Variant report

Variant	nsv593439
Chromosome Location	chr4:3149016-3215835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:764)
CpG islands
(count:671)
Chromatin interactive
region (count:53)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3205836-3206113	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:3195585-3195876	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:3207818-3208171	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:3209205-3209827	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:3195609-3195853	K562	blood:	n/a	n/a
6	ARID3A	chr4:3204979-3205518	HepG2	liver:	n/a	n/a
7	ATF1	chr4:3204044-3204523	K562	blood:	n/a	n/a
8	ATF2	chr4:3169679-3170048	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:3204107-3204572	GM12878	blood:	n/a	n/a
10	BATF	chr4:3203757-3204345	GM12878	blood:	n/a	chr4:3203937-3203947
11	BATF	chr4:3191233-3191533	GM12878	blood:	n/a	n/a
12	BCL3	chr4:3181057-3181672	GM12878	blood:	n/a	n/a
13	BCL3	chr4:3180992-3181755	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:3203779-3204482	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:3204704-3204807	GM12878	blood:	n/a	n/a
16	BRCA1	chr4:3203534-3203615	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr4:3204172-3204363	GM12878	blood:	n/a	n/a
18	CBX3	chr4:3171037-3171318	K562	blood:	n/a	n/a
19	CEBPB	chr4:3201961-3201963	A549	lung:	n/a	n/a
20	CEBPB	chr4:3204885-3206019	HepG2	liver:	n/a	chr4:3205402-3205413 chr4:3205404-3205415 chr4:3205670-3205681
21	CEBPB	chr4:3211969-3212213	A549	lung:	n/a	n/a
22	CEBPB	chr4:3211957-3212234	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:3209275-3209643	HepG2	liver:	n/a	chr4:3209463-3209476 chr4:3209547-3209559
24	CEBPB	chr4:3183653-3183937	HepG2	liver:	n/a	chr4:3183790-3183801 chr4:3183790-3183803 chr4:3183742-3183753 chr4:3183791-3183802
25	CEBPB	chr4:3207814-3208014	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:3209298-3209675	HepG2	liver:	n/a	chr4:3209463-3209476 chr4:3209547-3209559
27	CEBPB	chr4:3183625-3183943	A549	lung:	n/a	chr4:3183790-3183801 chr4:3183790-3183803 chr4:3183742-3183753 chr4:3183791-3183802
28	CEBPB	chr4:3183605-3183968	IMR90	lung:	n/a	chr4:3183790-3183801 chr4:3183790-3183803 chr4:3183742-3183753 chr4:3183791-3183802
29	CEBPB	chr4:3183735-3183935	K562	blood:	n/a	chr4:3183790-3183801 chr4:3183790-3183803 chr4:3183742-3183753 chr4:3183791-3183802
30	CEBPB	chr4:3205814-3206027	A549	lung:	n/a	n/a
31	CEBPB	chr4:3155229-3155337	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:3180903-3181312	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:3209306-3209598	Hela-S3	cervix:	n/a	chr4:3209463-3209476 chr4:3209547-3209559
34	CEBPB	chr4:3201982-3202075	HepG2	liver:	n/a	chr4:3202000-3202013 chr4:3202001-3202012
35	CEBPB	chr4:3205266-3206224	IMR90	lung:	n/a	chr4:3205402-3205413 chr4:3205404-3205415 chr4:3205670-3205681
36	CEBPB	chr4:3162179-3162380	K562	blood:	n/a	chr4:3162360-3162372
37	CEBPB	chr4:3193674-3193741	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:3209280-3209629	HepG2	liver:	n/a	chr4:3209463-3209476 chr4:3209547-3209559
39	CEBPB	chr4:3209353-3209578	HepG2	liver:	n/a	chr4:3209463-3209476 chr4:3209547-3209559
40	CEBPD	chr4:3207750-3208031	HepG2	liver:	n/a	n/a
41	CHD1	chr4:3203977-3204436	GM12878	blood:	n/a	n/a
42	CHD2	chr4:3203779-3204448	GM12878	blood:	n/a	n/a
43	CHD2	chr4:3204709-3204925	GM12878	blood:	n/a	n/a
44	CREB1	chr4:3209057-3209783	HepG2	liver:	n/a	n/a
45	CTCF	chr4:3153080-3153230	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr4:3195627-3195827	Lung_OC	lung:	n/a	chr4:3195724-3195742 chr4:3195728-3195735 chr4:3195726-3195747 chr4:3195725-3195741
47	CTCF	chr4:3153136-3153261	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:3153100-3153250	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:3209241-3209392	HepG2	liver:	n/a	chr4:3209319-3209328
50	CTCF	chr4:3199880-3200030	GM12866	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3193868-3193918	HEK293	kidney:	embryo
2	chr4:3170095-3170145	HAEpiC	amniotic membrane:	n/a
3	chr4:3208354-3208404	U87	brain:	n/a
4	chr4:3170095-3170145	AG09319	gingival:	n/a
5	chr4:3204792-3204842	HRE	kidney:	n/a
6	chr4:3170095-3170145	T-47D	breast:	n/a
7	chr4:3204792-3204842	ovcar-3	ovarian:	n/a
8	chr4:3180930-3180980	AG04450	lung:	fetal
9	chr4:3180930-3180980	U87	brain:	n/a
10	chr4:3170095-3170145	AG04449	skin:	fetal
11	chr4:3204792-3204842	NHDF-neo	bronchial:	n/a
12	chr4:3208330-3208380	AoSMC	blood vessel:	n/a
13	chr4:3170095-3170145	SK-N-SH	brain:	n/a
14	chr4:3204792-3204842	HEK293	kidney:	embryo
15	chr4:3204843-3204893	Hepatocyte	liver:	n/a
16	chr4:3204843-3204893	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:3170095-3170145	ovcar-3	ovarian:	n/a
18	chr4:3208330-3208380	AG09319	gingival:	n/a
19	chr4:3204792-3204842	PrEC	prostate:	n/a
20	chr4:3208589-3208639	MCF10A-Er-Src	breast:	n/a
21	chr4:3203982-3204032	ECC-1	luminal epithelium:	n/a
22	chr4:3208354-3208404	Hepatocyte	liver:	n/a
23	chr4:3208589-3208639	Caco-2	colon:	n/a
24	chr4:3208354-3208404	HCT-116	colon:	n/a
25	chr4:3208330-3208380	SKMC	muscle:	n/a
26	chr4:3208354-3208404	SK-N-SH_RA	brain:	n/a
27	chr4:3193868-3193918	HUVEC	blood vessel:	n/a
28	chr4:3208354-3208404	HPAEpiC	pulmonary alveolar:	n/a
29	chr4:3208678-3208728	HCM	heart:	n/a
30	chr4:3193868-3193918	GM12891	blood:	n/a
31	chr4:3208354-3208404	HL-60	blood:	n/a
32	chr4:3170095-3170145	Caco-2	colon:	n/a
33	chr4:3208330-3208380	MCF-7	breast:	n/a
34	chr4:3170095-3170145	HUVEC	blood vessel:	n/a
35	chr4:3204843-3204893	NHBE	bronchial:	n/a
36	chr4:3208678-3208728	GM12892	blood:	n/a
37	chr4:3208678-3208728	U87	brain:	n/a
38	chr4:3204843-3204893	H1-hESC	embryonic stem cell:	embryo
39	chr4:3208589-3208639	HIPEpiC	eye:	n/a
40	chr4:3204843-3204893	HUVEC	blood vessel:	n/a
41	chr4:3204843-3204893	AG04449	skin:	fetal
42	chr4:3204843-3204893	HIPEpiC	eye:	n/a
43	chr4:3208678-3208728	HRPEpiC	eye:	n/a
44	chr4:3208678-3208728	HEK293	kidney:	embryo
45	chr4:3208330-3208380	HIPEpiC	eye:	n/a
46	chr4:3208678-3208728	HNPCEpiC	eye:	n/a
47	chr4:3204792-3204842	HUVEC	blood vessel:	n/a
48	chr4:3204843-3204893	HCM	heart:	n/a
49	chr4:3208354-3208404	LNCaP	prostate:	n/a
50	chr4:3203982-3204032	NT2-D1	testis:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3198767..3201589-chr4:3205196..3207411,2	K562	blood:
2	chr4:3210706..3212458-chr4:3214564..3216514,2	MCF-7	breast:
3	chr4:3206891..3208682-chr4:3463951..3466139,2	MCF-7	breast:
4	chr4:3110448..3112382-chr4:3193670..3195664,2	MCF-7	breast:
5	chr4:3150389..3152332-chr4:3155946..3158430,2	K562	blood:
6	chr4:3137167..3139741-chr4:3151694..3153218,2	K562	blood:
7	chr4:3196534..3198445-chr4:3199145..3202681,3	MCF-7	breast:
8	chr4:3115797..3118654-chr4:3180126..3182522,2	MCF-7	breast:
9	chr4:3200457..3202229-chr4:3205409..3207674,2	K562	blood:
10	chr4:3169372..3171758-chr4:3194914..3197788,2	K562	blood:
11	chr4:3212742..3214641-chr4:3244184..3246248,2	K562	blood:
12	chr4:3195364..3197169-chr4:3200339..3201843,2	K562	blood:
13	chr4:3198767..3201589-chr4:3205196..3207411,2	K562	blood:
14	chr4:3195952..3197606-chr4:3265003..3267231,2	K562	blood:
15	chr4:3195267..3196266-chr4:3444903..3445887,5	MCF-7	breast:
16	chr4:3200457..3202229-chr4:3205409..3207674,2	K562	blood:
17	chr4:3215167..3215891-chr4:3479590..3480357,2	K562	blood:
18	chr4:3202805..3205724-chr4:3208836..3211288,3	K562	blood:
19	chr4:3213994..3215627-chr4:3278478..3280944,2	MCF-7	breast:
20	chr4:3196724..3198622-chr4:3198822..3201545,2	MCF-7	breast:
21	chr4:3168550..3170092-chr4:3179399..3181924,2	MCF-7	breast:
22	chr4:3204224..3206144-chr4:3208836..3210457,2	K562	blood:
23	chr4:3142213..3145197-chr4:3147789..3149638,3	MCF-7	breast:
24	chr4:3174198..3176315-chr4:3186979..3189663,2	K562	blood:
25	chr4:3209550..3212168-chr4:3442496..3445416,2	MCF-7	breast:
26	chr4:3116172..3119060-chr4:3178746..3180819,2	K562	blood:
27	chr4:3213644..3215707-chr4:3250589..3252693,2	MCF-7	breast:
28	chr4:3210706..3212458-chr4:3214564..3216514,2	MCF-7	breast:
29	chr4:3201399..3203934-chr4:3207301..3210126,2	MCF-7	breast:
30	chr4:3190288..3192696-chr4:3294667..3296628,2	K562	blood:
31	chr4:3214912..3216884-chr4:3292944..3295719,2	MCF-7	breast:
32	chr4:3173185..3175409-chr4:3176697..3178512,2	MCF-7	breast:
33	chr4:3196534..3198445-chr4:3199145..3202681,3	MCF-7	breast:
34	chr4:3195364..3197169-chr4:3200339..3201843,2	K562	blood:
35	chr4:3196724..3198622-chr4:3198822..3201545,2	MCF-7	breast:
36	chr4:3158228..3160226-chr4:3168237..3170357,2	K562	blood:
37	chr4:3187730..3190882-chr4:3194133..3197164,3	K562	blood:
38	chr4:3045756..3048472-chr4:3209114..3211020,2	K562	blood:
39	chr4:3158228..3160226-chr4:3168237..3170357,2	K562	blood:
40	chr4:3112733..3115394-chr4:3157286..3160905,3	MCF-7	breast:
41	chr4:3168255..3170056-chr4:3176089..3177701,2	K562	blood:
42	chr4:3150389..3152332-chr4:3155946..3158430,2	K562	blood:
43	chr4:3174198..3176315-chr4:3186979..3189663,2	K562	blood:
44	chr4:3168255..3170056-chr4:3176089..3177701,2	K562	blood:
45	chr4:3169372..3171758-chr4:3194914..3197788,2	K562	blood:
46	chr4:3110166..3112749-chr4:3184867..3187670,2	MCF-7	breast:
47	chr4:3192746..3194310-chr4:3485907..3488354,2	MCF-7	breast:
48	chr4:3187730..3190882-chr4:3194133..3197164,3	K562	blood:
49	chr4:3201399..3203934-chr4:3207301..3210126,2	MCF-7	breast:
50	chr4:3213997..3215990-chr4:3485524..3487678,2	MCF-7	breast:

No data

Variant related genes	Relation type
HTT	TF binding region
HTT	CpG island
ENSG00000197386	chromatin interactions
ENSG00000249673	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000188981	chromatin interactions
ENSG00000109736	chromatin interactions
ENSG00000199335	chromatin interactions
ENSG00000159788	chromatin interactions
ENSG00000109758	chromatin interactions

Extended variants
information (count: 2748 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs363102	chr4:3149016-3149017	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145600850	chr4:3149040-3149041	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111603953	chr4:3149041-3149042	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565093022	chr4:3149043-3149044	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144370512	chr4:3149052-3149053	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183216366	chr4:3149056-3149057	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568989755	chr4:3149065-3149066	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148909465	chr4:3149108-3149109	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532916340	chr4:3149111-3149112	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3025845	chr4:3149127-3149128	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566520040	chr4:3149182-3149183	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549051398	chr4:3149199-3149200	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565963374	chr4:3149216-3149217	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545222741	chr4:3149234-3149235	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80044337	chr4:3149257-3149258	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs3025844	chr4:3149291-3149292	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs187866010	chr4:3149313-3149314	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537570388	chr4:3149321-3149322	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557411471	chr4:3149331-3149332	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567592213	chr4:3149373-3149374	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191087324	chr4:3149404-3149405	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146273410	chr4:3149467-3149468	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573208557	chr4:3149476-3149477	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs57777947	chr4:3149483-3149484	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182386041	chr4:3149559-3149560	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558746126	chr4:3149638-3149639	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112095365	chr4:3149664-3149665	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147879252	chr4:3149674-3149675	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372346894	chr4:3149694-3149695	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200353055	chr4:3149700-3149701	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543150172	chr4:3149713-3149714	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201365651	chr4:3149723-3149724	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374733848	chr4:3149745-3149746	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529839694	chr4:3149777-3149778	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1065747	chr4:3149780-3149781	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371584472	chr4:3149782-3149783	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376205282	chr4:3149790-3149791	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542613235	chr4:3149831-3149832	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369374727	chr4:3149839-3149840	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200581635	chr4:3149844-3149845	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374106761	chr4:3149862-3149863	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528411716	chr4:3149868-3149869	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377680756	chr4:3149898-3149899	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373038776	chr4:3149899-3149900	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369912429	chr4:3149906-3149907	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377592444	chr4:3149929-3149930	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147061837	chr4:3149975-3149976	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148122353	chr4:3150015-3150016	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187906805	chr4:3150064-3150065	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530713978	chr4:3150078-3150079	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
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
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:2573 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3088200-3164200	Strong transcription	Primary monocytes fromperipheralblood	blood
2	chr4:3097200-3162200	Strong transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:3097400-3163800	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:3098000-3162600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:3100000-3159400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:3108600-3163000	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr4:3108800-3164600	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr4:3114600-3292400	Weak transcription	Right Atrium	heart
9	chr4:3114800-3162800	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr4:3115800-3161600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:3115800-3162800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr4:3125200-3163000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:3125200-3163200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr4:3126800-3164400	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr4:3127000-3164400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:3127200-3152600	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr4:3127200-3157200	Strong transcription	Sigmoid Colon	Sigmoid Colon
18	chr4:3127200-3163400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:3127200-3163400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr4:3127200-3163400	Strong transcription	Fetal Muscle Trunk	muscle
21	chr4:3127200-3163600	Strong transcription	Fetal Intestine Large	intestine
22	chr4:3127200-3164200	Strong transcription	Fetal Muscle Leg	muscle
23	chr4:3127200-3164400	Strong transcription	Primary B cells from peripheral blood	blood
24	chr4:3131200-3162600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr4:3133400-3155000	Weak transcription	Fetal Heart	heart
26	chr4:3134800-3162000	Weak transcription	Hela-S3	cervix
27	chr4:3136400-3149400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:3136400-3149400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:3136400-3151400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:3136600-3156000	Weak transcription	Stomach Mucosa	stomach
31	chr4:3137800-3163400	Strong transcription	Liver	Liver
32	chr4:3139600-3164800	Strong transcription	Duodenum Mucosa	Duodenum
33	chr4:3142600-3149600	Weak transcription	Fetal Brain Male	brain
34	chr4:3144200-3161800	Strong transcription	GM12878-XiMat	blood
35	chr4:3144400-3151400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:3144600-3159400	Strong transcription	Osteobl	bone
37	chr4:3145400-3153600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr4:3145400-3156600	Strong transcription	Left Ventricle	heart
39	chr4:3145600-3152400	Strong transcription	Placenta Amnion	Placenta Amnion
40	chr4:3145600-3164600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr4:3145800-3164000	Strong transcription	Adipose Nuclei	Adipose
42	chr4:3145800-3239200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr4:3146000-3153600	Strong transcription	HUVEC	blood vessel
44	chr4:3146000-3159600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr4:3146000-3163400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:3146000-3163600	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr4:3146200-3152800	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr4:3146200-3156400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr4:3146200-3162600	Strong transcription	Brain Hippocampus Middle	brain
50	chr4:3146200-3163400	Strong transcription	Skeletal Muscle Male	skeletal muscle

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