Variant report

Variant	esv3395811
Chromosome Location	chr4:56486113-56514675
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:567)
CpG islands
(count:1284)
Chromatin interactive
region (count:20)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56493426-56493494	K562	blood:	n/a	n/a
2	ARID3A	chr4:56501495-56501827	K562	blood:	n/a	n/a
3	ARID3A	chr4:56503388-56504015	K562	blood:	n/a	n/a
4	ATF1	chr4:56501416-56501837	K562	blood:	n/a	n/a
5	ATF1	chr4:56498147-56498454	K562	blood:	n/a	n/a
6	BACH1	chr4:56502324-56502563	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:56502806-56503160	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:56503675-56503978	K562	blood:	n/a	n/a
9	BACH1	chr4:56503593-56503801	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr4:56504145-56504547	K562	blood:	n/a	n/a
11	BHLHE40	chr4:56501226-56501818	K562	blood:	n/a	n/a
12	BHLHE40	chr4:56502266-56502629	K562	blood:	n/a	n/a
13	CBX3	chr4:56504056-56504491	K562	blood:	n/a	n/a
14	CCNT2	chr4:56501265-56503172	K562	blood:	n/a	chr4:56501740-56501760
15	CEBPB	chr4:56500092-56500438	K562	blood:	n/a	n/a
16	CEBPB	chr4:56493262-56493575	K562	blood:	n/a	n/a
17	CEBPB	chr4:56500114-56500405	A549	lung:	n/a	n/a
18	CEBPB	chr4:56498999-56499040	K562	blood:	n/a	n/a
19	CEBPB	chr4:56493333-56493439	A549	lung:	n/a	n/a
20	CEBPB	chr4:56500141-56500429	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:56498129-56498435	K562	blood:	n/a	n/a
22	CEBPB	chr4:56490400-56490597	K562	blood:	n/a	n/a
23	CEBPB	chr4:56500146-56500378	K562	blood:	n/a	n/a
24	CEBPB	chr4:56500041-56500445	K562	blood:	n/a	n/a
25	CEBPB	chr4:56493264-56493488	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:56500139-56500401	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPD	chr4:56500094-56500488	K562	blood:	n/a	n/a
28	CHD1	chr4:56502755-56502917	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr4:56502112-56503096	K562	blood:	n/a	n/a
30	CHD2	chr4:56502183-56502449	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr4:56501652-56502510	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr4:56504399-56504571	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr4:56504383-56504573	K562	blood:	n/a	n/a
34	CTCF	chr4:56504360-56504510	AG09309	skin:	n/a	n/a
35	CTCF	chr4:56504359-56504556	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr4:56502380-56502530	GM12875	blood:	n/a	chr4:56502419-56502432
37	CTCF	chr4:56502380-56502530	HRE	kidney:	n/a	chr4:56502419-56502432
38	CTCF	chr4:56504400-56504550	HPF	lung:	n/a	n/a
39	CTCF	chr4:56502377-56502499	GM10266	blood:	n/a	chr4:56502419-56502432
40	CTCF	chr4:56502360-56502510	SK-N-SH_RA	brain:	n/a	chr4:56502419-56502432
41	CTCF	chr4:56502284-56502549	MCF-7	breast:	n/a	chr4:56502419-56502432
42	CTCF	chr4:56502357-56502493	ProgFib	skin:	n/a	chr4:56502419-56502432
43	CTCF	chr4:56502354-56502525	GM12878	blood:	n/a	chr4:56502419-56502432
44	CTCF	chr4:56504420-56504570	HepG2	liver:	n/a	n/a
45	CTCF	chr4:56504440-56504590	HCT-116	colon:	n/a	n/a
46	CTCF	chr4:56504440-56504590	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr4:56504446-56504539	NHEK	skin:	n/a	n/a
48	CTCF	chr4:56504894-56504928	GM20000	blood:	n/a	n/a
49	CTCF	chr4:56504398-56504579	ProgFib	skin:	n/a	n/a
50	CTCF	chr4:56504412-56504570	LNCaP	prostate:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56502392-56502442	SK-N-SH	brain:	n/a
2	chr4:56502788-56502838	T-47D	breast:	n/a
3	chr4:56502116-56502166	HCT-116	colon:	n/a
4	chr4:56502392-56502442	SK-N-SH	brain:	n/a
5	chr4:56502788-56502838	T-47D	breast:	n/a
6	chr4:56502116-56502166	HCT-116	colon:	n/a
7	chr4:56502544-56502594	Jurkat	blood:	n/a
8	chr4:56502534-56502584	LNCaP	prostate:	n/a
9	chr4:56502544-56502594	HUVEC	blood vessel:	n/a
10	chr4:56500362-56500412	PrEC	prostate:	n/a
11	chr4:56501727-56501777	NH-A	brain:	n/a
12	chr4:56501978-56502028	K562	blood:	n/a
13	chr4:56501727-56501777	SK-N-MC	brain:	n/a
14	chr4:56502898-56502948	HRPEpiC	eye:	n/a
15	chr4:56502849-56502899	PrEC	prostate:	n/a
16	chr4:56502788-56502838	PrEC	prostate:	n/a
17	chr4:56502544-56502594	Caco-2	colon:	n/a
18	chr4:56502469-56502519	GM19239	blood:	n/a
19	chr4:56501718-56501768	AG04450	lung:	fetal
20	chr4:56502849-56502899	SK-N-MC	brain:	n/a
21	chr4:56502849-56502899	SK-N-SH_RA	brain:	n/a
22	chr4:56502788-56502838	HMEC	breast:	n/a
23	chr4:56502598-56502648	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:56502598-56502648	H1-hESC	embryonic stem cell:	embryo
25	chr4:56502116-56502166	NHDF-neo	bronchial:	n/a
26	chr4:56499522-56499572	HepG2	liver:	n/a
27	chr4:56500362-56500412	NB4	blood:	n/a
28	chr4:56496836-56496886	AoSMC	blood vessel:	n/a
29	chr4:56502898-56502948	PANC-1	pancreas:	n/a
30	chr4:56502534-56502584	SK-N-SH_RA	brain:	n/a
31	chr4:56496836-56496886	GM12878	blood:	n/a
32	chr4:56502392-56502442	AG09319	gingival:	n/a
33	chr4:56496836-56496886	T-47D	breast:	n/a
34	chr4:56502898-56502948	ovcar-3	ovarian:	n/a
35	chr4:56502849-56502899	Hela-S3	cervix:	n/a
36	chr4:56502469-56502519	RPTEC	kidney:	n/a
37	chr4:56502116-56502166	AG09309	skin:	n/a
38	chr4:56502116-56502166	SKMC	muscle:	n/a
39	chr4:56504657-56504707	K562	blood:	n/a
40	chr4:56502544-56502594	AG04449	skin:	fetal
41	chr4:56504657-56504707	AG09309	skin:	n/a
42	chr4:56502664-56502714	MCF-7	breast:	n/a
43	chr4:56502864-56502914	MCF-7	breast:	n/a
44	chr4:56502469-56502519	HCPEpiC	choroid plexus:	n/a
45	chr4:56501441-56501491	GM12878	blood:	n/a
46	chr4:56502534-56502584	AG09309	skin:	n/a
47	chr4:56501978-56502028	A549	lung:	n/a
48	chr4:56504657-56504707	IMR90	lung:	fetal
49	chr4:56502664-56502714	AG04450	lung:	fetal
50	chr4:56502116-56502166	GM19239	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:56410839..56413778-chr4:56501227..56505067,4	K562	blood:
2	chr4:56512523..56514282-chr4:56518613..56521303,2	K562	blood:
3	chr4:56469856..56472454-chr4:56489855..56491752,2	K562	blood:
4	chr4:56479641..56481239-chr4:56491828..56493480,2	K562	blood:
5	chr4:56211245..56214093-chr4:56502603..56505420,3	K562	blood:
6	chr4:56500921..56503326-chr4:56505763..56509712,4	K562	blood:
7	chr4:56500129..56502345-chr4:56579313..56582236,2	K562	blood:
8	chr4:56492997..56495090-chr4:56501850..56503549,2	K562	blood:
9	chr4:56492253..56496567-chr4:56500430..56503372,5	K562	blood:
10	chr4:56408119..56414507-chr4:56501105..56505595,8	K562	blood:
11	chr4:56412329..56414161-chr4:56494486..56496762,2	K562	blood:
12	chr4:56407970..56411777-chr4:56498734..56501001,3	K562	blood:
13	chr4:56512381..56514282-chr4:56518613..56520259,2	K562	blood:
14	chr4:56479641..56482011-chr4:56491746..56493328,2	K562	blood:
15	chr4:56500691..56503425-chr4:56513263..56514979,2	K562	blood:
16	chr4:56507649..56509909-chr4:56526051..56528840,3	K562	blood:
17	chr4:56504870..56506522-chr4:56515627..56517625,2	K562	blood:
18	chr4:56503993..56504657-chr4:56601774..56602719,2	MCF-7	breast:
19	chr4:56508010..56509551-chr4:56524906..56527685,2	MCF-7	breast:
20	chr4:56411599..56413538-chr4:56502547..56504625,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMU-2	chr4:56508763-56508927	l_2648_chr4:56499345-56508927_adipose
2	lnc-NMU-1	chr4:56496569-56496627	NONHSAT096475
3	lnc-NMU-1	chr4:56502711-56502865	NONHSAT096475
4	lnc-NMU-2	chr4:56501440-56501555	l_2648_chr4:56499345-56508927_adipose
5	lnc-NMU-2	chr4:56499346-56499878	l_2648_chr4:56499345-56508927_adipose
6	lnc-NMU-1	chr4:56496569-56496629	NONHSAT096476

No data

Variant related genes	Relation type
NMU	TF binding region
NMU	CpG island
ENSG00000272969	chromatin interactions
ENSG00000109255	chromatin interactions
ENSG00000128039	chromatin interactions
ENSG00000134852	chromatin interactions

Extended variants
information (count: 804 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142027901	chr4:56486120-56486121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530930312	chr4:56486140-56486141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548740383	chr4:56486265-56486266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533996763	chr4:56486552-56486553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199821398	chr4:56486558-56486559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558951724	chr4:56486570-56486571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544648099	chr4:56486574-56486575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562456421	chr4:56486612-56486613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370440405	chr4:56486653-56486654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374112150	chr4:56486684-56486685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs367651412	chr4:56486727-56486728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201146909	chr4:56486863-56486864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370288083	chr4:56486895-56486896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374409079	chr4:56486949-56486950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368550269	chr4:56486956-56486957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202107205	chr4:56486978-56486979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372813757	chr4:56487207-56487208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375461532	chr4:56487250-56487251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368385219	chr4:56487278-56487279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372014107	chr4:56487288-56487289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376915425	chr4:56487347-56487348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200462099	chr4:56487362-56487363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200905789	chr4:56487444-56487445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144289701	chr4:56487693-56487694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548231086	chr4:56488101-56488102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200269280	chr4:56488114-56488115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201473145	chr4:56488696-56488697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199775600	chr4:56489410-56489411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200204009	chr4:56489675-56489676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71627120	chr4:56489689-56489690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369526934	chr4:56490107-56490108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371298615	chr4:56490181-56490182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201563796	chr4:56490202-56490203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112357776	chr4:56490208-56490209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567758229	chr4:56490273-56490274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536311021	chr4:56490280-56490281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547234503	chr4:56490310-56490311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567046474	chr4:56490337-56490338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577843017	chr4:56490418-56490419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539373290	chr4:56490426-56490427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559292508	chr4:56490432-56490433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575964746	chr4:56490433-56490434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537860052	chr4:56490444-56490445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200703922	chr4:56490629-56490630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201351986	chr4:56490638-56490639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112471734	chr4:56490769-56490770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111746309	chr4:56490832-56490833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369760081	chr4:56490843-56490844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374094100	chr4:56490848-56490849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531170625	chr4:56490954-56490955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	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
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56473600-56491600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr4:56478200-56491600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:56484200-56491600	Weak transcription	K562	blood
4	chr4:56485200-56487600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:56485200-56491400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:56485400-56491800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr4:56485400-56491800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:56485400-56498000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr4:56485400-56498400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:56489400-56493800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr4:56489400-56498000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:56489800-56498200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:56491400-56492200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:56491600-56492400	ZNF genes & repeats	K562	blood
15	chr4:56491600-56492600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr4:56491600-56496200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:56491800-56492200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr4:56491800-56493400	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr4:56492000-56492200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:56492000-56492200	Enhancers	Esophagus	oesophagus
21	chr4:56492000-56496400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:56492200-56495800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:56492200-56498200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr4:56492200-56498200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr4:56492400-56496600	Strong transcription	K562	blood
26	chr4:56492600-56498400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr4:56493400-56500200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr4:56493800-56494600	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr4:56494000-56500600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr4:56494600-56495200	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr4:56495200-56496200	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr4:56495800-56499000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:56496200-56498200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr4:56496200-56498800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr4:56496600-56497000	Transcr. at gene 5' and 3'	K562	blood
36	chr4:56497000-56498000	Active TSS	K562	blood
37	chr4:56498000-56498600	Transcr. at gene 5' and 3'	K562	blood
38	chr4:56498000-56499000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr4:56498000-56500200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr4:56498200-56498600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr4:56498200-56498800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:56498200-56499000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr4:56498200-56499200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:56498200-56499800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:56498400-56499200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:56498400-56499600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:56498600-56499000	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr4:56498600-56499600	Active TSS	K562	blood
49	chr4:56498800-56499800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:56498800-56500000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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