Variant report

Variant	nsv870442
Chromosome Location	chr1:242105882-242136576
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	ARID3A	chr1:242135954-242136215	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:242107314-242107371	K562	blood:	n/a	n/a
3	ATF1	chr1:242128209-242128497	K562	blood:	n/a	n/a
4	ATF1	chr1:242130694-242130726	K562	blood:	n/a	n/a
5	ATF3	chr1:242136065-242136245	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr1:242136045-242136302	K562	blood:	n/a	n/a
7	BHLHE40	chr1:242106090-242106337	K562	blood:	n/a	chr1:242106181-242106190 chr1:242106180-242106189 chr1:242106180-242106189
8	BHLHE40	chr1:242111843-242111974	K562	blood:	n/a	n/a
9	BHLHE40	chr1:242121224-242121872	K562	blood:	n/a	n/a
10	CBX3	chr1:242121536-242121885	K562	blood:	n/a	n/a
11	CEBPB	chr1:242135874-242136183	IMR90	lung:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
12	CEBPB	chr1:242120460-242120534	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:242108042-242108506	A549	lung:	n/a	n/a
14	CEBPB	chr1:242135926-242136336	H1-hESC	embryonic stem cell:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
15	CEBPB	chr1:242127958-242128206	H1-hESC	embryonic stem cell:	n/a	chr1:242128050-242128061
16	CEBPB	chr1:242127931-242128152	K562	blood:	n/a	chr1:242128050-242128061
17	CEBPB	chr1:242108052-242108469	K562	blood:	n/a	n/a
18	CEBPB	chr1:242135784-242136341	K562	blood:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
19	CEBPB	chr1:242108167-242108513	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:242108114-242108469	MCF-7	breast:	n/a	n/a
21	CEBPB	chr1:242127849-242128342	K562	blood:	n/a	chr1:242128050-242128061
22	CEBPB	chr1:242135790-242136340	HepG2	liver:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
23	CEBPB	chr1:242135831-242136336	A549	lung:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
24	CEBPB	chr1:242127883-242128178	K562	blood:	n/a	chr1:242128050-242128061
25	CEBPB	chr1:242127899-242128239	MCF-7	breast:	n/a	chr1:242128050-242128061
26	CEBPB	chr1:242108156-242108512	K562	blood:	n/a	n/a
27	CEBPB	chr1:242131600-242131768	A549	lung:	n/a	n/a
28	CEBPB	chr1:242108077-242108499	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:242135942-242136282	Hela-S3	cervix:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
30	CEBPB	chr1:242125193-242125314	K562	blood:	n/a	n/a
31	CEBPB	chr1:242105798-242106007	A549	lung:	n/a	n/a
32	CEBPB	chr1:242127950-242128236	HepG2	liver:	n/a	chr1:242128050-242128061
33	CEBPB	chr1:242105799-242106097	K562	blood:	n/a	n/a
34	CEBPB	chr1:242127874-242128487	Hela-S3	cervix:	n/a	chr1:242128050-242128061
35	CEBPB	chr1:242127958-242128195	A549	lung:	n/a	chr1:242128050-242128061
36	CEBPB	chr1:242108205-242108449	A549	lung:	n/a	n/a
37	CEBPB	chr1:242135805-242136343	HepG2	liver:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
38	CEBPB	chr1:242135979-242136319	K562	blood:	n/a	chr1:242136167-242136178
39	CHD2	chr1:242121333-242121484	K562	blood:	n/a	n/a
40	CTCF	chr1:242121173-242121385	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:242121199-242121360	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:242121595-242121848	K562	blood:	n/a	n/a
43	CTCF	chr1:242121620-242121770	HVMF	connective:	n/a	n/a
44	CTCF	chr1:242121200-242121350	HEK293	kidney:	n/a	n/a
45	CTCF	chr1:242121279-242121318	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr1:242121135-242121935	K562	blood:	n/a	n/a
47	CTCF	chr1:242121252-242121294	A549	lung:	n/a	n/a
48	CTCF	chr1:242121213-242121332	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:242121481-242121901	K562	blood:	n/a	n/a
50	CTCF	chr1:242121620-242121770	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242122063-242122113	NB4	blood:	n/a
2	chr1:242122063-242122113	IMR90	lung:	fetal
3	chr1:242121230-242121280	AG09319	gingival:	n/a
4	chr1:242120907-242120957	HMEC	breast:	n/a
5	chr1:242120907-242120957	IMR90	lung:	fetal
6	chr1:242122063-242122113	CMK	blood:	n/a
7	chr1:242120638-242120688	Caco-2	colon:	n/a
8	chr1:242120638-242120688	BJ	skin:	n/a
9	chr1:242121526-242121576	NHDF-neo	bronchial:	n/a
10	chr1:242120907-242120957	CMK	blood:	n/a
11	chr1:242121526-242121576	HRCEpiC	kidney:	n/a
12	chr1:242121526-242121576	GM06990	blood:	n/a
13	chr1:242120907-242120957	AoSMC	blood vessel:	n/a
14	chr1:242120907-242120957	SKMC	muscle:	n/a
15	chr1:242121526-242121576	AG09319	gingival:	n/a
16	chr1:242121526-242121576	SK-N-SH_RA	brain:	n/a
17	chr1:242121526-242121576	NHBE	bronchial:	n/a
18	chr1:242121526-242121576	HCT-116	colon:	n/a
19	chr1:242120907-242120957	Jurkat	blood:	n/a
20	chr1:242121526-242121576	ProgFib	skin:	n/a
21	chr1:242120907-242120957	HRPEpiC	eye:	n/a
22	chr1:242122063-242122113	HAEpiC	amniotic membrane:	n/a
23	chr1:242120907-242120957	AG04449	skin:	fetal
24	chr1:242121526-242121576	HepG2	liver:	n/a
25	chr1:242120907-242120957	HepG2	liver:	n/a
26	chr1:242122063-242122113	Hepatocyte	liver:	n/a
27	chr1:242122063-242122113	AG09309	skin:	n/a
28	chr1:242120638-242120688	HUVEC	blood vessel:	n/a
29	chr1:242121230-242121280	HUVEC	blood vessel:	n/a
30	chr1:242121230-242121280	HepG2	liver:	n/a
31	chr1:242121827-242121877	PANC-1	pancreas:	n/a
32	chr1:242120907-242120957	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:242121827-242121877	HMEC	breast:	n/a
34	chr1:242120638-242120688	HNPCEpiC	eye:	n/a
35	chr1:242121230-242121280	MCF10A-Er-Src	breast:	n/a
36	chr1:242121526-242121576	IMR90	lung:	fetal
37	chr1:242121827-242121877	HCPEpiC	choroid plexus:	n/a
38	chr1:242120907-242120957	K562	blood:	n/a
39	chr1:242120638-242120688	HCM	heart:	n/a
40	chr1:242120907-242120957	SAEC	small airway:	n/a
41	chr1:242120638-242120688	ProgFib	skin:	n/a
42	chr1:242120907-242120957	ECC-1	luminal epithelium:	n/a
43	chr1:242120907-242120957	PANC-1	pancreas:	n/a
44	chr1:242122063-242122113	MCF10A-Er-Src	breast:	n/a
45	chr1:242120638-242120688	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:242120638-242120688	HIPEpiC	eye:	n/a
47	chr1:242121827-242121877	IMR90	lung:	fetal
48	chr1:242120907-242120957	HEEpiC	esophagus:	n/a
49	chr1:242120907-242120957	Hepatocyte	liver:	n/a
50	chr1:242121230-242121280	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:242121060..242121703-chr1:242148791..242149743,4	MCF-7	breast:
2	chr1:242096785..242098721-chr1:242103500..242105954,2	K562	blood:
3	chr1:242101934..242104578-chr1:242110497..242113039,2	K562	blood:
4	chr1:242102983..242105016-chr1:242106501..242108855,2	MCF-7	breast:
5	chr1:242130029..242131689-chr1:242138065..242140950,2	K562	blood:
6	chr1:242103745..242105916-chr1:242116702..242119562,2	K562	blood:
7	chr1:242120814..242121654-chr1:242161517..242162480,3	MCF-7	breast:
8	chr1:242103745..242105916-chr1:242116702..242119562,2	K562	blood:

Variant related genes	Relation type
BECN1P1	TF binding region
BECN1P1	CpG island
ENSG00000197769	chromatin interactions

Extended variants
information (count: 1393 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1393 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181600041	chr1:242105911-242105912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115284529	chr1:242105922-242105923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145873536	chr1:242106030-242106031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527484884	chr1:242106055-242106056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186675927	chr1:242106056-242106057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34516384	chr1:242106084-242106085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554100449	chr1:242106085-242106086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs61081373	chr1:242106096-242106097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564282890	chr1:242106120-242106121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192033782	chr1:242106140-242106141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549792767	chr1:242106143-242106144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148999716	chr1:242106176-242106177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529529768	chr1:242106184-242106185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549662820	chr1:242106217-242106218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566137132	chr1:242106230-242106231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs11581005	chr1:242106296-242106297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs549927525	chr1:242106297-242106298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570587163	chr1:242106317-242106318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539561089	chr1:242106366-242106367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569341175	chr1:242106400-242106401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536432580	chr1:242106433-242106434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114208786	chr1:242106438-242106439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576115786	chr1:242106441-242106442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11586627	chr1:242106442-242106443	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555681670	chr1:242106466-242106467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573176125	chr1:242106497-242106498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111424984	chr1:242106503-242106504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541254972	chr1:242106556-242106557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183499600	chr1:242106560-242106561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370207026	chr1:242106636-242106637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533227262	chr1:242106683-242106684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61826022	chr1:242106713-242106714	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs188946216	chr1:242106738-242106739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529333002	chr1:242106741-242106742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs137861609	chr1:242106756-242106757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566395899	chr1:242106758-242106759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376494839	chr1:242106759-242106760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551974742	chr1:242106766-242106767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142341895	chr1:242106773-242106774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539500288	chr1:242106788-242106789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191052336	chr1:242106789-242106790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569548262	chr1:242106791-242106792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566936403	chr1:242106793-242106794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535474335	chr1:242106796-242106797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555359853	chr1:242106815-242106816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112358173	chr1:242106830-242106831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367672368	chr1:242106835-242106836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75071221	chr1:242106838-242106839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs386370225	chr1:242106839-242106840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71174872	chr1:242106849-242106850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	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
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	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
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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	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
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242103600-242106000	Weak transcription	NHDF-Ad	bronchial
2	chr1:242105600-242106600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:242105800-242106400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:242106000-242106400	Enhancers	NHDF-Ad	bronchial
5	chr1:242106400-242113600	Weak transcription	NHDF-Ad	bronchial
6	chr1:242106600-242110200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:242107400-242107600	Enhancers	A549	lung
8	chr1:242107400-242107600	Enhancers	HepG2	liver
9	chr1:242107400-242108200	Flanking Active TSS	K562	blood
10	chr1:242107600-242107800	Flanking Active TSS	HepG2	liver
11	chr1:242107600-242108000	Enhancers	Placenta	Placenta
12	chr1:242107600-242108000	Flanking Active TSS	A549	lung
13	chr1:242107600-242108000	Enhancers	Osteobl	bone
14	chr1:242107600-242108600	Active TSS	Hela-S3	cervix
15	chr1:242107600-242109000	Active TSS	Duodenum Mucosa	Duodenum
16	chr1:242107800-242108000	Flanking Bivalent TSS/Enh	HepG2	liver
17	chr1:242107800-242108400	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr1:242107800-242108400	Active TSS	Rectal Mucosa Donor 31	rectum
19	chr1:242107800-242108600	Active TSS	Ovary	ovary
20	chr1:242108000-242108200	Flanking Active TSS	Placenta	Placenta
21	chr1:242108000-242108400	Active TSS	Psoas Muscle	Psoas
22	chr1:242108000-242108600	Active TSS	Osteobl	bone
23	chr1:242108000-242108800	Active TSS	A549	lung
24	chr1:242108000-242109200	Bivalent/Poised TSS	HepG2	liver
25	chr1:242108200-242108400	Enhancers	Dnd41	blood
26	chr1:242108200-242108800	Active TSS	K562	blood
27	chr1:242108200-242109000	Active TSS	Placenta	Placenta
28	chr1:242108600-242109000	Enhancers	Hela-S3	cervix
29	chr1:242108800-242109000	Flanking Active TSS	K562	blood
30	chr1:242108800-242109200	Enhancers	A549	lung
31	chr1:242110000-242111000	Enhancers	Fetal Muscle Leg	muscle
32	chr1:242110200-242111200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:242110800-242111000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:242110800-242111000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:242111000-242113800	Weak transcription	Fetal Muscle Leg	muscle
36	chr1:242111200-242113000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:242111200-242113600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:242113000-242114800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:242113400-242114200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:242113400-242114200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:242113600-242113800	Flanking Active TSS	NHDF-Ad	bronchial
42	chr1:242113600-242114000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:242113800-242114000	Enhancers	Fetal Muscle Leg	muscle
44	chr1:242113800-242114000	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr1:242113800-242114000	Enhancers	NHDF-Ad	bronchial
46	chr1:242114000-242114200	Flanking Active TSS	NHDF-Ad	bronchial
47	chr1:242114000-242121200	Weak transcription	Fetal Muscle Leg	muscle
48	chr1:242121000-242121200	Weak transcription	Right Atrium	heart
49	chr1:242121200-242121400	ZNF genes & repeats	Right Atrium	heart
50	chr1:242121200-242121400	Flanking Bivalent TSS/Enh	K562	blood

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