Variant report

Variant	nsv1065433
Chromosome Location	chr21:15484229-15528702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:425)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr21:15488328-15488936	GM12878	blood:	n/a	n/a
2	BCL11A	chr21:15486659-15486847	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr21:15492361-15492757	GM12878	blood:	n/a	n/a
4	BCLAF1	chr21:15488385-15488957	GM12878	blood:	n/a	n/a
5	BHLHE40	chr21:15488497-15488954	GM12878	blood:	n/a	n/a
6	BHLHE40	chr21:15492443-15492754	GM12878	blood:	n/a	n/a
7	BRCA1	chr21:15492774-15492860	GM12878	blood:	n/a	n/a
8	CEBPB	chr21:15510869-15511102	HepG2	liver:	n/a	chr21:15510993-15511004
9	CHD1	chr21:15488594-15488710	GM12878	blood:	n/a	n/a
10	CHD2	chr21:15486580-15486971	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr21:15488403-15488850	GM12878	blood:	n/a	n/a
12	CTCF	chr21:15492500-15492650	HPF	lung:	n/a	n/a
13	CTCF	chr21:15492513-15492641	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr21:15492540-15492690	HMF	breast:	n/a	n/a
15	CTCF	chr21:15492520-15492670	HVMF	connective:	n/a	n/a
16	CTCF	chr21:15491420-15491570	BE2_C	brain:	n/a	n/a
17	CTCF	chr21:15491520-15491590	HepG2	liver:	n/a	n/a
18	CTCF	chr21:15491520-15491670	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr21:15492480-15492630	HCM	heart:	n/a	n/a
20	CTCF	chr21:15512070-15512090	GM20000	blood:	n/a	n/a
21	CTCF	chr21:15492480-15492630	SAEC	small airway:	n/a	n/a
22	CTCF	chr21:15492444-15492765	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr21:15492520-15492670	BJ	skin:	n/a	n/a
24	CTCF	chr21:15491595-15491604	HepG2	liver:	n/a	n/a
25	CTCF	chr21:15491440-15491590	GM12864	blood:	n/a	n/a
26	CTCF	chr21:15492540-15492690	HMEC	breast:	n/a	n/a
27	CTCF	chr21:15492303-15492333	Lung_OC	lung:	n/a	n/a
28	CTCF	chr21:15492540-15492690	AG04449	skin:	n/a	n/a
29	CTCF	chr21:15492540-15492690	AG09309	skin:	n/a	n/a
30	CTCF	chr21:15492520-15492670	A549	lung:	n/a	n/a
31	CTCF	chr21:15492540-15492690	K562	blood:	n/a	n/a
32	CTCF	chr21:15492461-15492757	HepG2	liver:	n/a	n/a
33	CTCF	chr21:15492540-15492690	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr21:15491387-15491741	K562	blood:	n/a	n/a
35	CTCF	chr21:15492525-15492726	Lung_OC	lung:	n/a	n/a
36	CTCF	chr21:15492470-15492756	K562	blood:	n/a	n/a
37	CTCF	chr21:15491391-15491705	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr21:15492520-15492670	GM12871	blood:	n/a	n/a
39	CTCF	chr21:15492560-15492710	HAc	cerebellar:	n/a	n/a
40	CTCF	chr21:15492540-15492690	HCT-116	colon:	n/a	n/a
41	CTCF	chr21:15492510-15492654	HepG2	liver:	n/a	n/a
42	CTCF	chr21:15492560-15492710	HFF	foreskin:	n/a	n/a
43	CTCF	chr21:15491520-15491614	ProgFib	skin:	n/a	n/a
44	CTCF	chr21:15492540-15492690	BJ	skin:	n/a	n/a
45	CTCF	chr21:15491500-15491650	HEK293	kidney:	n/a	n/a
46	CTCF	chr21:15492520-15492670	GM12870	blood:	n/a	n/a
47	CTCF	chr21:15492500-15492650	HEK293	kidney:	n/a	n/a
48	CTCF	chr21:15491406-15491651	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr21:15492520-15492670	NB4	blood:	n/a	n/a
50	CTCF	chr21:15492400-15492550	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15487742-15487792	GM12892	blood:	n/a
2	chr21:15487742-15487792	LNCaP	prostate:	n/a
3	chr21:15487742-15487792	GM12878	blood:	n/a
4	chr21:15487742-15487792	GM19239	blood:	n/a
5	chr21:15487742-15487792	PrEC	prostate:	n/a
6	chr21:15487742-15487792	RPTEC	kidney:	n/a
7	chr21:15487742-15487792	AG10803	skin:	n/a
8	chr21:15487742-15487792	AoSMC	blood vessel:	n/a
9	chr21:15487742-15487792	HCT-116	colon:	n/a
10	chr21:15487742-15487792	HEK293	kidney:	embryo
11	chr21:15487742-15487792	NHBE	bronchial:	n/a
12	chr21:15487742-15487792	SAEC	small airway:	n/a
13	chr21:15487742-15487792	HEEpiC	esophagus:	n/a
14	chr21:15487742-15487792	HPAEpiC	pulmonary alveolar:	n/a
15	chr21:15487742-15487792	HRE	kidney:	n/a
16	chr21:15487742-15487792	NT2-D1	testis:	n/a
17	chr21:15487742-15487792	K562	blood:	n/a
18	chr21:15487742-15487792	NHDF-neo	bronchial:	n/a
19	chr21:15487742-15487792	U87	brain:	n/a
20	chr21:15487742-15487792	PANC-1	pancreas:	n/a
21	chr21:15487742-15487792	AG04450	lung:	fetal
22	chr21:15487742-15487792	HIPEpiC	eye:	n/a
23	chr21:15487742-15487792	BJ	skin:	n/a
24	chr21:15487742-15487792	GM06990	blood:	n/a
25	chr21:15487742-15487792	SK-N-SH_RA	brain:	n/a
26	chr21:15487742-15487792	AG09309	skin:	n/a
27	chr21:15487742-15487792	HRCEpiC	kidney:	n/a
28	chr21:15487742-15487792	PFSK-1	brain:	n/a
29	chr21:15487742-15487792	SKMC	muscle:	n/a
30	chr21:15487742-15487792	ECC-1	luminal epithelium:	n/a
31	chr21:15487742-15487792	HAEpiC	amniotic membrane:	n/a
32	chr21:15487742-15487792	NH-A	brain:	n/a
33	chr21:15487742-15487792	SK-N-MC	brain:	n/a
34	chr21:15487742-15487792	NB4	blood:	n/a
35	chr21:15487742-15487792	Hela-S3	cervix:	n/a
36	chr21:15487742-15487792	AG04449	skin:	fetal
37	chr21:15487742-15487792	Jurkat	blood:	n/a
38	chr21:15487742-15487792	GM12891	blood:	n/a
39	chr21:15487742-15487792	IMR90	lung:	fetal
40	chr21:15487742-15487792	T-47D	breast:	n/a
41	chr21:15487742-15487792	MCF10A-Er-Src	breast:	n/a
42	chr21:15487742-15487792	H1-hESC	embryonic stem cell:	embryo
43	chr21:15487742-15487792	HepG2	liver:	n/a
44	chr21:15487742-15487792	HNPCEpiC	eye:	n/a
45	chr21:15487742-15487792	CMK	blood:	n/a
46	chr21:15487742-15487792	SK-N-SH	brain:	n/a
47	chr21:15487742-15487792	HCPEpiC	choroid plexus:	n/a
48	chr21:15487742-15487792	HRPEpiC	eye:	n/a
49	chr21:15487742-15487792	Caco-2	colon:	n/a
50	chr21:15487742-15487792	A549	lung:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15510246..15512237-chr21:15537714..15540194,2	MCF-7	breast:
2	chr21:15498829..15500815-chr21:15502377..15504055,2	K562	blood:
3	chr21:15518340..15522108-chr21:15524344..15527724,3	K562	blood:
4	chr21:15518340..15522108-chr21:15524344..15527724,3	K562	blood:
5	chr21:15493769..15495607-chr21:15500118..15502421,2	K562	blood:
6	chr21:15498829..15500815-chr21:15502377..15504055,2	K562	blood:
7	chr10:43144345..43147006-chr21:15489906..15492564,2	K562	blood:
8	chr21:15493769..15495607-chr21:15500118..15502421,2	K562	blood:
9	chr21:15494107..15496665-chr21:15500921..15502468,2	K562	blood:
10	chr21:15525627..15528349-chr21:15528891..15531614,2	K562	blood:
11	chr21:15494107..15496665-chr21:15500921..15502468,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-2	chr21:15515902-15516479	NONHSAT081148

No data

Variant related genes	Relation type
ERLEC1P1	TF binding region
ERLEC1P1	CpG island

Extended variants
information (count: 639 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554327435	chr21:15484229-15484230	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs370243030	chr21:15484264-15484265	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs545546715	chr21:15484272-15484273	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs536320137	chr21:15484311-15484312	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs556156274	chr21:15484312-15484313	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs377197214	chr21:15484409-15484410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374507143	chr21:15484421-15484422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565609842	chr21:15484438-15484439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74666896	chr21:15484441-15484442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9982308	chr21:15484493-15484494	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs35152122	chr21:15484520-15484521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577861333	chr21:15484541-15484542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540089810	chr21:15484590-15484591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140837040	chr21:15484592-15484593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144683862	chr21:15484597-15484598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556298303	chr21:15484619-15484620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540113605	chr21:15484671-15484672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147899786	chr21:15484744-15484745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373258002	chr21:15484786-15484787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75181276	chr21:15484838-15484839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551347886	chr21:15484872-15484873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565473029	chr21:15484896-15484897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144576171	chr21:15484936-15484937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146528452	chr21:15484938-15484939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148407946	chr21:15484939-15484940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs55827840	chr21:15484940-15484941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200873700	chr21:15484941-15484942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527963534	chr21:15484958-15484959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547696847	chr21:15484979-15484980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182513822	chr21:15485003-15485004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370654669	chr21:15485046-15485047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375245849	chr21:15485085-15485086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139269641	chr21:15485129-15485130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367979836	chr21:15485161-15485162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187259347	chr21:15485212-15485213	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569814095	chr21:15485219-15485220	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149983276	chr21:15485299-15485300	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558896747	chr21:15485342-15485343	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145431619	chr21:15485352-15485353	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534055985	chr21:15485370-15485371	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554017761	chr21:15485404-15485405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192028411	chr21:15485427-15485428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184667615	chr21:15485436-15485437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542837492	chr21:15485487-15485488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562612232	chr21:15485501-15485502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575870165	chr21:15485564-15485565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190549445	chr21:15485575-15485576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149207606	chr21:15485586-15485587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527993252	chr21:15485612-15485613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549614845	chr21:15485738-15485739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15457600-15487400	Weak transcription	Fetal Brain Male	brain
2	chr21:15457800-15486200	Weak transcription	Thymus	Thymus
3	chr21:15470400-15487200	Weak transcription	Ovary	ovary
4	chr21:15470800-15484800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr21:15470800-15486200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr21:15474000-15489200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr21:15474600-15489600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr21:15475000-15486600	Weak transcription	Fetal Stomach	stomach
9	chr21:15475400-15485200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr21:15475800-15494600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr21:15477600-15498000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr21:15478000-15495200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr21:15479600-15485200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr21:15480400-15497200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr21:15483200-15485000	Weak transcription	Dnd41	blood
16	chr21:15483200-15485400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr21:15484200-15484400	ZNF genes & repeats	Fetal Brain Female	brain
18	chr21:15485000-15488600	Strong transcription	Dnd41	blood
19	chr21:15485200-15485400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr21:15485200-15486200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr21:15485400-15486000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr21:15485400-15486400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr21:15485800-15486600	Weak transcription	GM12878-XiMat	blood
24	chr21:15486000-15494000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr21:15486200-15487200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr21:15486200-15496600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr21:15486600-15486800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr21:15486600-15487000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr21:15486600-15487000	Enhancers	Esophagus	oesophagus
30	chr21:15486600-15487000	ZNF genes & repeats	Fetal Stomach	stomach
31	chr21:15486600-15487000	ZNF genes & repeats	GM12878-XiMat	blood
32	chr21:15486600-15487000	Enhancers	HMEC	breast
33	chr21:15486600-15487200	Enhancers	Placenta	Placenta
34	chr21:15486600-15487600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr21:15486800-15487000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr21:15487000-15487200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr21:15487000-15487800	Weak transcription	Esophagus	oesophagus
38	chr21:15487000-15487800	Weak transcription	Fetal Stomach	stomach
39	chr21:15487000-15487800	Weak transcription	GM12878-XiMat	blood
40	chr21:15487000-15488000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr21:15487200-15488000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr21:15487400-15489600	Enhancers	Primary B cells from peripheral blood	blood
43	chr21:15487800-15488000	Enhancers	GM12878-XiMat	blood
44	chr21:15487800-15488600	Strong transcription	Fetal Stomach	stomach
45	chr21:15487800-15489000	Enhancers	Esophagus	oesophagus
46	chr21:15488000-15488200	Flanking Active TSS	GM12878-XiMat	blood
47	chr21:15488000-15488600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr21:15488000-15488800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr21:15488200-15488400	Enhancers	GM12878-XiMat	blood
50	chr21:15488200-15488600	Weak transcription	Gastric	stomach

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