Variant report

Variant	rs34239371
Chromosome Location	chr21:45876065-45876066
allele	C/T
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	GABPA	chr21:45875862-45876159	H1-hESC	embryonic stem cell:	n/a	n/a
2	ZNF143	chr21:45875833-45876081	Hela-S3	cervix:	n/a	chr21:45876066-45876076
3	USF1	chr21:45875807-45876126	A549	lung:	n/a	chr21:45875950-45875961
4	CTCF	chr21:45875820-45876076	LNCaP	prostate:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
5	MAX	chr21:45875688-45876238	ECC-1	luminal epithelium:	n/a	chr21:45875953-45875960 chr21:45875951-45875961 chr21:45875951-45875962 chr21:45875952-45875961 chr21:45875950-45875963 chr21:45875951-45875962 chr21:45876031-45876041 chr21:45875952-45875961 chr21:45875952-45875962
6	CTCF	chr21:45875839-45876079	GM19239	blood:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
7	HA-E2F1	chr21:45875614-45876165	MCF-7	breast:	n/a	chr21:45875798-45875805
8	CTCF	chr21:45875815-45876073	A549	lung:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
9	CTCF	chr21:45875560-45876371	SK-N-SH	brain:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
10	USF1	chr21:45875831-45876096	H1-hESC	embryonic stem cell:	n/a	chr21:45875950-45875961
11	CTCF	chr21:45875813-45876079	MCF-7	breast:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
12	CTCF	chr21:45875810-45876087	ProgFib	skin:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
13	ZBTB7A	chr21:45875323-45876135	ECC-1	luminal epithelium:	n/a	chr21:45875934-45875943
14	CTCF	chr21:45875805-45876099	MCF-7	breast:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
15	CTCF	chr21:45875810-45876095	MCF-7	breast:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
16	GABPA	chr21:45875873-45876114	H1-hESC	embryonic stem cell:	n/a	n/a
17	RAD21	chr21:45875748-45876090	A549	lung:	n/a	chr21:45875935-45875949
18	MAX	chr21:45875717-45876271	HepG2	liver:	n/a	chr21:45875953-45875960 chr21:45875951-45875961 chr21:45875951-45875962 chr21:45875952-45875961 chr21:45875950-45875963 chr21:45875951-45875962 chr21:45876031-45876041 chr21:45875952-45875961 chr21:45875952-45875962
19	RAD21	chr21:45875796-45876068	H1-hESC	embryonic stem cell:	n/a	chr21:45875935-45875949
20	USF2	chr21:45875825-45876080	Hela-S3	cervix:	n/a	chr21:45875950-45875961
21	MAX	chr21:45875612-45876431	H1-hESC	embryonic stem cell:	n/a	chr21:45875953-45875960 chr21:45875951-45875961 chr21:45875951-45875962 chr21:45875952-45875961 chr21:45875950-45875963 chr21:45875951-45875962 chr21:45876031-45876041 chr21:45875952-45875961 chr21:45875952-45875962
22	CTCF	chr21:45875835-45876071	GM19240	blood:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
23	E2F6	chr21:45875615-45876202	H1-hESC	embryonic stem cell:	n/a	chr21:45875798-45875805
24	CTCF	chr21:45875788-45876102	GM12878	blood:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
25	CTCF	chr21:45875812-45876096	GM19238	blood:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
26	MAX	chr21:45875786-45876076	H1-hESC	embryonic stem cell:	n/a	chr21:45875953-45875960 chr21:45875951-45875961 chr21:45875951-45875962 chr21:45875952-45875961 chr21:45875950-45875963 chr21:45875951-45875962 chr21:45876031-45876041 chr21:45875952-45875961 chr21:45875952-45875962
27	USF1	chr21:45875753-45876125	A549	lung:	n/a	chr21:45875950-45875961
28	RAD21	chr21:45875758-45876240	MCF-7	breast:	n/a	chr21:45876142-45876154 chr21:45875935-45875949 chr21:45876144-45876154
29	SMC3	chr21:45875752-45876139	Hela-S3	cervix:	n/a	chr21:45875935-45875945
30	MAX	chr21:45875541-45876255	MCF-7	breast:	n/a	chr21:45875545-45875555 chr21:45875953-45875960 chr21:45875951-45875961 chr21:45875951-45875962 chr21:45875952-45875961 chr21:45875950-45875963 chr21:45875951-45875962 chr21:45876031-45876041 chr21:45875952-45875961 chr21:45875952-45875962 chr21:45875593-45875603
31	USF2	chr21:45875813-45876099	H1-hESC	embryonic stem cell:	n/a	chr21:45875950-45875961
32	HDAC2	chr21:45875626-45876557	MCF-7	breast:	n/a	n/a
33	RAD21	chr21:45875678-45876166	H1-hESC	embryonic stem cell:	n/a	chr21:45876142-45876154 chr21:45875935-45875949 chr21:45876144-45876154
34	MAX	chr21:45875572-45876249	HCT-116	colon:	n/a	chr21:45875953-45875960 chr21:45875951-45875961 chr21:45875951-45875962 chr21:45875952-45875961 chr21:45875950-45875963 chr21:45875951-45875962 chr21:45876031-45876041 chr21:45875952-45875961 chr21:45875952-45875962 chr21:45875593-45875603
35	CTCF	chr21:45875920-45876070	GM12864	blood:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
36	RAD21	chr21:45875568-45876294	SK-N-SH	brain:	n/a	chr21:45876142-45876154 chr21:45875935-45875949 chr21:45876144-45876154
37	CTCF	chr21:45875828-45876074	GM10266	blood:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
38	USF1	chr21:45875828-45876081	SK-N-SH_RA	brain:	n/a	chr21:45875950-45875961
39	CTCF	chr21:45875815-45876086	Fibrobl	skin:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
40	CTCF	chr21:45875825-45876072	HepG2	liver:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
41	USF1	chr21:45875716-45876142	ECC-1	luminal epithelium:	n/a	chr21:45875950-45875961
42	MAX	chr21:45875629-45876264	HCT-116	colon:	n/a	chr21:45875953-45875960 chr21:45875951-45875961 chr21:45875951-45875962 chr21:45875952-45875961 chr21:45875950-45875963 chr21:45875951-45875962 chr21:45876031-45876041 chr21:45875952-45875961 chr21:45875952-45875962
43	CTCF	chr21:45875749-45876103	A549	lung:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
44	CTCF	chr21:45875860-45876150	GM12871	blood:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
45	E2F6	chr21:45875829-45876157	A549	lung:	n/a	n/a
46	USF1	chr21:45875692-45876182	HCT-116	colon:	n/a	chr21:45875950-45875961
47	CTCF	chr21:45875837-45876068	MCF-7	breast:	n/a	chr21:45875935-45875948 chr21:45875936-45875946
48	RAD21	chr21:45875725-45876105	Hela-S3	cervix:	n/a	chr21:45875935-45875949
49	MAX	chr21:45875759-45876084	SK-N-SH	brain:	n/a	chr21:45875953-45875960 chr21:45875951-45875961 chr21:45875951-45875962 chr21:45875952-45875961 chr21:45875950-45875963 chr21:45875951-45875962 chr21:45876031-45876041 chr21:45875952-45875961 chr21:45875952-45875962
50	CTCF	chr21:45875704-45876079	MCF-7	breast:	n/a	chr21:45875935-45875948 chr21:45875936-45875946

No.	Distal block	Cell Line	Cell type
1	chr21:45874301..45877175-chr21:45878479..45881429,3	MCF-7	breast:
2	chr21:45875711..45878548-chr21:45899746..45901735,2	MCF-7	breast:
3	chr21:45719757..45722045-chr21:45874863..45877372,2	MCF-7	breast:
4	chr21:45756335..45760049-chr21:45874026..45878349,7	MCF-7	breast:
5	chr21:45875830..45876432-chr21:45929281..45929900,2	MCF-7	breast:
6	chr21:45875495..45879436-chr21:45881615..45885234,3	K562	blood:

Variant related genes	Relation type
LRRC3DN	TF binding region
LRRC3-AS1	TF binding region
ENSG00000232969	Chromatin interaction
ENSG00000160226	Chromatin interaction
ENSG00000269430	Chromatin interaction
ENSG00000141959	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1007440	0.94[EUR][1000 genomes]
rs11088953	0.99[EUR][1000 genomes]
rs1573340	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1984324	0.81[EUR][1000 genomes]
rs1984325	0.81[EUR][1000 genomes]
rs1984326	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2011324	0.91[EUR][1000 genomes]
rs2155726	0.92[EUR][1000 genomes]
rs2186932	0.94[EUR][1000 genomes]
rs2236672	0.92[EUR][1000 genomes]
rs2329780	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2838561	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2838562	0.92[EUR][1000 genomes]
rs36011733	0.86[EUR][1000 genomes]
rs3804034	0.89[EUR][1000 genomes]
rs4818921	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4818922	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4818925	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6518188	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6518189	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6518192	0.82[EUR][1000 genomes]
rs762430	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8128434	0.91[ASN][1000 genomes]
rs915781	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9306101	0.92[EUR][1000 genomes]
rs9306103	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9306104	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9975657	0.86[EUR][1000 genomes]
rs9978193	0.94[EUR][1000 genomes]
rs9978219	0.92[EUR][1000 genomes]
rs9981271	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9982752	0.89[EUR][1000 genomes]
rs9983377	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33817	chr21:45169412-46031810	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv913898	chr21:45555079-45941566	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
3	esv3361489	chr21:45669073-46013747	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	69 gene(s)	inside rSNPs	diseases
4	nsv913911	chr21:45681153-45893907	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
5	nsv913918	chr21:45697755-45941566	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
6	nsv913922	chr21:45699404-45893907	Genic enhancers Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
7	nsv913930	chr21:45700641-45893907	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
8	nsv913940	chr21:45712588-45893907	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
9	nsv913941	chr21:45722442-45885589	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
10	nsv1058359	chr21:45724055-45941566	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
11	nsv1065203	chr21:45731690-45941566	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
12	nsv544473	chr21:45731690-45941566	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
13	nsv913942	chr21:45740823-45941566	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
14	nsv913943	chr21:45740823-46031810	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
15	nsv1067264	chr21:45757599-45941566	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
16	nsv544474	chr21:45757599-45941566	Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
17	nsv913944	chr21:45757905-45941566	Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
18	nsv1058534	chr21:45812976-45916560	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
19	nsv587801	chr21:45832912-45916560	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
20	nsv913945	chr21:45837433-45893907	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
21	nsv913946	chr21:45838632-46031810	Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
22	nsv913947	chr21:45852949-45885589	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
23	nsv913948	chr21:45860912-46031810	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
24	nsv834109	chr21:45869352-45916560	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
25	esv3362556	chr21:45874049-45876897	Enhancers Genic enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
26	esv3395562	chr21:45874349-45876522	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45873800-45876800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr21:45874400-45876600	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr21:45874600-45876200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr21:45874600-45876200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr21:45874600-45876200	Active TSS	H9 Cell Line	embryonic stem cell
6	chr21:45874600-45876200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
7	chr21:45874600-45876400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr21:45874600-45876600	Active TSS	Rectal Smooth Muscle	rectum
9	chr21:45874800-45876200	Active TSS	Aorta	Aorta
10	chr21:45875000-45876200	Active TSS	Psoas Muscle	Psoas
11	chr21:45875000-45876400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr21:45875000-45876400	Active TSS	A549	lung
13	chr21:45875200-45876200	Active TSS	Fetal Intestine Large	intestine
14	chr21:45875400-45876200	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr21:45875400-45876200	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr21:45875400-45876200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
17	chr21:45875400-45876200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr21:45875400-45876200	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
19	chr21:45875400-45876200	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr21:45875400-45876200	Active TSS	Rectal Mucosa Donor 31	rectum
21	chr21:45875400-45876200	Active TSS	HSMM	muscle
22	chr21:45875400-45876200	Active TSS	NHEK	skin
23	chr21:45875400-45876400	Flanking Active TSS	Primary hematopoietic stem cells	blood
24	chr21:45875400-45876400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr21:45875400-45876600	Active TSS	Colon Smooth Muscle	Colon
26	chr21:45875600-45876200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
27	chr21:45875600-45876200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr21:45875600-45876200	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr21:45875600-45876200	Active TSS	NHDF-Ad	bronchial
30	chr21:45875600-45876400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr21:45875600-45876400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
32	chr21:45875600-45876400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr21:45875600-45876400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
34	chr21:45875600-45876400	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr21:45875600-45877400	Enhancers	Fetal Brain Male	brain
36	chr21:45875800-45876200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr21:45875800-45876200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
38	chr21:45875800-45876200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
39	chr21:45875800-45876200	Flanking Active TSS	Primary B cells from peripheral blood	blood
40	chr21:45875800-45876200	Flanking Active TSS	Primary T cells from cord blood	blood
41	chr21:45875800-45876200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr21:45875800-45876200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
43	chr21:45875800-45876200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr21:45875800-45876200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr21:45875800-45876200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr21:45875800-45876200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr21:45875800-45876200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
48	chr21:45875800-45876200	Flanking Active TSS	Esophagus	oesophagus
49	chr21:45875800-45876200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
50	chr21:45875800-45876200	Flanking Active TSS	Left Ventricle	heart

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