Variant report

Variant	nsv548297
Chromosome Location	chr1:179371973-179477921
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:396)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:396 , 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	chr1:179417315-179418149	K562	blood:	n/a	n/a
2	ATF1	chr1:179372366-179372548	K562	blood:	n/a	n/a
3	BACH1	chr1:179417282-179417546	K562	blood:	n/a	n/a
4	BHLHE40	chr1:179416680-179416751	K562	blood:	n/a	n/a
5	BHLHE40	chr1:179417644-179417794	K562	blood:	n/a	chr1:179417771-179417787
6	CBX3	chr1:179445580-179446074	HCT-116	colon:	n/a	n/a
7	CBX3	chr1:179445633-179446049	K562	blood:	n/a	n/a
8	CBX3	chr1:179445638-179446037	K562	blood:	n/a	n/a
9	CBX3	chr1:179445664-179446046	HCT-116	colon:	n/a	n/a
10	CBX3	chr1:179393797-179394101	HCT-116	colon:	n/a	n/a
11	CCNT2	chr1:179417639-179417843	K562	blood:	n/a	n/a
12	CEBPB	chr1:179471785-179471955	K562	blood:	n/a	n/a
13	CEBPB	chr1:179468682-179468724	K562	blood:	n/a	n/a
14	CEBPB	chr1:179471685-179471978	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:179471780-179471966	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:179410223-179410324	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:179471742-179471926	A549	lung:	n/a	n/a
18	CEBPB	chr1:179417959-179418279	K562	blood:	n/a	n/a
19	CEBPB	chr1:179403206-179403320	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:179413229-179413547	K562	blood:	n/a	n/a
21	CEBPB	chr1:179451118-179451130	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:179468606-179468861	A549	lung:	n/a	n/a
23	CEBPB	chr1:179471773-179471946	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:179417922-179418292	K562	blood:	n/a	n/a
25	CHD2	chr1:179416662-179416860	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:179416723-179416877	GM19239	blood:	n/a	n/a
27	CTCF	chr1:179416720-179416870	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr1:179416720-179416870	GM12872	blood:	n/a	n/a
29	CTCF	chr1:179475478-179475592	HepG2	liver:	n/a	n/a
30	CTCF	chr1:179416720-179416870	NHLF	lung:	n/a	n/a
31	CTCF	chr1:179416640-179416790	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr1:179416600-179416750	NHEK	skin:	n/a	n/a
33	CTCF	chr1:179416640-179416790	HFF	foreskin:	n/a	n/a
34	CTCF	chr1:179416760-179416910	BJ	skin:	n/a	n/a
35	CTCF	chr1:179416720-179416870	K562	blood:	n/a	n/a
36	CTCF	chr1:179416760-179416910	GM12869	blood:	n/a	n/a
37	CTCF	chr1:179416680-179416830	GM12878	blood:	n/a	n/a
38	CTCF	chr1:179416780-179416930	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr1:179410812-179410862	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:179410788-179410847	HepG2	liver:	n/a	n/a
41	CTCF	chr1:179461286-179461332	LNCaP	prostate:	n/a	n/a
42	CTCF	chr1:179410700-179410966	K562	blood:	n/a	n/a
43	CTCF	chr1:179427249-179427289	GM13976	blood:	n/a	n/a
44	CTCF	chr1:179416720-179416870	GM12865	blood:	n/a	n/a
45	CTCF	chr1:179416720-179416870	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr1:179416700-179416850	GM12874	blood:	n/a	n/a
47	CTCF	chr1:179416730-179416873	GM19240	blood:	n/a	n/a
48	CTCF	chr1:179416760-179416910	GM12865	blood:	n/a	n/a
49	CTCF	chr1:179416700-179416850	GM12873	blood:	n/a	n/a
50	CTCF	chr1:179416780-179416930	AG09319	gingival:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179459849-179459899	K562	blood:	n/a
2	chr1:179459849-179459899	AG04449	skin:	fetal
3	chr1:179459849-179459899	NT2-D1	testis:	n/a
4	chr1:179459849-179459899	HAEpiC	amniotic membrane:	n/a
5	chr1:179459849-179459899	SK-N-SH	brain:	n/a
6	chr1:179459849-179459899	GM12878	blood:	n/a
7	chr1:179459849-179459899	T-47D	breast:	n/a
8	chr1:179459849-179459899	Jurkat	blood:	n/a
9	chr1:179459849-179459899	SAEC	small airway:	n/a
10	chr1:179459849-179459899	A549	lung:	n/a
11	chr1:179459849-179459899	SKMC	muscle:	n/a
12	chr1:179459849-179459899	HNPCEpiC	eye:	n/a
13	chr1:179459849-179459899	HCF	heart:	n/a
14	chr1:179459849-179459899	BJ	skin:	n/a
15	chr1:179459849-179459899	H1-hESC	embryonic stem cell:	embryo
16	chr1:179459849-179459899	HCT-116	colon:	n/a
17	chr1:179459849-179459899	ECC-1	luminal epithelium:	n/a
18	chr1:179459849-179459899	PANC-1	pancreas:	n/a
19	chr1:179459849-179459899	ovcar-3	ovarian:	n/a
20	chr1:179459849-179459899	HRE	kidney:	n/a
21	chr1:179459849-179459899	HUVEC	blood vessel:	n/a
22	chr1:179459849-179459899	BE2_C	brain:	n/a
23	chr1:179459849-179459899	CMK	blood:	n/a
24	chr1:179459849-179459899	U87	brain:	n/a
25	chr1:179459849-179459899	HCM	heart:	n/a
26	chr1:179459849-179459899	AoSMC	blood vessel:	n/a
27	chr1:179459849-179459899	Caco-2	colon:	n/a
28	chr1:179459849-179459899	AG09309	skin:	n/a
29	chr1:179459849-179459899	HRPEpiC	eye:	n/a
30	chr1:179459849-179459899	HCPEpiC	choroid plexus:	n/a
31	chr1:179459849-179459899	HepG2	liver:	n/a
32	chr1:179459849-179459899	AG04450	lung:	fetal
33	chr1:179459849-179459899	HRCEpiC	kidney:	n/a
34	chr1:179459849-179459899	GM19239	blood:	n/a
35	chr1:179459849-179459899	HMEC	breast:	n/a
36	chr1:179459849-179459899	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:179459849-179459899	GM12892	blood:	n/a
38	chr1:179459849-179459899	MCF10A-Er-Src	breast:	n/a
39	chr1:179459849-179459899	LNCaP	prostate:	n/a
40	chr1:179459849-179459899	GM12891	blood:	n/a
41	chr1:179459849-179459899	Hepatocyte	liver:	n/a
42	chr1:179459849-179459899	HL-60	blood:	n/a
43	chr1:179459849-179459899	MCF-7	breast:	n/a
44	chr1:179459849-179459899	AG10803	skin:	n/a
45	chr1:179459849-179459899	HIPEpiC	eye:	n/a
46	chr1:179459849-179459899	NB4	blood:	n/a
47	chr1:179459849-179459899	HEK293	kidney:	embryo
48	chr1:179459849-179459899	NHBE	bronchial:	n/a
49	chr1:179459849-179459899	NH-A	brain:	n/a
50	chr1:179459849-179459899	RPTEC	kidney:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179465791..179468521-chr1:179470887..179473606,2	MCF-7	breast:
2	chr1:179341117..179341930-chr1:179397158..179397756,2	MCF-7	breast:
3	chr1:179414237..179416318-chr1:179560640..179562488,2	MCF-7	breast:
4	chr1:179450571..179452564-chr1:179459735..179462060,2	K562	blood:
5	chr1:179420955..179423707-chr1:179426882..179428656,2	K562	blood:
6	chr1:179452715..179454955-chr1:179456900..179459797,2	MCF-7	breast:
7	chr1:179477575..179481033-chr1:179483963..179487085,3	K562	blood:
8	chr1:179464371..179466688-chr1:179474524..179476785,2	MCF-7	breast:
9	chr1:179465791..179468521-chr1:179470887..179473606,2	MCF-7	breast:
10	chr1:179408823..179410527-chr1:179414662..179417302,2	K562	blood:
11	chr1:179445378..179447823-chr1:179449930..179453030,3	MCF-7	breast:
12	chr1:179408823..179410527-chr1:179414662..179417302,2	K562	blood:
13	chr1:179445378..179447823-chr1:179449930..179453030,3	MCF-7	breast:
14	chr1:179464371..179466688-chr1:179474524..179476785,2	MCF-7	breast:
15	chr1:179420955..179423707-chr1:179426882..179428656,2	K562	blood:
16	chr1:179366133..179368260-chr1:179371106..179373571,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TDRD5-3	chr1:179473391-179473496	NONHSAT007863
2	lnc-TDRD5-3	chr1:179472147-179472264	NONHSAT007863
3	lnc-SOAT1-3	chr1:179411096-179411192	NONHSAT007860
4	lnc-SOAT1-3	chr1:179417648-179417967	NONHSAT007859
5	lnc-SOAT1-3	chr1:179410243-179410334	NONHSAT007859
6	lnc-SOAT1-3	chr1:179417648-179417966	NONHSAT007860
7	lnc-NPHS2-4	chr1:179426230-179426567	NONHSAT007862
8	lnc-NPHS2-5	chr1:179416713-179417575	NONHSAT007861
9	lnc-TDRD5-3	chr1:179474329-179474363	NONHSAT007863
10	lnc-SOAT1-3	chr1:179411096-179411225	NONHSAT007859
11	lnc-SOAT1-3	chr1:179411469-179411593	NONHSAT007860
12	lnc-NPHS2-4	chr1:179426715-179426908	NONHSAT007862

No data

Variant related genes	Relation type
HNRNPA1P54	TF binding region
MEF2AP1	TF binding region
ENSG00000269064	TF binding region
AXDND1	TF binding region
HNRNPA1P54	CpG island
MEF2AP1	CpG island
ENSG00000269064	CpG island
AXDND1	CpG island
ENSG00000162779	chromatin interactions
ENSG00000269064	chromatin interactions
ENSG00000162782	chromatin interactions
SATB2	miRNA target sites
PLS3	miRNA target sites

Extended variants
information (count: 1378 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1378 , 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	rs11586744	chr1:179386253-179386254	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs201985331	chr1:179386296-179386297	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs147145791	chr1:179386323-179386324	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs141201555	chr1:179386326-179386327	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs528341102	chr1:179386327-179386328	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs548184820	chr1:179386329-179386330	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs374825528	chr1:179386337-179386338	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs398103407	chr1:179386339-179386340	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs574003743	chr1:179386378-179386379	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs542962249	chr1:179386399-179386400	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs140261140	chr1:179386411-179386412	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs144338390	chr1:179386464-179386465	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs551453779	chr1:179386525-179386526	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs572133032	chr1:179386542-179386543	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs540811239	chr1:179386543-179386544	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs565402838	chr1:179386556-179386557	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs145829309	chr1:179386564-179386565	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs547624436	chr1:179386586-179386587	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs567510855	chr1:179386619-179386620	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs191663175	chr1:179386625-179386626	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs550124385	chr1:179386640-179386641	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs569833694	chr1:179386647-179386648	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs538641661	chr1:179386652-179386653	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs558238701	chr1:179386707-179386708	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs547068763	chr1:179386864-179386865	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs572109385	chr1:179386865-179386866	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs534374158	chr1:179386874-179386875	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs554241210	chr1:179386889-179386890	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs573924992	chr1:179386893-179386894	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs539984078	chr1:179386907-179386908	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs148888569	chr1:179386932-179386933	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs113262413	chr1:179386956-179386957	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs576635360	chr1:179387015-179387016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12758415	chr1:179387050-179387051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs373482518	chr1:179387084-179387085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535992963	chr1:179387089-179387090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142610714	chr1:179387095-179387096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12754425	chr1:179387109-179387110	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs113809356	chr1:179387140-179387141	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
40	rs561344100	chr1:179387167-179387168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200204317	chr1:179387277-179387278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549673935	chr1:179387379-179387380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557699891	chr1:179387405-179387406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569954827	chr1:179387406-179387407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532259006	chr1:179387437-179387438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111987712	chr1:179387545-179387546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565579535	chr1:179387649-179387650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377394165	chr1:179387681-179387682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534298369	chr1:179387698-179387699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201354292	chr1:179387726-179387727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	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
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179386200-179387000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:179387000-179389000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:179389000-179390400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:179391600-179394800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:179393600-179394600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr1:179394600-179394800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:179396800-179397400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:179398400-179398800	Enhancers	Duodenum Mucosa	Duodenum
9	chr1:179405200-179413000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:179405600-179406000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:179408800-179411400	Enhancers	Fetal Intestine Small	intestine
12	chr1:179409600-179411000	Enhancers	HepG2	liver
13	chr1:179411800-179412800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:179412800-179413600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:179414000-179414200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:179416800-179417400	Enhancers	K562	blood
17	chr1:179417400-179417600	Flanking Active TSS	K562	blood
18	chr1:179417600-179418000	Active TSS	K562	blood
19	chr1:179418000-179418600	Enhancers	K562	blood
20	chr1:179447000-179448000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:179447000-179448600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:179448600-179449400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:179453600-179454000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:179454000-179454400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:179476400-179476800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:179476600-179477800	Enhancers	Stomach Mucosa	stomach
27	chr1:179476800-179478200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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