Variant report

Variant	nsv870141
Chromosome Location	chr4:2982146-3021346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3015778-3015920	K562	blood:	n/a	n/a
2	ARID3A	chr4:3011076-3011449	K562	blood:	n/a	n/a
3	ARID3A	chr4:3011066-3011492	HepG2	liver:	n/a	n/a
4	ATF2	chr4:3015423-3015901	GM12878	blood:	n/a	n/a
5	ATF2	chr4:3015373-3015930	GM12878	blood:	n/a	n/a
6	BATF	chr4:3015475-3015900	GM12878	blood:	n/a	n/a
7	BATF	chr4:3015443-3016179	GM12878	blood:	n/a	n/a
8	BATF	chr4:3011731-3011987	GM12878	blood:	n/a	chr4:3011910-3011920
9	BCLAF1	chr4:3015405-3015854	GM12878	blood:	n/a	n/a
10	BCLAF1	chr4:3015426-3016050	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:3021146-3021444	GM12878	blood:	n/a	chr4:3021209-3021218 chr4:3021209-3021218 chr4:3021208-3021217
12	BHLHE40	chr4:3015440-3015913	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:3015794-3016042	K562	blood:	n/a	n/a
14	BHLHE40	chr4:3011876-3011946	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:3011155-3011372	GM12878	blood:	n/a	n/a
16	CBX3	chr4:2982837-2983462	K562	blood:	n/a	n/a
17	CBX3	chr4:2982906-2983436	K562	blood:	n/a	n/a
18	CCNT2	chr4:3015769-3015968	K562	blood:	n/a	chr4:3015904-3015924
19	CEBPB	chr4:3012680-3013191	Hela-S3	cervix:	n/a	chr4:3013009-3013020
20	CEBPB	chr4:3012845-3013172	HepG2	liver:	n/a	chr4:3013009-3013020
21	CEBPB	chr4:3011636-3012059	Hela-S3	cervix:	n/a	chr4:3011874-3011887 chr4:3011875-3011887
22	CEBPB	chr4:2990520-2990621	K562	blood:	n/a	n/a
23	CEBPB	chr4:3012707-3013199	IMR90	lung:	n/a	chr4:3013009-3013020
24	CEBPB	chr4:3011198-3011910	HepG2	liver:	n/a	chr4:3011874-3011887 chr4:3011875-3011887
25	CEBPB	chr4:3011669-3011942	A549	lung:	n/a	chr4:3011874-3011887 chr4:3011875-3011887
26	CEBPD	chr4:3015790-3016098	K562	blood:	n/a	n/a
27	CEBPD	chr4:3015770-3016134	K562	blood:	n/a	n/a
28	CHD2	chr4:3015570-3015700	GM12878	blood:	n/a	n/a
29	CREB1	chr4:3011599-3012024	GM12878	blood:	n/a	chr4:3011632-3011645
30	CREB1	chr4:3011607-3012017	GM12878	blood:	n/a	chr4:3011632-3011645
31	CTCF	chr4:3011200-3011350	SK-N-SH_RA	brain:	n/a	chr4:3011208-3011221
32	CTCF	chr4:3011140-3011290	HMEC	breast:	n/a	chr4:3011208-3011221
33	CTCF	chr4:3011200-3011350	NHEK	skin:	n/a	chr4:3011208-3011221
34	CTCF	chr4:3011160-3011310	GM12870	blood:	n/a	chr4:3011208-3011221
35	CTCF	chr4:3011113-3011117	LNCaP	prostate:	n/a	n/a
36	CTCF	chr4:3011220-3011370	HVMF	connective:	n/a	n/a
37	CTCF	chr4:3011220-3011370	K562	blood:	n/a	n/a
38	CTCF	chr4:3011200-3011350	WERI-Rb-1	eye:	n/a	chr4:3011208-3011221
39	CTCF	chr4:3011200-3011350	HRE	kidney:	n/a	chr4:3011208-3011221
40	CTCF	chr4:3011180-3011330	K562	blood:	n/a	chr4:3011208-3011221
41	CTCF	chr4:3011160-3011310	HCPEpiC	choroid plexus:	n/a	chr4:3011208-3011221
42	CTCF	chr4:3011160-3011310	HVMF	connective:	n/a	chr4:3011208-3011221
43	CTCF	chr4:3011140-3011290	HA-sp	spinal cord:	n/a	chr4:3011208-3011221
44	CTCF	chr4:3011133-3011323	GM19240	blood:	n/a	chr4:3011208-3011221
45	CTCF	chr4:3011097-3011377	K562	blood:	n/a	chr4:3011208-3011221
46	CTCF	chr4:3011360-3011510	GM12865	blood:	n/a	n/a
47	CTCF	chr4:3010976-3011523	HCT-116	colon:	n/a	chr4:3011208-3011221
48	CTCF	chr4:3011180-3011330	BE2_C	brain:	n/a	chr4:3011208-3011221
49	CTCF	chr4:3011180-3011330	HEK293	kidney:	n/a	chr4:3011208-3011221
50	CTCF	chr4:3011160-3011310	BJ	skin:	n/a	chr4:3011208-3011221

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3013267-3013317	HL-60	blood:	n/a
2	chr4:3013267-3013317	HRCEpiC	kidney:	n/a
3	chr4:3000970-3001020	SK-N-SH	brain:	n/a
4	chr4:3000970-3001020	AG09309	skin:	n/a
5	chr4:3013267-3013317	HEK293	kidney:	embryo
6	chr4:3000970-3001020	T-47D	breast:	n/a
7	chr4:3013267-3013317	PrEC	prostate:	n/a
8	chr4:3000970-3001020	BE2_C	brain:	n/a
9	chr4:3013267-3013317	HCF	heart:	n/a
10	chr4:3000970-3001020	HepG2	liver:	n/a
11	chr4:3000970-3001020	PANC-1	pancreas:	n/a
12	chr4:3013267-3013317	HCT-116	colon:	n/a
13	chr4:3000970-3001020	CMK	blood:	n/a
14	chr4:3000970-3001020	NB4	blood:	n/a
15	chr4:3013267-3013317	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:3000970-3001020	HCT-116	colon:	n/a
17	chr4:3013267-3013317	ovcar-3	ovarian:	n/a
18	chr4:3000970-3001020	SK-N-SH_RA	brain:	n/a
19	chr4:3000970-3001020	SK-N-MC	brain:	n/a
20	chr4:3013267-3013317	ECC-1	luminal epithelium:	n/a
21	chr4:3000970-3001020	ProgFib	skin:	n/a
22	chr4:3000970-3001020	HEK293	kidney:	embryo
23	chr4:3000970-3001020	MCF10A-Er-Src	breast:	n/a
24	chr4:3000970-3001020	SKMC	muscle:	n/a
25	chr4:3000970-3001020	Hela-S3	cervix:	n/a
26	chr4:3013267-3013317	HNPCEpiC	eye:	n/a
27	chr4:3013267-3013317	IMR90	lung:	fetal
28	chr4:3013267-3013317	HRE	kidney:	n/a
29	chr4:3000970-3001020	AoSMC	blood vessel:	n/a
30	chr4:3000970-3001020	NT2-D1	testis:	n/a
31	chr4:3013267-3013317	NHDF-neo	bronchial:	n/a
32	chr4:3000970-3001020	HRPEpiC	eye:	n/a
33	chr4:3013267-3013317	HMEC	breast:	n/a
34	chr4:3013267-3013317	HIPEpiC	eye:	n/a
35	chr4:3000970-3001020	GM19239	blood:	n/a
36	chr4:3013267-3013317	SK-N-SH_RA	brain:	n/a
37	chr4:3000970-3001020	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:3013267-3013317	AG10803	skin:	n/a
39	chr4:3013267-3013317	LNCaP	prostate:	n/a
40	chr4:3013267-3013317	RPTEC	kidney:	n/a
41	chr4:3013267-3013317	MCF10A-Er-Src	breast:	n/a
42	chr4:3013267-3013317	NHBE	bronchial:	n/a
43	chr4:3000970-3001020	HNPCEpiC	eye:	n/a
44	chr4:3000970-3001020	HRE	kidney:	n/a
45	chr4:3000970-3001020	SAEC	small airway:	n/a
46	chr4:3013267-3013317	BJ	skin:	n/a
47	chr4:3000970-3001020	ovcar-3	ovarian:	n/a
48	chr4:3000970-3001020	H1-hESC	embryonic stem cell:	embryo
49	chr4:3013267-3013317	BE2_C	brain:	n/a
50	chr4:3013267-3013317	Caco-2	colon:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3014192..3017069-chr4:3021177..3023631,3	MCF-7	breast:
2	chr4:2963576..2965499-chr4:3012277..3014401,2	MCF-7	breast:
3	chr4:2982899..2985066-chr4:2988883..2990462,2	K562	blood:
4	chr4:2999092..3001620-chr4:3007544..3009906,2	K562	blood:
5	chr4:3005911..3008634-chr4:3009040..3011170,2	K562	blood:
6	chr4:2993023..2995756-chr4:3021120..3023336,2	K562	blood:
7	chr4:3009009..3010811-chr4:3023139..3026121,2	MCF-7	breast:
8	chr4:3005911..3008634-chr4:3009040..3011170,2	K562	blood:
9	chr4:2999092..3001620-chr4:3007544..3009906,2	K562	blood:
10	chr4:2968827..2971800-chr4:2992655..2994613,2	K562	blood:
11	chr4:2982899..2985113-chr4:2988868..2990462,2	K562	blood:
12	chr4:2985299..2988258-chr4:2989920..2992919,2	MCF-7	breast:
13	chr4:2976299..2978558-chr4:2988951..2991027,2	K562	blood:
14	chr4:3013109..3014108-chr4:3038245..3039224,2	MCF-7	breast:
15	chr4:2979113..2981716-chr4:2982271..2984817,3	K562	blood:
16	chr4:2979100..2980940-chr4:2982118..2984600,2	K562	blood:
17	chr4:2982899..2985066-chr4:2988883..2990462,2	K562	blood:
18	chr4:2985299..2988258-chr4:2989920..2992919,2	MCF-7	breast:
19	chr4:2982899..2985113-chr4:2988868..2990462,2	K562	blood:
20	chr4:3018174..3020702-chr4:3033149..3035884,2	MCF-7	breast:
21	chr4:2938205..2940461-chr4:3011705..3013436,2	MCF-7	breast:
22	chr4:2993023..2995756-chr4:3021120..3023336,2	K562	blood:
23	chr4:3014192..3017069-chr4:3021177..3023631,3	MCF-7	breast:
24	chr4:2978330..2980789-chr4:2984155..2986237,2	MCF-7	breast:

No data

Variant related genes	Relation type
GRK4	TF binding region
GRK4	CpG island
ENSG00000087269	chromatin interactions
ENSG00000125388	chromatin interactions
ENSG00000249673	chromatin interactions

Extended variants
information (count: 1677 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1677 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561040177	chr4:2982253-2982254	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs542327309	chr4:2982255-2982256	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs559313455	chr4:2982287-2982288	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs34626132	chr4:2982291-2982292	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs12645113	chr4:2982318-2982319	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs551654544	chr4:2982343-2982344	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs564831567	chr4:2982357-2982358	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs186407613	chr4:2982432-2982433	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550341911	chr4:2982444-2982445	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3021136	chr4:2982459-2982460	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs140799427	chr4:2982526-2982527	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536766316	chr4:2982527-2982528	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528635499	chr4:2982591-2982592	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546739235	chr4:2982605-2982606	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs566863773	chr4:2982617-2982618	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs112825243	chr4:2982623-2982624	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs114202729	chr4:2982656-2982657	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs373943034	chr4:2982745-2982746	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs4690068	chr4:2982768-2982769	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs538469064	chr4:2982787-2982788	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs555220495	chr4:2982820-2982821	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112405407	chr4:2982826-2982827	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77504251	chr4:2982906-2982907	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2105380	chr4:2982929-2982930	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs139394138	chr4:2982932-2982933	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113510686	chr4:2982949-2982950	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77164310	chr4:2982977-2982978	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111361056	chr4:2982978-2982979	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564866186	chr4:2983025-2983026	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112892393	chr4:2983127-2983128	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35448179	chr4:2983144-2983145	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189202072	chr4:2983150-2983151	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534417278	chr4:2983214-2983215	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34382487	chr4:2983247-2983248	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368829085	chr4:2983255-2983256	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181529905	chr4:2983257-2983258	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560758534	chr4:2983294-2983295	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529805652	chr4:2983297-2983298	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547119513	chr4:2983391-2983392	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566841682	chr4:2983397-2983398	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373531587	chr4:2983411-2983412	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552583510	chr4:2983445-2983446	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569246374	chr4:2983452-2983453	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538551205	chr4:2983478-2983479	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540449647	chr4:2983554-2983555	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146778088	chr4:2983556-2983557	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185982129	chr4:2983576-2983577	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139518262	chr4:2983586-2983587	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572831457	chr4:2983604-2983605	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545062845	chr4:2983613-2983614	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2966600-2982200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr4:2966800-2982200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:2967200-2983800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:2967400-2982600	Weak transcription	Pancreas	Pancrea
5	chr4:2967400-2983000	Weak transcription	Fetal Lung	lung
6	chr4:2967400-2983600	Weak transcription	Gastric	stomach
7	chr4:2979400-2982600	Weak transcription	Brain Anterior Caudate	brain
8	chr4:2979600-2982400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:2979600-3025000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr4:2979800-2983600	Weak transcription	HSMMtube	muscle
11	chr4:2980200-2982400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:2980200-2982400	Weak transcription	Brain Substantia Nigra	brain
13	chr4:2980400-2984000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:2980600-2983400	Weak transcription	Right Ventricle	heart
15	chr4:2980600-2992000	Weak transcription	Fetal Heart	heart
16	chr4:2981800-2982200	Weak transcription	Fetal Brain Female	brain
17	chr4:2981800-2983400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:2981800-2983400	ZNF genes & repeats	Fetal Stomach	stomach
19	chr4:2981800-2984000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:2981800-2984200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr4:2982000-2982400	Weak transcription	Brain Hippocampus Middle	brain
22	chr4:2982000-2983400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
23	chr4:2982000-2984000	ZNF genes & repeats	Brain Germinal Matrix	brain
24	chr4:2982200-2982600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr4:2982400-2982800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:2982400-2984200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:2982600-2982800	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:2982600-2982800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:2982600-2982800	ZNF genes & repeats	Pancreas	Pancrea
30	chr4:2982600-2983600	ZNF genes & repeats	Fetal Brain Female	brain
31	chr4:2982800-2983000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr4:2983000-2983200	ZNF genes & repeats	Brain Anterior Caudate	brain
33	chr4:2983000-2983200	ZNF genes & repeats	Brain Hippocampus Middle	brain
34	chr4:2983000-2983400	ZNF genes & repeats	Fetal Lung	lung
35	chr4:2983200-2997000	Weak transcription	Brain Hippocampus Middle	brain
36	chr4:2983400-2984000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr4:2983400-2984000	Enhancers	Right Ventricle	heart
38	chr4:2983400-2988800	Weak transcription	Fetal Lung	lung
39	chr4:2983600-2984200	Enhancers	Gastric	stomach
40	chr4:2983600-3032000	Weak transcription	Fetal Brain Female	brain
41	chr4:2983800-2984400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:2984000-2985400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:2984200-2991800	Weak transcription	Gastric	stomach
44	chr4:2984400-2984800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:2984600-2985000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:2984800-2985800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:2985200-2985400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr4:2985800-2989400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:2986800-2991000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr4:2988800-2989400	ZNF genes & repeats	Fetal Lung	lung

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