	n/a
14	ATF1	chr4:48257322-48257741	K562	blood:	n/a	n/a
15	ATF1	chr4:48231005-48231283	K562	blood:	n/a	n/a
16	ATF1	chr4:48254522-48254801	K562	blood:	n/a	n/a
17	ATF1	chr4:48249224-48249377	K562	blood:	n/a	n/a
18	ATF1	chr4:48214196-48214612	K562	blood:	n/a	n/a
19	ATF1	chr4:48189913-48190232	K562	blood:	n/a	n/a
20	ATF1	chr4:48240069-48240358	K562	blood:	n/a	n/a
21	ATF1	chr4:48245408-48245828	K562	blood:	n/a	n/a
22	ATF1	chr4:48205774-48206215	K562	blood:	n/a	n/a
23	ATF1	chr4:48221517-48221791	K562	blood:	n/a	n/a
24	ATF2	chr4:48214100-48214829	GM12878	blood:	n/a	n/a
25	ATF2	chr4:48271888-48272435	GM12878	blood:	n/a	n/a
26	ATF2	chr4:48271260-48271747	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr4:48271289-48271867	GM12878	blood:	n/a	n/a
28	ATF2	chr4:48213476-48214744	GM12878	blood:	n/a	n/a
29	ATF2	chr4:48205274-48206233	GM12878	blood:	n/a	n/a
30	ATF2	chr4:48197230-48199822	GM12878	blood:	n/a	n/a
31	ATF2	chr4:48272043-48272668	GM12878	blood:	n/a	n/a
32	ATF2	chr4:48205320-48205690	GM12878	blood:	n/a	n/a
33	ATF2	chr4:48212319-48212836	GM12878	blood:	n/a	n/a
34	ATF2	chr4:48198537-48199201	GM12878	blood:	n/a	n/a
35	ATF2	chr4:48249067-48249653	GM12878	blood:	n/a	n/a
36	ATF3	chr4:48205350-48205758	GM12878	blood:	n/a	n/a
37	ATF3	chr4:48245345-48245736	K562	blood:	n/a	n/a
38	ATF3	chr4:48205452-48205645	GM12878	blood:	n/a	n/a
39	ATF3	chr4:48257249-48257555	K562	blood:	n/a	n/a
40	BACH1	chr4:48249168-48249564	K562	blood:	n/a	n/a
41	BACH1	chr4:48271474-48271674	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr4:48253636-48253639	K562	blood:	n/a	n/a
43	BACH1	chr4:48221513-48221723	K562	blood:	n/a	n/a
44	BACH1	chr4:48243964-48243982	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr4:48272139-48272826	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr4:48271610-48271743	K562	blood:	n/a	n/a
47	BACH1	chr4:48277512-48277519	K562	blood:	n/a	n/a
48	BACH1	chr4:48272285-48272805	K562	blood:	n/a	n/a
49	BATF	chr4:48249174-48249528	GM12878	blood:	n/a	chr4:48249376-48249387
50	BATF	chr4:48199524-48199861	GM12878	blood:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48273240-48273290	NB4	blood:	n/a
2	chr4:48231543-48231593	Hepatocyte	liver:	n/a
3	chr4:48269743-48269793	HepG2	liver:	n/a
4	chr4:48272513-48272563	Jurkat	blood:	n/a
5	chr4:48271835-48271885	NT2-D1	testis:	n/a
6	chr4:48257144-48257194	HRE	kidney:	n/a
7	chr4:48271107-48271157	NHBE	bronchial:	n/a
8	chr4:48272059-48272109	GM12892	blood:	n/a
9	chr4:48269743-48269793	U87	brain:	n/a
10	chr4:48271826-48271876	PFSK-1	brain:	n/a
11	chr4:48272266-48272316	HIPEpiC	eye:	n/a
12	chr4:48271942-48271992	PANC-1	pancreas:	n/a
13	chr4:48272059-48272109	IMR90	lung:	fetal
14	chr4:48269743-48269793	HEK293	kidney:	embryo
15	chr4:48271149-48271199	LNCaP	prostate:	n/a
16	chr4:48271835-48271885	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:48272297-48272347	NHDF-neo	bronchial:	n/a
18	chr4:48271923-48271973	AoSMC	blood vessel:	n/a
19	chr4:48271835-48271885	PrEC	prostate:	n/a
20	chr4:48271107-48271157	MCF-7	breast:	n/a
21	chr4:48271149-48271199	HEK293	kidney:	embryo
22	chr4:48271072-48271122	GM19239	blood:	n/a
23	chr4:48272120-48272170	ProgFib	skin:	n/a
24	chr4:48272513-48272563	IMR90	lung:	fetal
25	chr4:48231543-48231593	HMEC	breast:	n/a
26	chr4:48272513-48272563	HNPCEpiC	eye:	n/a
27	chr4:48269743-48269793	HRE	kidney:	n/a
28	chr4:48231543-48231593	SKMC	muscle:	n/a
29	chr4:48272120-48272170	NB4	blood:	n/a
30	chr4:48257144-48257194	NB4	blood:	n/a
31	chr4:48272059-48272109	BE2_C	brain:	n/a
32	chr4:48271923-48271973	SAEC	small airway:	n/a
33	chr4:48272513-48272563	A549	lung:	n/a
34	chr4:48271826-48271876	GM12878	blood:	n/a
35	chr4:48272120-48272170	AG10803	skin:	n/a
36	chr4:48272297-48272347	BE2_C	brain:	n/a
37	chr4:48271918-48271968	ovcar-3	ovarian:	n/a
38	chr4:48271923-48271973	HAEpiC	amniotic membrane:	n/a
39	chr4:48271893-48271943	T-47D	breast:	n/a
40	chr4:48257144-48257194	PANC-1	pancreas:	n/a
41	chr4:48272297-48272347	Hela-S3	cervix:	n/a
42	chr4:48271835-48271885	Hela-S3	cervix:	n/a
43	chr4:48271826-48271876	AG09309	skin:	n/a
44	chr4:48272297-48272347	HRE	kidney:	n/a
45	chr4:48231543-48231593	AG09309	skin:	n/a
46	chr4:48231543-48231593	SK-N-SH_RA	brain:	n/a
47	chr4:48272120-48272170	Jurkat	blood:	n/a
48	chr4:48271121-48271171	NHBE	bronchial:	n/a
49	chr4:48271149-48271199	AG09309	skin:	n/a
50	chr4:48272077-48272127	HCPEpiC	choroid plexus:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:48251770..48253352-chr4:48260141..48262130,2	K562	blood:
2	chr4:48256167..48259627-chr4:48260322..48264297,6	K562	blood:
3	chr4:48214281..48216760-chr4:48261228..48263562,2	K562	blood:
4	chr4:48255487..48257034-chr4:48270351..48271892,2	K562	blood:
5	chr4:48264879..48267835-chr4:48269527..48271829,4	K562	blood:
6	chr4:48238807..48240507-chr4:48244867..48247720,2	K562	blood:
7	chr17:42297784..42298646-chr4:48271426..48272068,2	Hela-S3	cervix:
8	chr4:48256167..48259627-chr4:48260322..48264297,6	K562	blood:
9	chr4:48191196..48193426-chr4:48194546..48197180,3	K562	blood:
10	chr4:48211265..48214247-chr4:48216270..48217913,2	K562	blood:
11	chr4:48190207..48192286-chr4:48193405..48195580,2	MCF-7	breast:
12	chr4:48227365..48229735-chr4:48239448..48242310,2	K562	blood:
13	chr4:48200101..48201896-chr4:48269773..48271789,2	K562	blood:
14	chr4:48238892..48241068-chr4:48247777..48249287,2	K562	blood:
15	chr4:48211265..48214247-chr4:48216270..48217913,2	K562	blood:
16	chr4:48257479..48259057-chr4:48261577..48263259,2	MCF-7	breast:
17	chr19:40931605..40932510-chr4:48271137..48271845,2	Hela-S3	cervix:
18	chr4:48271855..48272497-chr7:75544014..75544536,2	NB4	blood:
19	chr12:120729424..120730098-chr4:48271378..48272195,2	Hela-S3	cervix:
20	chr4:48274201..48276645-chr4:48276828..48280429,3	K562	blood:
21	chr4:48199323..48202790-chr4:48204123..48207429,4	K562	blood:
22	chr4:48129602..48130429-chr4:48277151..48277985,3	MCF-7	breast:
23	chr4:48242584..48244534-chr4:48245317..48247606,2	K562	blood:
24	chr4:48129433..48130199-chr4:48276992..48278818,4	MCF-7	breast:
25	chr4:48255711..48257883-chr4:48270489..48272038,2	MCF-7	breast:
26	chr4:48204514..48206447-chr4:48263037..48265705,2	K562	blood:
27	chr4:48250701..48254731-chr4:48255352..48259390,5	K562	blood:
28	chr4:48248411..48250691-chr4:48255149..48257827,3	K562	blood:
29	chr4:48264879..48267835-chr4:48269527..48271829,4	K562	blood:
30	chr4:48255521..48259627-chr4:48261501..48267509,10	K562	blood:
31	chr4:48238807..48240507-chr4:48244867..48247720,2	K562	blood:
32	chr4:48239378..48241079-chr4:48271387..48273021,2	MCF-7	breast:
33	chr1:36234965..36235557-chr4:48271368..48271893,2	Hela-S3	cervix:
34	chr4:48247444..48251511-chr4:48269586..48272868,4	K562	blood:
35	chr2:96873932..96874574-chr4:48271406..48272081,2	Hela-S3	cervix:
36	chr4:48260906..48263782-chr4:48270701..48273043,3	K562	blood:
37	chr4:48264189..48268843-chr4:48269527..48273164,9	K562	blood:
38	chr4:48222896..48226335-chr4:48226766..48230334,4	K562	blood:
39	chr4:48253624..48256243-chr4:48267800..48270613,3	MCF-7	breast:
40	chr4:48142752..48143665-chr4:48277017..48277569,2	MCF-7	breast:
41	chr4:48191196..48193426-chr4:48194546..48197180,3	K562	blood:
42	chr4:48191298..48193401-chr4:48269923..48271820,2	K562	blood:
43	chr17:74448509..74449477-chr4:48271558..48272150,2	Hela-S3	cervix:
44	chr4:48238606..48240406-chr4:48242704..48244753,3	K562	blood:
45	chr4:48167349..48169980-chr4:48272046..48273556,2	K562	blood:
46	chr4:48251770..48253352-chr4:48260141..48262130,2	K562	blood:
47	chr4:48231874..48234490-chr4:48252410..48255133,2	K562	blood:
48	chr4:48248411..48250691-chr4:48255149..48257827,3	K562	blood:
49	chr4:48175041..48176757-chr4:48255815..48257585,2	K562	blood:
50	chr4:48214305..48216308-chr4:48218289..48220414,2	K562	blood:

No data

Variant related genes	Relation type
TEC	TF binding region
TEC	CpG island
ENSG00000204685	chromatin interactions
ENSG00000163659	chromatin interactions
ENSG00000265020	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000109171	chromatin interactions
ENSG00000182831	chromatin interactions
ENSG00000127948	chromatin interactions
ENSG00000108312	chromatin interactions
ENSG00000065135	chromatin interactions
ENSG00000092853	chromatin interactions
ENSG00000084090	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000175931	chromatin interactions
ENSG00000197019	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000135605	chromatin interactions
ENSG00000243926	chromatin interactions
ENSG00000145248	chromatin interactions
ENSG00000129673	chromatin interactions

Extended variants
information (count: 3442 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3442 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4695355	chr4:48189710-48189711	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533358872	chr4:48189779-48189780	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551750942	chr4:48189847-48189848	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185348393	chr4:48189924-48189925	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13132499	chr4:48189940-48189941	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555851715	chr4:48189941-48189942	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374251776	chr4:48189989-48189990	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs202090837	chr4:48190052-48190053	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs4694887	chr4:48190096-48190097	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs148687911	chr4:48190113-48190114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs4695356	chr4:48190141-48190142	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs142190236	chr4:48190223-48190224	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs190540167	chr4:48190230-48190231	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs575218586	chr4:48190233-48190234	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs75097005	chr4:48190265-48190266	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs181983559	chr4:48190275-48190276	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs16861106	chr4:48190365-48190366	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541690426	chr4:48190504-48190505	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs559953245	chr4:48190519-48190520	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs559989306	chr4:48190520-48190521	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs79082460	chr4:48190522-48190523	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs183497060	chr4:48190572-48190573	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs552117674	chr4:48190587-48190588	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs573155478	chr4:48190608-48190609	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs569920986	chr4:48190646-48190647	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs371300245	chr4:48190655-48190656	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs188180814	chr4:48190657-48190658	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs541814437	chr4:48190673-48190674	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs141306705	chr4:48190675-48190676	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs551480436	chr4:48190676-48190677	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs561883372	chr4:48190709-48190710	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181062762	chr4:48190758-48190759	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs530893068	chr4:48190772-48190773	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs376785376	chr4:48190777-48190778	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs143667183	chr4:48190885-48190886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566174363	chr4:48190890-48190891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373806971	chr4:48190891-48190892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs28491198	chr4:48190905-48190906	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs115970631	chr4:48190908-48190909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538520802	chr4:48190909-48190910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551971164	chr4:48190950-48190951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369830516	chr4:48191013-48191014	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs146788247	chr4:48191024-48191025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575117694	chr4:48191030-48191031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs536283726	chr4:48191144-48191145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554363306	chr4:48191209-48191210	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572925629	chr4:48191221-48191222	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs540337817	chr4:48191309-48191310	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs17574585	chr4:48191312-48191313	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs77920435	chr4:48191348-48191349	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48158400-48190000	Weak transcription	Aorta	Aorta
2	chr4:48169000-48190000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr4:48175800-48191600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:48178000-48192400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr4:48183200-48194800	Weak transcription	Fetal Thymus	thymus
6	chr4:48185600-48192400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr4:48185800-48189800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:48185800-48197000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:48186000-48194800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr4:48188600-48196000	Weak transcription	Lung	lung
11	chr4:48189400-48189800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:48189400-48190200	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr4:48189400-48190400	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr4:48189600-48189800	Genic enhancers	GM12878-XiMat	blood
15	chr4:48189600-48190000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:48189600-48190200	Enhancers	Primary hematopoietic stem cells	blood
17	chr4:48189600-48190200	Enhancers	Adipose Nuclei	Adipose
18	chr4:48189600-48190200	Enhancers	Fetal Intestine Large	intestine
19	chr4:48189600-48190400	Enhancers	K562	blood
20	chr4:48189600-48190400	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr4:48189600-48190600	Enhancers	Fetal Heart	heart
22	chr4:48189800-48190000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:48189800-48190200	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr4:48189800-48190200	Enhancers	Right Atrium	heart
25	chr4:48189800-48190400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:48189800-48190400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:48189800-48190800	Flanking Active TSS	GM12878-XiMat	blood
28	chr4:48189800-48191200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr4:48190000-48190200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr4:48190000-48190200	Enhancers	Aorta	Aorta
31	chr4:48190000-48190400	Enhancers	Fetal Intestine Small	intestine
32	chr4:48190200-48195200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr4:48190200-48195800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr4:48190400-48191800	Weak transcription	K562	blood
35	chr4:48190400-48194800	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr4:48190400-48195400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:48190400-48195400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:48190400-48197400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr4:48190400-48222000	Weak transcription	Fetal Intestine Small	intestine
40	chr4:48190600-48207200	Weak transcription	Spleen	Spleen
41	chr4:48190800-48191200	Enhancers	GM12878-XiMat	blood
42	chr4:48191200-48191400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr4:48191200-48191800	Genic enhancers	GM12878-XiMat	blood
44	chr4:48191400-48197400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr4:48191800-48192600	Enhancers	K562	blood
46	chr4:48191800-48194000	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
47	chr4:48192400-48192800	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr4:48192400-48193200	Enhancers	Primary B cells from peripheral blood	blood
49	chr4:48192600-48195000	Weak transcription	K562	blood
50	chr4:48192800-48195000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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