Variant report

Variant	nsv523038
Chromosome Location	chr21:47980570-47985655
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	BHLHE40	chr21:47984475-47984548	K562	blood:	n/a	n/a
2	BHLHE40	chr21:47983229-47983425	K562	blood:	n/a	n/a
3	CTCF	chr21:47980700-47980850	HepG2	liver:	n/a	n/a
4	EP300	chr21:47983034-47983824	ECC-1	luminal epithelium:	n/a	n/a
5	ESR1	chr21:47983264-47983558	ECC-1	luminal epithelium:	n/a	chr21:47983437-47983454
6	ESRRA	chr21:47979105-47980790	GM12878	blood:	n/a	chr21:47979782-47979792 chr21:47979785-47979797 chr21:47979785-47979795 chr21:47979778-47979791 chr21:47979781-47979797 chr21:47979775-47979791 chr21:47979779-47979789 chr21:47979779-47979791 chr21:47979784-47979797 chr21:47979785-47979795 chr21:47979779-47979789 chr21:47979788-47979798
7	FOS	chr21:47984265-47984577	MCF10A-Er-Src	breast:	n/a	chr21:47984416-47984423 chr21:47984416-47984424 chr21:47984415-47984425
8	FOS	chr21:47984325-47984582	MCF10A-Er-Src	breast:	n/a	chr21:47984416-47984423 chr21:47984416-47984424 chr21:47984415-47984425
9	FOS	chr21:47984271-47984582	MCF10A-Er-Src	breast:	n/a	chr21:47984416-47984423 chr21:47984416-47984424 chr21:47984415-47984425
10	FOS	chr21:47984346-47984496	MCF10A-Er-Src	breast:	n/a	chr21:47984416-47984423 chr21:47984416-47984424 chr21:47984415-47984425
11	JUND	chr21:47984321-47984550	HepG2	liver:	n/a	chr21:47984414-47984425 chr21:47984416-47984423 chr21:47984416-47984424 chr21:47984415-47984425
12	MAX	chr21:47983078-47983569	ECC-1	luminal epithelium:	n/a	chr21:47983407-47983417
13	MAX	chr21:47983114-47983639	ECC-1	luminal epithelium:	n/a	chr21:47983407-47983417
14	MAX	chr21:47983412-47983420	NB4	blood:	n/a	n/a
15	MYC	chr21:47983308-47983375	K562	blood:	n/a	n/a
16	MYC	chr21:47981365-47981479	HUVEC	blood vessel:	n/a	n/a
17	NFIC	chr21:47982910-47983832	ECC-1	luminal epithelium:	n/a	chr21:47983310-47983338 chr21:47983310-47983327 chr21:47983380-47983397 chr21:47983310-47983326
18	NFIC	chr21:47982903-47983766	ECC-1	luminal epithelium:	n/a	chr21:47983310-47983338 chr21:47983310-47983327 chr21:47983380-47983397 chr21:47983310-47983326
19	POLR2A	chr21:47982649-47982841	GM12878	blood:	n/a	n/a
20	POLR2A	chr21:47982494-47982663	HepG2	liver:	n/a	n/a
21	POLR2A	chr21:47982617-47982649	K562	blood:	n/a	n/a
22	POLR2A	chr21:47983030-47983161	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr21:47985032-47985219	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr21:47982426-47982518	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr21:47982331-47982527	K562	blood:	n/a	n/a
26	POLR2A	chr21:47984237-47984771	H1-neurons	neurons:	n/a	n/a
27	POLR2A	chr21:47984176-47984811	H1-neurons	neurons:	n/a	n/a
28	POLR2A	chr21:47983783-47983893	K562	blood:	n/a	n/a
29	POLR2A	chr21:47983221-47983463	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr21:47981069-47981094	K562	blood:	n/a	n/a
31	POLR2A	chr21:47981248-47981327	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr21:47983049-47983120	K562	blood:	n/a	n/a
33	POLR2A	chr21:47985109-47985145	MCF-7	breast:	n/a	n/a
34	POLR2A	chr21:47984132-47984278	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr21:47982086-47982164	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr21:47981344-47981441	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr21:47984594-47984653	K562	blood:	n/a	n/a
38	POLR2A	chr21:47982656-47982857	K562	blood:	n/a	n/a
39	POLR2A	chr21:47983390-47983406	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr21:47983772-47983798	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr21:47980675-47980726	ProgFib	skin:	n/a	n/a
42	POLR2A	chr21:47983009-47983584	HL-60	blood:	n/a	n/a
43	POLR2A	chr21:47983296-47983376	K562	blood:	n/a	n/a
44	POLR2A	chr21:47983221-47983422	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr21:47985149-47985161	MCF-7	breast:	n/a	n/a
46	POLR2A	chr21:47982476-47982580	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr21:47982409-47982592	K562	blood:	n/a	n/a
48	POLR2A	chr21:47982536-47982778	H1-hESC	embryonic stem cell:	n/a	n/a
49	RCOR1	chr21:47983234-47983269	Hela-S3	cervix:	n/a	n/a
50	REST	chr21:47984249-47984772	H1-neurons	neurons:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:47980561..47982874-chr21:47984744..47986654,2	MCF-7	breast:
2	chr21:47979855..47982153-chr21:48055162..48056734,2	MCF-7	breast:
3	chr21:47984970..47986522-chr21:48008602..48011495,2	K562	blood:
4	chr21:47972221..47973948-chr21:47980674..47982187,2	K562	blood:
5	chr21:47971877..47975830-chr21:47983188..47986029,3	K562	blood:
6	chr21:47974804..47979372-chr21:47979836..47984256,6	MCF-7	breast:
7	chr21:47877021..47880570-chr21:47984512..47987705,4	K562	blood:

Variant related genes	Relation type
DIP2A	TF binding region
ENSG00000160305	chromatin interactions
ENSG00000160310	chromatin interactions

Extended variants
information (count: 237 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:237 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2070429	chr21:47980570-47980571	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375179011	chr21:47980598-47980599	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs377438725	chr21:47980606-47980607	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs370283379	chr21:47980645-47980646	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs374726250	chr21:47980656-47980657	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs368863562	chr21:47980687-47980688	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs377051396	chr21:47980694-47980695	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs540571753	chr21:47980713-47980714	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs368596513	chr21:47980759-47980760	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs2839324	chr21:47980760-47980761	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs532417043	chr21:47980779-47980780	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs550985047	chr21:47980780-47980781	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs76005530	chr21:47980800-47980801	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
14	rs530177504	chr21:47980803-47980804	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs372337809	chr21:47980833-47980834	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs369015050	chr21:47980864-47980865	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs116695953	chr21:47980865-47980866	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs2839325	chr21:47980913-47980914	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs191865138	chr21:47980930-47980931	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570395749	chr21:47980942-47980943	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs34529071	chr21:47980948-47980949	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs556152926	chr21:47980952-47980953	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs574583127	chr21:47980970-47980971	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs535552003	chr21:47980979-47980980	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs555152886	chr21:47980982-47980983	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs147393304	chr21:47980991-47980992	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs139810929	chr21:47981021-47981022	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145296731	chr21:47981034-47981035	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577492555	chr21:47981058-47981059	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs550937109	chr21:47981064-47981065	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs182891305	chr21:47981074-47981075	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs562581020	chr21:47981090-47981091	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs530096305	chr21:47981103-47981104	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs11910673	chr21:47981158-47981159	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs559888307	chr21:47981214-47981215	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs527498722	chr21:47981241-47981242	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs369201377	chr21:47981254-47981255	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs552385525	chr21:47981265-47981266	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs118052415	chr21:47981301-47981302	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs185279028	chr21:47981346-47981347	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs571336854	chr21:47981379-47981380	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs373214438	chr21:47981414-47981415	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs532071301	chr21:47981442-47981443	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs568064361	chr21:47981456-47981457	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs535512950	chr21:47981465-47981466	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs553917820	chr21:47981466-47981467	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs565811854	chr21:47981473-47981474	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs374720753	chr21:47981490-47981491	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs369337407	chr21:47981539-47981540	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs190432938	chr21:47981565-47981566	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47943600-47990600	Strong transcription	Fetal Stomach	stomach
2	chr21:47947600-47989000	Strong transcription	Dnd41	blood
3	chr21:47947600-47991000	Strong transcription	Fetal Muscle Leg	muscle
4	chr21:47948400-47993600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr21:47948600-47993200	Strong transcription	Fetal Intestine Large	intestine
6	chr21:47949000-47988200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr21:47949000-47993600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr21:47949800-47991800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr21:47950000-47989200	Strong transcription	Skeletal Muscle Female	skeletal muscle
10	chr21:47950000-47991000	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr21:47950200-47993200	Strong transcription	Stomach Smooth Muscle	stomach
12	chr21:47953000-47988200	Strong transcription	Gastric	stomach
13	chr21:47953000-47988600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr21:47953200-47983400	Strong transcription	Brain Inferior Temporal Lobe	brain
15	chr21:47953200-47988400	Strong transcription	Fetal Intestine Small	intestine
16	chr21:47953200-47993000	Strong transcription	Osteobl	bone
17	chr21:47953400-47988000	Strong transcription	Cortex derived primary cultured neurospheres	brain
18	chr21:47956200-48001800	Weak transcription	Stomach Mucosa	stomach
19	chr21:47959200-47983400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr21:47961600-47992800	Strong transcription	Brain Hippocampus Middle	brain
21	chr21:47964600-47988400	Strong transcription	Brain Germinal Matrix	brain
22	chr21:47965200-47991200	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr21:47965800-47988600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr21:47965800-47993400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr21:47966200-47993400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr21:47966400-47987800	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr21:47966600-47988200	Strong transcription	Esophagus	oesophagus
28	chr21:47966800-47985400	Strong transcription	HMEC	breast
29	chr21:47966800-47985800	Weak transcription	K562	blood
30	chr21:47967400-47994800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr21:47968600-47990800	Strong transcription	Fetal Brain Female	brain
32	chr21:47969400-47987600	Strong transcription	Aorta	Aorta
33	chr21:47969600-47988200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr21:47969600-47988400	Strong transcription	Colonic Mucosa	Colon
35	chr21:47969800-47989200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr21:47970200-47992400	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr21:47970400-47988200	Strong transcription	Placenta Amnion	Placenta Amnion
38	chr21:47970400-47993200	Strong transcription	Brain Cingulate Gyrus	brain
39	chr21:47971000-47989200	Strong transcription	Placenta	Placenta
40	chr21:47971600-47991600	Strong transcription	Brain Substantia Nigra	brain
41	chr21:47972000-47988800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr21:47973200-47993000	Strong transcription	Duodenum Mucosa	Duodenum
43	chr21:47973400-47993200	Strong transcription	Rectal Smooth Muscle	rectum
44	chr21:47973600-47989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr21:47973600-47990600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr21:47973600-47991600	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr21:47973600-47992600	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr21:47973800-47983200	Strong transcription	Primary neutrophils fromperipheralblood	blood
49	chr21:47973800-47984200	Strong transcription	Brain Angular Gyrus	brain
50	chr21:47973800-47990600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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