Variant report

Variant	nsv471192
Chromosome Location	chr22:27821656-27865344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:427)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:27858256-27858552	HepG2	liver:	n/a	n/a
2	BACH1	chr22:27851013-27851014	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr22:27849743-27849959	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr22:27858110-27858278	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr22:27827809-27828304	HCT-116	colon:	n/a	n/a
6	CEBPB	chr22:27830914-27831198	A549	lung:	n/a	chr22:27831045-27831058
7	CEBPB	chr22:27830987-27831224	H1-hESC	embryonic stem cell:	n/a	chr22:27831045-27831058
8	CEBPB	chr22:27858249-27858545	HepG2	liver:	n/a	n/a
9	CEBPB	chr22:27830948-27831171	K562	blood:	n/a	chr22:27831045-27831058
10	CEBPB	chr22:27830901-27831271	HepG2	liver:	n/a	chr22:27831045-27831058
11	CEBPB	chr22:27859025-27859065	HepG2	liver:	n/a	n/a
12	CEBPB	chr22:27830957-27831202	IMR90	lung:	n/a	chr22:27831045-27831058
13	CEBPB	chr22:27830885-27831288	A549	lung:	n/a	chr22:27831045-27831058
14	CHD2	chr22:27829717-27829847	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr22:27857413-27857767	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr22:27829937-27830117	MCF-7	breast:	n/a	n/a
17	CTCF	chr22:27829920-27830070	NHEK	skin:	n/a	n/a
18	CTCF	chr22:27834480-27834630	HBMEC	blood vessel:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
19	CTCF	chr22:27834540-27834690	BE2_C	brain:	n/a	chr22:27834586-27834599
20	CTCF	chr22:27829949-27830104	MCF-7	breast:	n/a	n/a
21	CTCF	chr22:27830010-27830079	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr22:27834480-27834630	SAEC	small airway:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
23	CTCF	chr22:27829990-27830077	Gliobla	brain:	n/a	n/a
24	CTCF	chr22:27864720-27864870	HEK293	kidney:	n/a	n/a
25	CTCF	chr22:27834540-27834690	BJ	skin:	n/a	chr22:27834586-27834599
26	CTCF	chr22:27834460-27834610	AG10803	skin:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
27	CTCF	chr22:27834572-27834657	Pancreas_OC	pancreas:	n/a	chr22:27834586-27834599
28	CTCF	chr22:27834520-27834670	HEEpiC	esophagus:	n/a	chr22:27834586-27834599
29	CTCF	chr22:27834500-27834650	NHDF-neo	bronchial:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
30	CTCF	chr22:27834580-27834730	HCM	heart:	n/a	chr22:27834586-27834599
31	CTCF	chr22:27834500-27834650	MCF-7	breast:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
32	CTCF	chr22:27833160-27833310	HRE	kidney:	n/a	n/a
33	CTCF	chr22:27834460-27834610	AG04449	skin:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
34	CTCF	chr22:27834540-27834690	SK-N-SH_RA	brain:	n/a	chr22:27834586-27834599
35	CTCF	chr22:27834140-27834290	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr22:27834480-27834630	AG04449	skin:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
37	CTCF	chr22:27834540-27834690	HCPEpiC	choroid plexus:	n/a	chr22:27834586-27834599
38	CTCF	chr22:27834460-27834610	HBMEC	blood vessel:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
39	CTCF	chr22:27834540-27834690	HRPEpiC	eye:	n/a	chr22:27834586-27834599
40	CTCF	chr22:27829840-27829990	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr22:27834520-27834670	HCPEpiC	choroid plexus:	n/a	chr22:27834586-27834599
42	CTCF	chr22:27829951-27830115	MCF-7	breast:	n/a	n/a
43	CTCF	chr22:27834240-27834390	BJ	skin:	n/a	n/a
44	CTCF	chr22:27852114-27852131	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr22:27853716-27853724	K562	blood:	n/a	n/a
46	CTCF	chr22:27834520-27834670	HAc	cerebellar:	n/a	chr22:27834586-27834599
47	CTCF	chr22:27834460-27834610	AoAF	blood vessel:	n/a	chr22:27834505-27834518 chr22:27834586-27834599
48	CTCF	chr22:27834520-27834670	AG09319	gingival:	n/a	chr22:27834586-27834599
49	CTCF	chr22:27834580-27834730	AG10803	skin:	n/a	chr22:27834586-27834599
50	CTCF	chr22:27865320-27865470	HA-sp	spinal cord:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:27834549-27834599	ECC-1	luminal epithelium:	n/a
2	chr22:27834439-27834489	HIPEpiC	eye:	n/a
3	chr22:27834629-27834679	Hela-S3	cervix:	n/a
4	chr22:27831818-27831868	HAEpiC	amniotic membrane:	n/a
5	chr22:27835596-27835646	U87	brain:	n/a
6	chr22:27835596-27835646	PFSK-1	brain:	n/a
7	chr22:27831818-27831868	HMEC	breast:	n/a
8	chr22:27831818-27831868	IMR90	lung:	fetal
9	chr22:27832684-27832734	Hepatocyte	liver:	n/a
10	chr22:27834549-27834599	NT2-D1	testis:	n/a
11	chr22:27838621-27838671	PFSK-1	brain:	n/a
12	chr22:27834629-27834679	Caco-2	colon:	n/a
13	chr22:27834439-27834489	NT2-D1	testis:	n/a
14	chr22:27834439-27834489	GM06990	blood:	n/a
15	chr22:27838621-27838671	GM12892	blood:	n/a
16	chr22:27835596-27835646	HAEpiC	amniotic membrane:	n/a
17	chr22:27834439-27834489	ProgFib	skin:	n/a
18	chr22:27831818-27831868	BJ	skin:	n/a
19	chr22:27832684-27832734	Caco-2	colon:	n/a
20	chr22:27834439-27834489	SAEC	small airway:	n/a
21	chr22:27834439-27834489	HUVEC	blood vessel:	n/a
22	chr22:27831818-27831868	AG09309	skin:	n/a
23	chr22:27838621-27838671	HepG2	liver:	n/a
24	chr22:27831818-27831868	GM06990	blood:	n/a
25	chr22:27838621-27838671	SK-N-MC	brain:	n/a
26	chr22:27831818-27831868	AG09319	gingival:	n/a
27	chr22:27834629-27834679	ECC-1	luminal epithelium:	n/a
28	chr22:27834439-27834489	Caco-2	colon:	n/a
29	chr22:27832684-27832734	HL-60	blood:	n/a
30	chr22:27835596-27835646	ECC-1	luminal epithelium:	n/a
31	chr22:27834439-27834489	HMEC	breast:	n/a
32	chr22:27838621-27838671	HCF	heart:	n/a
33	chr22:27832684-27832734	HCT-116	colon:	n/a
34	chr22:27835596-27835646	AoSMC	blood vessel:	n/a
35	chr22:27832684-27832734	HCM	heart:	n/a
36	chr22:27834439-27834489	HepG2	liver:	n/a
37	chr22:27835596-27835646	HCPEpiC	choroid plexus:	n/a
38	chr22:27834629-27834679	IMR90	lung:	fetal
39	chr22:27835596-27835646	GM06990	blood:	n/a
40	chr22:27834629-27834679	RPTEC	kidney:	n/a
41	chr22:27834549-27834599	AG09309	skin:	n/a
42	chr22:27838621-27838671	Hepatocyte	liver:	n/a
43	chr22:27834439-27834489	SK-N-SH	brain:	n/a
44	chr22:27834629-27834679	GM12878	blood:	n/a
45	chr22:27834439-27834489	MCF10A-Er-Src	breast:	n/a
46	chr22:27832684-27832734	SK-N-SH	brain:	n/a
47	chr22:27831818-27831868	ovcar-3	ovarian:	n/a
48	chr22:27831818-27831868	HCPEpiC	choroid plexus:	n/a
49	chr22:27831818-27831868	NB4	blood:	n/a
50	chr22:27832684-27832734	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:27832758..27834628-chr22:27836553..27838416,2	MCF-7	breast:
2	chr22:27777645..27778297-chr22:27830082..27831081,2	MCF-7	breast:
3	chr22:27857934..27860311-chr22:27860712..27862590,2	K562	blood:
4	chr22:27813673..27816169-chr22:27820833..27822951,2	MCF-7	breast:
5	chr22:27823489..27825867-chr22:27829603..27831710,2	K562	blood:
6	chr22:27857934..27860311-chr22:27860712..27862590,2	K562	blood:
7	chr22:27828309..27830905-chr22:27832011..27834515,2	K562	blood:
8	chr22:27824367..27826325-chr22:27829603..27833358,3	K562	blood:
9	chr22:27824367..27826325-chr22:27829603..27833358,3	K562	blood:
10	chr22:27823489..27825867-chr22:27829603..27831710,2	K562	blood:
11	chr22:27832758..27834628-chr22:27836553..27838416,2	MCF-7	breast:
12	chr22:27828309..27830905-chr22:27832011..27834515,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MN1-4	chr22:27853208-27853691	XLOC_014330
2	lnc-MN1-4	chr22:27855736-27856021	XLOC_014330

No data

Variant related genes	Relation type
ENSG00000227880	TF binding region
ENSG00000227880	CpG island
VCL	miRNA target sites
PHF12	miRNA target sites

Extended variants
information (count: 1932 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1932 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4822875	chr22:27821656-27821657	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374056146	chr22:27821657-27821658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377627394	chr22:27821663-27821664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529960444	chr22:27821712-27821713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549515673	chr22:27821813-27821814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190686562	chr22:27821881-27821882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551346427	chr22:27821906-27821907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550154344	chr22:27821907-27821908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149048736	chr22:27821971-27821972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539017847	chr22:27821987-27821988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553895736	chr22:27822008-27822009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11295518	chr22:27822013-27822014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs55691952	chr22:27822030-27822031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12627850	chr22:27822043-27822044	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs4822876	chr22:27822059-27822060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs554709578	chr22:27822129-27822130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576349540	chr22:27822140-27822141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543710870	chr22:27822201-27822202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4822877	chr22:27822231-27822232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576801097	chr22:27822269-27822270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143029194	chr22:27822277-27822278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559517831	chr22:27822294-27822295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182858220	chr22:27822318-27822319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76502143	chr22:27822321-27822322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs193233079	chr22:27822388-27822389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116718143	chr22:27822405-27822406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530843727	chr22:27822416-27822417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552230261	chr22:27822446-27822447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570724331	chr22:27822476-27822477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532431034	chr22:27822484-27822485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76565851	chr22:27822487-27822488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565853466	chr22:27822495-27822496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536317800	chr22:27822499-27822500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116512597	chr22:27822546-27822547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370240259	chr22:27822558-27822559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs5762138	chr22:27822562-27822563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs5752544	chr22:27822583-27822584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs114512135	chr22:27822596-27822597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540703860	chr22:27822641-27822642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552968897	chr22:27822670-27822671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34125528	chr22:27822671-27822672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574589839	chr22:27822729-27822730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183752240	chr22:27822747-27822748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs151155552	chr22:27822768-27822769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115480195	chr22:27822778-27822779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187935830	chr22:27822823-27822824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73880514	chr22:27822837-27822838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs5762139	chr22:27822897-27822898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs374365786	chr22:27822956-27822957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192181786	chr22:27822967-27822968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Cancer	21183584	CNVD
Breast cancer	17142309	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:27817400-27827000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr22:27817600-27829200	Weak transcription	Gastric	stomach
3	chr22:27820400-27825400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr22:27824600-27825000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr22:27825000-27826400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr22:27825200-27825400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr22:27825600-27825800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr22:27825600-27827200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr22:27825800-27827200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr22:27825800-27831800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr22:27826000-27826800	Enhancers	Fetal Kidney	kidney
12	chr22:27826000-27827000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr22:27826000-27827600	Bivalent Enhancer	Fetal Stomach	stomach
14	chr22:27826200-27827200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr22:27826200-27827400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr22:27826400-27826600	Bivalent Enhancer	Fetal Muscle Leg	muscle
17	chr22:27826400-27827200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr22:27826400-27827400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr22:27826400-27827400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr22:27826600-27827200	Enhancers	Fetal Lung	lung
21	chr22:27826800-27827600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr22:27827000-27827200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr22:27827000-27827200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr22:27827000-27827400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr22:27827200-27827400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr22:27827200-27827400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr22:27827200-27827400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr22:27827200-27831800	Weak transcription	Fetal Lung	lung
29	chr22:27827400-27828000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr22:27827400-27828400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr22:27827400-27828400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr22:27827400-27828400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr22:27827400-27829200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr22:27828000-27828400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr22:27828400-27829200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr22:27828400-27829200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr22:27828400-27829400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr22:27828400-27829400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr22:27828600-27830000	Enhancers	Fetal Intestine Small	intestine
40	chr22:27828800-27829800	Enhancers	Fetal Intestine Large	intestine
41	chr22:27829000-27830000	Enhancers	HepG2	liver
42	chr22:27829000-27831400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr22:27829200-27829600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr22:27829200-27829600	Enhancers	Adipose Nuclei	Adipose
45	chr22:27829200-27829800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr22:27829200-27829800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr22:27829200-27829800	Enhancers	Duodenum Mucosa	Duodenum
48	chr22:27829200-27830000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr22:27829200-27830000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr22:27829200-27830000	Enhancers	Gastric	stomach

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