Variant report

Variant	esv3389909
Chromosome Location	chr4:670502-673300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:367)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:671719-672186	GM12878	blood:	n/a	n/a
2	BHLHE40	chr4:671777-672089	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:669804-670628	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:669929-670601	GM12878	blood:	n/a	n/a
5	CCNT2	chr4:671759-671983	K562	blood:	n/a	n/a
6	CEBPB	chr4:671490-671511	HepG2	liver:	n/a	n/a
7	CHD2	chr4:672314-672478	HepG2	liver:	n/a	n/a
8	CHD2	chr4:671811-672077	GM12878	blood:	n/a	n/a
9	CHD2	chr4:671532-671607	HepG2	liver:	n/a	n/a
10	CTCF	chr4:671861-672025	GM19239	blood:	n/a	n/a
11	CTCF	chr4:671808-671996	NHEK	skin:	n/a	n/a
12	CTCF	chr4:670788-670838	GM19239	blood:	n/a	n/a
13	CTCF	chr4:673260-673410	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr4:670420-670570	GM12873	blood:	n/a	n/a
15	CTCF	chr4:671857-671859	GM19239	blood:	n/a	n/a
16	CTCF	chr4:670354-670569	GM19239	blood:	n/a	n/a
17	EBF1	chr4:669615-670857	GM12878	blood:	n/a	chr4:670830-670839 chr4:670724-670734
18	EBF1	chr4:671665-671780	GM12878	blood:	n/a	chr4:671678-671687 chr4:671677-671687 chr4:671676-671687
19	EGR1	chr4:671517-672443	HCT-116	colon:	n/a	chr4:672267-672280
20	EGR1	chr4:671653-672123	ECC-1	luminal epithelium:	n/a	n/a
21	EGR1	chr4:671719-672021	K562	blood:	n/a	n/a
22	EGR1	chr4:671434-672410	HCT-116	colon:	n/a	chr4:672267-672280
23	EGR1	chr4:671628-672173	ECC-1	luminal epithelium:	n/a	n/a
24	EGR1	chr4:671767-672004	K562	blood:	n/a	n/a
25	ELF1	chr4:670473-671133	GM12878	blood:	n/a	n/a
26	EP300	chr4:671827-672125	GM12878	blood:	n/a	n/a
27	EP300	chr4:671770-672103	GM12878	blood:	n/a	n/a
28	EP300	chr4:671891-672063	HepG2	liver:	n/a	n/a
29	EP300	chr4:670810-670912	GM12878	blood:	n/a	chr4:670889-670905
30	EP300	chr4:669810-670514	GM12878	blood:	n/a	n/a
31	FOS	chr4:671559-671762	MCF10A-Er-Src	breast:	n/a	chr4:671632-671642 chr4:671632-671642
32	FOS	chr4:671502-671949	MCF10A-Er-Src	breast:	n/a	chr4:671632-671642 chr4:671632-671642
33	FOS	chr4:671505-671825	MCF10A-Er-Src	breast:	n/a	chr4:671632-671642 chr4:671632-671642
34	FOS	chr4:671508-671979	MCF10A-Er-Src	breast:	n/a	chr4:671632-671642 chr4:671632-671642
35	FOSL2	chr4:671361-672084	HepG2	liver:	n/a	chr4:671632-671642 chr4:671632-671642
36	FOXA1	chr4:671615-672100	HepG2	liver:	n/a	n/a
37	FOXA2	chr4:671740-672047	HepG2	liver:	n/a	n/a
38	FOXM1	chr4:669787-670502	GM12878	blood:	n/a	n/a
39	HEY1	chr4:671442-672059	HepG2	liver:	n/a	n/a
40	HMGN3	chr4:670239-670562	K562	blood:	n/a	n/a
41	HMGN3	chr4:672888-673242	K562	blood:	n/a	n/a
42	HMGN3	chr4:672174-672291	K562	blood:	n/a	n/a
43	JUND	chr4:671465-671725	HepG2	liver:	n/a	chr4:671632-671642 chr4:671631-671642 chr4:671632-671642
44	MAX	chr4:671600-672148	ECC-1	luminal epithelium:	n/a	n/a
45	MAX	chr4:671586-672116	ECC-1	luminal epithelium:	n/a	chr4:671595-671605
46	MAX	chr4:671524-672466	HepG2	liver:	n/a	chr4:671595-671605
47	MAX	chr4:671594-672111	MCF-7	breast:	n/a	chr4:671595-671605
48	MAX	chr4:671759-672057	GM12878	blood:	n/a	n/a
49	MAX	chr4:671630-672095	HepG2	liver:	n/a	n/a
50	MAZ	chr4:671713-671913	HepG2	liver:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:670694-670744	HEK293	kidney:	embryo
2	chr4:670694-670744	HEK293	kidney:	embryo
3	chr4:670694-670744	SKMC	muscle:	n/a
4	chr4:671543-671593	Caco-2	colon:	n/a
5	chr4:671543-671593	Jurkat	blood:	n/a
6	chr4:671851-671901	BE2_C	brain:	n/a
7	chr4:671851-671901	GM06990	blood:	n/a
8	chr4:671791-671841	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:671791-671841	GM12891	blood:	n/a
10	chr4:670694-670744	HL-60	blood:	n/a
11	chr4:671489-671539	HCM	heart:	n/a
12	chr4:671550-671600	HL-60	blood:	n/a
13	chr4:671489-671539	AG09309	skin:	n/a
14	chr4:671550-671600	PFSK-1	brain:	n/a
15	chr4:671851-671901	RPTEC	kidney:	n/a
16	chr4:670694-670744	ECC-1	luminal epithelium:	n/a
17	chr4:671489-671539	NHBE	bronchial:	n/a
18	chr4:670694-670744	GM12891	blood:	n/a
19	chr4:671791-671841	AG09309	skin:	n/a
20	chr4:670694-670744	SK-N-SH	brain:	n/a
21	chr4:671851-671901	NHBE	bronchial:	n/a
22	chr4:671550-671600	HUVEC	blood vessel:	n/a
23	chr4:671489-671539	BJ	skin:	n/a
24	chr4:671851-671901	SKMC	muscle:	n/a
25	chr4:671791-671841	K562	blood:	n/a
26	chr4:671791-671841	GM12892	blood:	n/a
27	chr4:671543-671593	ovcar-3	ovarian:	n/a
28	chr4:671543-671593	HepG2	liver:	n/a
29	chr4:671851-671901	GM12892	blood:	n/a
30	chr4:671489-671539	Hela-S3	cervix:	n/a
31	chr4:671489-671539	HEEpiC	esophagus:	n/a
32	chr4:670694-670744	H1-hESC	embryonic stem cell:	embryo
33	chr4:671489-671539	A549	lung:	n/a
34	chr4:671791-671841	ProgFib	skin:	n/a
35	chr4:671791-671841	SK-N-SH	brain:	n/a
36	chr4:671851-671901	AoSMC	blood vessel:	n/a
37	chr4:671489-671539	HIPEpiC	eye:	n/a
38	chr4:671791-671841	H1-hESC	embryonic stem cell:	embryo
39	chr4:671791-671841	AoSMC	blood vessel:	n/a
40	chr4:671543-671593	HEK293	kidney:	embryo
41	chr4:671489-671539	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:670694-670744	A549	lung:	n/a
43	chr4:671489-671539	CMK	blood:	n/a
44	chr4:671851-671901	SK-N-SH_RA	brain:	n/a
45	chr4:671550-671600	NHDF-neo	bronchial:	n/a
46	chr4:671851-671901	PFSK-1	brain:	n/a
47	chr4:671550-671600	SK-N-SH_RA	brain:	n/a
48	chr4:670694-670744	BJ	skin:	n/a
49	chr4:671851-671901	LNCaP	prostate:	n/a
50	chr4:671791-671841	LNCaP	prostate:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:666292..671732-chr4:694079..701503,8	MCF-7	breast:
2	chr4:666295..671517-chr4:698228..703248,8	MCF-7	breast:
3	chr4:596138..597128-chr4:673282..674051,3	MCF-7	breast:
4	chr4:671080..676330-chr4:771868..776883,7	K562	blood:
5	chr4:658187..662144-chr4:672176..676426,5	MCF-7	breast:
6	chr4:672883..676399-chr4:697081..701106,5	MCF-7	breast:
7	chr4:491399..494814-chr4:670516..673656,5	K562	blood:
8	chr4:669988..672792-chr4:681146..683044,2	K562	blood:
9	chr4:493062..494777-chr4:668037..670861,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE6B-2	chr4:668129-671710	NONHSAT094599

No data

Variant related genes	Relation type
MYL5	TF binding region
ATP5I	TF binding region
MYL5	CpG island
ATP5I	CpG island
ENSG00000133256	chromatin interactions
ENSG00000182903	chromatin interactions
ENSG00000169026	chromatin interactions
ENSG00000249592	chromatin interactions
ENSG00000185619	chromatin interactions
ENSG00000174227	chromatin interactions

Extended variants
information (count: 154 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:154 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377599754	chr4:670570-670571	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
2	rs551232879	chr4:670574-670575	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
3	rs111561980	chr4:670575-670576	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
4	rs564164349	chr4:670622-670623	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
5	rs117211311	chr4:670671-670672	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
6	rs531767447	chr4:670734-670735	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
7	rs74551323	chr4:670742-670743	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
8	rs374667350	chr4:670810-670811	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
9	rs550420208	chr4:670829-670830	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
10	rs114450750	chr4:670830-670831	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	mRNA abundance
11	rs529651731	chr4:670843-670844	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
12	rs547791760	chr4:670861-670862	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
13	rs184187611	chr4:670895-670896	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
14	rs539914399	chr4:670896-670897	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
15	rs557931350	chr4:670904-670905	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
16	rs570136571	chr4:670907-670908	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
17	rs536816147	chr4:670935-670936	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
18	rs372771412	chr4:671021-671022	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
19	rs190185025	chr4:671044-671045	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
20	rs573581464	chr4:671071-671072	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
21	rs181288147	chr4:671100-671101	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
22	rs540952644	chr4:671156-671157	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
23	rs552544347	chr4:671204-671205	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
24	rs184913645	chr4:671225-671226	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
25	rs544993870	chr4:671262-671263	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
26	rs370656710	chr4:671266-671267	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
27	rs530648827	chr4:671274-671275	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
28	rs544018125	chr4:671286-671287	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
29	rs74905711	chr4:671296-671297	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
30	rs79782649	chr4:671344-671345	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
31	rs530082190	chr4:671356-671357	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
32	rs536118051	chr4:671444-671445	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs548151155	chr4:671483-671484	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
34	rs566373409	chr4:671487-671488	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
35	rs115100853	chr4:671522-671523	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
36	rs373085220	chr4:671543-671544	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
37	rs117608218	chr4:671548-671549	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs568870850	chr4:671550-671551	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
39	rs539438274	chr4:671551-671552	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
40	rs537182180	chr4:671635-671636	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
41	rs555118733	chr4:671641-671642	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
42	rs189373304	chr4:671670-671671	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
43	rs371064913	chr4:671679-671680	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
44	rs552805959	chr4:671722-671723	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs577893306	chr4:671723-671724	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs375196584	chr4:671750-671751	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs368446750	chr4:671779-671780	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs200903251	chr4:671782-671783	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs375255290	chr4:671791-671792	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs199897367	chr4:671792-671793	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	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
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Type 2 diabetes	21754918	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:668600-670800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
2	chr4:668800-670600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:668800-670800	Flanking Active TSS	GM12878-XiMat	blood
4	chr4:668800-671200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr4:668800-674400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr4:669000-672200	Enhancers	Spleen	Spleen
7	chr4:669200-670600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:669200-670800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:669200-671000	Enhancers	Fetal Heart	heart
10	chr4:669200-671000	Enhancers	Fetal Thymus	thymus
11	chr4:669200-671200	Enhancers	Placenta Amnion	Placenta Amnion
12	chr4:669200-671400	Enhancers	Primary B cells from peripheral blood	blood
13	chr4:669200-672000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:669200-672600	Enhancers	Esophagus	oesophagus
15	chr4:669200-672600	Enhancers	Fetal Intestine Large	intestine
16	chr4:669200-673000	Enhancers	Pancreas	Pancrea
17	chr4:669200-674200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:669200-674400	Weak transcription	Fetal Lung	lung
19	chr4:669400-670600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr4:669400-670600	Genic enhancers	Fetal Intestine Small	intestine
21	chr4:669400-670600	Enhancers	K562	blood
22	chr4:669400-671000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr4:669400-671200	Enhancers	Primary B cells from cord blood	blood
24	chr4:669400-671400	Enhancers	Psoas Muscle	Psoas
25	chr4:669400-672200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:669400-672800	Enhancers	Duodenum Mucosa	Duodenum
27	chr4:669400-674000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr4:669400-674200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr4:669400-674200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr4:669400-674200	Weak transcription	NH-A	brain
31	chr4:669400-674400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr4:669400-674400	Weak transcription	Ovary	ovary
33	chr4:669400-674400	Weak transcription	Right Atrium	heart
34	chr4:669400-674600	Enhancers	Placenta	Placenta
35	chr4:669400-674600	Weak transcription	HUVEC	blood vessel
36	chr4:669600-670600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr4:669600-670800	Weak transcription	Colonic Mucosa	Colon
38	chr4:669600-671000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:669600-671000	Weak transcription	HMEC	breast
40	chr4:669600-671400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:669600-671400	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:669600-671600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr4:669600-671800	Weak transcription	Brain Cingulate Gyrus	brain
44	chr4:669600-673800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr4:669600-674000	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr4:669600-674000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr4:669600-674000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr4:669600-674000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:669600-674000	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr4:669600-674200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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