Variant report

Variant	nsv159946
Chromosome Location	chr1:228755745-228757939
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr1:228756724-228756902	GM12878	blood:	n/a	chr1:228756756-228756769 chr1:228756760-228756769 chr1:228756837-228756850 chr1:228756750-228756763 chr1:228756749-228756762
2	BCL3	chr1:228757842-228758009	GM12878	blood:	n/a	n/a
3	BCL3	chr1:228757836-228758031	GM12878	blood:	n/a	n/a
4	CBX3	chr1:228755550-228756714	K562	blood:	n/a	n/a
5	CBX3	chr1:228755385-228756425	K562	blood:	n/a	n/a
6	CBX3	chr1:228756716-228760610	K562	blood:	n/a	n/a
7	CBX3	chr1:228756779-228759666	K562	blood:	n/a	n/a
8	CEBPB	chr1:228757034-228757365	K562	blood:	n/a	n/a
9	CEBPB	chr1:228757789-228758242	GM12878	blood:	n/a	n/a
10	CEBPB	chr1:228755466-228755997	GM12878	blood:	n/a	n/a
11	CEBPB	chr1:228756995-228757561	GM12878	blood:	n/a	n/a
12	CEBPD	chr1:228757823-228758348	K562	blood:	n/a	n/a
13	CEBPD	chr1:228756659-228756869	HepG2	liver:	n/a	n/a
14	CHD2	chr1:228756661-228756864	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr1:228756766-228756968	HepG2	liver:	n/a	n/a
16	CTCF	chr1:228756700-228756850	GM12869	blood:	n/a	n/a
17	CTCF	chr1:228756660-228756810	GM12865	blood:	n/a	n/a
18	CTCF	chr1:228755033-228756371	K562	blood:	n/a	chr1:228755652-228755661 chr1:228756232-228756245 chr1:228755649-228755662
19	CTCF	chr1:228756660-228756810	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr1:228756640-228756790	GM12875	blood:	n/a	n/a
21	CTCF	chr1:228755699-228756163	K562	blood:	n/a	n/a
22	CTCF	chr1:228757848-228758573	K562	blood:	n/a	chr1:228758435-228758448 chr1:228757867-228757876 chr1:228757864-228757877
23	CTCF	chr1:228755808-228756208	K562	blood:	n/a	n/a
24	CTCF	chr1:228756680-228756830	BE2_C	brain:	n/a	n/a
25	CTCF	chr1:228756660-228756810	GM12875	blood:	n/a	n/a
26	CTCF	chr1:228756640-228756790	GM12872	blood:	n/a	n/a
27	CTCF	chr1:228757269-228757476	K562	blood:	n/a	n/a
28	CTCF	chr1:228757122-228757587	K562	blood:	n/a	n/a
29	EBF1	chr1:228756714-228756901	GM12878	blood:	n/a	n/a
30	ELK1	chr1:228756615-228756806	Hela-S3	cervix:	n/a	n/a
31	EP300	chr1:228756748-228756900	GM12878	blood:	n/a	n/a
32	FOSL2	chr1:228756617-228756913	HepG2	liver:	n/a	n/a
33	FOXA2	chr1:228743895-228782766	A549	lung:	n/a	n/a
34	FOXM1	chr1:228756691-228757384	GM12878	blood:	n/a	n/a
35	FOXP2	chr1:228755607-228755874	PFSK-1	brain:	n/a	n/a
36	FOXP2	chr1:228757816-228758427	PFSK-1	brain:	n/a	n/a
37	FOXP2	chr1:228757454-228757695	PFSK-1	brain:	n/a	n/a
38	FOXP2	chr1:228757165-228757410	PFSK-1	brain:	n/a	n/a
39	FOXP2	chr1:228757084-228757643	SK-N-MC	brain:	n/a	n/a
40	FOXP2	chr1:228756312-228756532	PFSK-1	brain:	n/a	n/a
41	GTF2F1	chr1:228756772-228756809	Hela-S3	cervix:	n/a	n/a
42	HCFC1	chr1:228756677-228756907	Hela-S3	cervix:	n/a	n/a
43	HEY1	chr1:228755634-228755791	K562	blood:	n/a	n/a
44	HEY1	chr1:228756718-228756878	K562	blood:	n/a	chr1:228756754-228756769 chr1:228756751-228756766
45	HEY1	chr1:228756583-228756919	HepG2	liver:	n/a	chr1:228756662-228756677 chr1:228756751-228756766 chr1:228756754-228756769
46	IRF4	chr1:228756684-228756919	GM12878	blood:	n/a	n/a
47	JUND	chr1:228756630-228756893	HepG2	liver:	n/a	n/a
48	JUND	chr1:228744099-228759006	A549	lung:	n/a	chr1:228748791-228748805 chr1:228747728-228747737 chr1:228753273-228753287 chr1:228744309-228744323 chr1:228746550-228746564 chr1:228745487-228745496 chr1:228755514-228755528 chr1:228751032-228751046 chr1:228758886-228758895 chr1:228749969-228749978 chr1:228752210-228752219 chr1:228754451-228754460 chr1:228757729-228757743
49	JUND	chr1:228756948-228757554	A549	lung:	n/a	n/a
50	JUND	chr1:228755634-228755786	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228756714-228756764	SKMC	muscle:	n/a
2	chr1:228756711-228756761	MCF10A-Er-Src	breast:	n/a
3	chr1:228756711-228756761	HIPEpiC	eye:	n/a
4	chr1:228756711-228756761	SK-N-SH_RA	brain:	n/a
5	chr1:228756711-228756761	SAEC	small airway:	n/a
6	chr1:228756789-228756839	AoSMC	blood vessel:	n/a
7	chr1:228756714-228756764	K562	blood:	n/a
8	chr1:228756789-228756839	Hela-S3	cervix:	n/a
9	chr1:228756714-228756764	HRE	kidney:	n/a
10	chr1:228756789-228756839	NB4	blood:	n/a
11	chr1:228756789-228756839	HEK293	kidney:	embryo
12	chr1:228756714-228756764	HAEpiC	amniotic membrane:	n/a
13	chr1:228756714-228756764	HEK293	kidney:	embryo
14	chr1:228756789-228756839	RPTEC	kidney:	n/a
15	chr1:228756789-228756839	IMR90	lung:	fetal
16	chr1:228756711-228756761	U87	brain:	n/a
17	chr1:228756711-228756761	Jurkat	blood:	n/a
18	chr1:228756711-228756761	HEK293	kidney:	embryo
19	chr1:228756711-228756761	AG04449	skin:	fetal
20	chr1:228756789-228756839	BE2_C	brain:	n/a
21	chr1:228756711-228756761	HCT-116	colon:	n/a
22	chr1:228756789-228756839	AG04450	lung:	fetal
23	chr1:228756711-228756761	HAEpiC	amniotic membrane:	n/a
24	chr1:228756714-228756764	HRPEpiC	eye:	n/a
25	chr1:228756789-228756839	Hepatocyte	liver:	n/a
26	chr1:228756711-228756761	AG09309	skin:	n/a
27	chr1:228756789-228756839	H1-hESC	embryonic stem cell:	embryo
28	chr1:228756711-228756761	PrEC	prostate:	n/a
29	chr1:228756711-228756761	HCM	heart:	n/a
30	chr1:228756789-228756839	HepG2	liver:	n/a
31	chr1:228756711-228756761	GM12891	blood:	n/a
32	chr1:228756789-228756839	NHDF-neo	bronchial:	n/a
33	chr1:228756714-228756764	AG04450	lung:	fetal
34	chr1:228756789-228756839	PFSK-1	brain:	n/a
35	chr1:228756789-228756839	SK-N-SH_RA	brain:	n/a
36	chr1:228756789-228756839	GM06990	blood:	n/a
37	chr1:228756711-228756761	ECC-1	luminal epithelium:	n/a
38	chr1:228756789-228756839	HCM	heart:	n/a
39	chr1:228756711-228756761	NHBE	bronchial:	n/a
40	chr1:228756714-228756764	AoSMC	blood vessel:	n/a
41	chr1:228756714-228756764	AG09309	skin:	n/a
42	chr1:228756789-228756839	NT2-D1	testis:	n/a
43	chr1:228756711-228756761	Hepatocyte	liver:	n/a
44	chr1:228756714-228756764	GM12891	blood:	n/a
45	chr1:228756714-228756764	NB4	blood:	n/a
46	chr1:228756711-228756761	NB4	blood:	n/a
47	chr1:228756789-228756839	HEEpiC	esophagus:	n/a
48	chr1:228756711-228756761	ProgFib	skin:	n/a
49	chr1:228756711-228756761	AG10803	skin:	n/a
50	chr1:228756711-228756761	CMK	blood:	n/a

Variant related genes	Relation type
RNA5S5	TF binding region
RNA5S4	TF binding region
RNA5S6	TF binding region
RNA5S5	CpG island
RNA5S4	CpG island
RNA5S6	CpG island

Extended variants
information (count: 30 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61825674	chr1:228755813-228755814	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs61825675	chr1:228755824-228755825	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs565476855	chr1:228756114-228756115	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs567136545	chr1:228756374-228756375	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs372491454	chr1:228756381-228756382	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs534425433	chr1:228756449-228756450	Bivalent Enhancer Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs374229110	chr1:228756450-228756451	Bivalent Enhancer Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs377763726	chr1:228756472-228756473	Bivalent Enhancer Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs371121505	chr1:228756474-228756475	Bivalent Enhancer Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs371497698	chr1:228756577-228756578	Bivalent Enhancer Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs374914994	chr1:228756633-228756634	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs145056430	chr1:228756659-228756660	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs538626744	chr1:228756687-228756688	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs558730530	chr1:228756706-228756707	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs370326559	chr1:228756707-228756708	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs541259792	chr1:228756712-228756713	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
17	rs561105041	chr1:228756749-228756750	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
18	rs374092496	chr1:228756763-228756764	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
19	rs543656844	chr1:228756821-228756822	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
20	rs563543643	chr1:228756825-228756826	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
21	rs367987570	chr1:228756847-228756848	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs372142938	chr1:228756956-228756957	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs112069526	chr1:228756969-228756970	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs532411567	chr1:228757069-228757070	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs149825182	chr1:228757450-228757451	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
26	rs552151310	chr1:228757925-228757926	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs559449286	chr1:228757926-228757927	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs200234224	chr1:228757935-228757936	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs61825676	chr1:228757936-228757937	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs548519035	chr1:228757938-228757939	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228756400-228756600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
2	chr1:228756400-228756800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
3	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
4	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:228756600-228756800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:228756600-228756800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr1:228756600-228756800	Enhancers	Primary T cells fromperipheralblood	blood
8	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
9	chr1:228756600-228756800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
11	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
12	chr1:228756600-228756800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:228756600-228756800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
16	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
17	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:228756600-228756800	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
20	chr1:228756600-228756800	Bivalent Enhancer	Fetal Intestine Small	intestine
21	chr1:228756600-228756800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
23	chr1:228756600-228756800	Bivalent Enhancer	Fetal Thymus	thymus
24	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Gastric	stomach
25	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Left Ventricle	heart
26	chr1:228756600-228756800	Bivalent/Poised TSS	Small Intestine	intestine
27	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Spleen	Spleen
28	chr1:228756600-228757000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:228756600-228757000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:228756600-228757000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:228756600-228757000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:228756600-228757000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr1:228756600-228757000	Enhancers	Primary B cells from peripheral blood	blood
34	chr1:228756600-228757000	Active TSS	Primary T cells from cord blood	blood
35	chr1:228756600-228757000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr1:228756600-228757000	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr1:228756600-228757000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr1:228756600-228757000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr1:228756600-228757000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:228756600-228757000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr1:228756600-228757000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:228756600-228757000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr1:228756600-228757000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
44	chr1:228756600-228757000	Active TSS	Brain Angular Gyrus	brain
45	chr1:228756600-228757000	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr1:228756600-228757000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
47	chr1:228756600-228757000	ZNF genes & repeats	Esophagus	oesophagus
48	chr1:228756600-228757000	Bivalent Enhancer	Fetal Brain Male	brain
49	chr1:228756600-228757000	Flanking Bivalent TSS/Enh	Lung	lung
50	chr1:228756600-228757000	Flanking Bivalent TSS/Enh	Ovary	ovary

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