Variant report

Variant	rs73793383
Chromosome Location	chr4:1359604-1359605
allele	A/G
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	CTCF	chr4:1359520-1359670	Caco-2	colon:	n/a	n/a
2	CTCF	chr4:1359392-1359978	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr4:1359540-1359690	Caco-2	colon:	n/a	n/a
4	CTCF	chr4:1359576-1359839	GM19239	blood:	n/a	n/a
5	CTCF	chr4:1359540-1359690	GM12864	blood:	n/a	n/a
6	RAD21	chr4:1359388-1360012	MCF-7	breast:	n/a	chr4:1359806-1359825
7	CTCF	chr4:1359479-1359685	HepG2	liver:	n/a	n/a
8	MYC	chr4:1359471-1359835	MCF-7	breast:	n/a	n/a
9	CTCF	chr4:1359478-1359907	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr4:1359443-1359903	MCF-7	breast:	n/a	n/a
11	SIN3AK20	chr4:1359184-1360004	MCF-7	breast:	n/a	n/a
12	RAD21	chr4:1359521-1359936	H1-hESC	embryonic stem cell:	n/a	chr4:1359806-1359825
13	CTCF	chr4:1359500-1359650	GM12866	blood:	n/a	n/a
14	ZNF217	chr4:1359541-1359856	MCF-7	breast:	n/a	n/a
15	TCF12	chr4:1359224-1360034	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:1359580-1359730	GM12872	blood:	n/a	n/a
17	GATA3	chr4:1359430-1359946	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:1359560-1359710	GM12864	blood:	n/a	n/a
19	NR3C1	chr4:1359303-1359604	ECC-1	luminal epithelium:	n/a	chr4:1359438-1359452 chr4:1359437-1359453 chr4:1359436-1359454 chr4:1359437-1359453 chr4:1359438-1359452 chr4:1359437-1359454 chr4:1359437-1359453 chr4:1359434-1359455 chr4:1359437-1359453
20	CTCF	chr4:1359461-1359914	MCF-7	breast:	n/a	n/a
21	CTCF	chr4:1359600-1359750	NHEK	skin:	n/a	n/a
22	MAX	chr4:1359257-1359973	MCF-7	breast:	n/a	n/a
23	MYC	chr4:1359512-1359774	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:1359474-1359919	MCF-7	breast:	n/a	n/a
25	TCF12	chr4:1359455-1359904	H1-hESC	embryonic stem cell:	n/a	n/a
26	RAD21	chr4:1359502-1360116	HCT-116	colon:	n/a	chr4:1359806-1359825 chr4:1360037-1360049
27	CTCF	chr4:1359560-1359710	GM12878	blood:	n/a	n/a
28	CTCF	chr4:1359330-1360206	HCT-116	colon:	n/a	n/a
29	CTCF	chr4:1359546-1359874	NHEK	skin:	n/a	n/a
30	RAD21	chr4:1359508-1359953	H1-hESC	embryonic stem cell:	n/a	chr4:1359806-1359825
31	CTCF	chr4:1359470-1360021	HCT-116	colon:	n/a	n/a
32	GATA3	chr4:1359461-1359787	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:1359454-1359922	MCF-7	breast:	n/a	n/a
34	RAD21	chr4:1359382-1360055	H1-hESC	embryonic stem cell:	n/a	chr4:1359806-1359825 chr4:1360037-1360049
35	HA-E2F1	chr4:1359419-1360035	MCF-7	breast:	n/a	n/a
36	TCF12	chr4:1359458-1359757	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:1359534-1359846	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:1359406-1359975	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:1359540-1359810	GM06990	blood:	n/a	n/a
40	CTCF	chr4:1359523-1359890	GM12891	blood:	n/a	n/a
41	CTCF	chr4:1359593-1359902	GM12878	blood:	n/a	n/a
42	CTCF	chr4:1359549-1359961	K562	blood:	n/a	n/a
43	CTCF	chr4:1359600-1359750	HRE	kidney:	n/a	n/a
44	CTCF	chr4:1359480-1359630	GM12872	blood:	n/a	n/a
45	CTCF	chr4:1359599-1359854	A549	lung:	n/a	n/a
46	CTCF	chr4:1359447-1359897	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr4:1359448-1359919	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:1359581-1359629	GM12878	blood:	n/a	n/a
49	POLR2A	chr4:1359503-1359795	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:1359480-1359630	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:1349932..1350910-chr4:1359199..1360093,5	MCF-7	breast:
2	chr4:1004206..1006637-chr4:1357918..1359742,2	MCF-7	breast:
3	chr4:1339729..1343240-chr4:1359477..1362445,4	MCF-7	breast:
4	chr4:1052002..1052766-chr4:1359397..1360108,2	MCF-7	breast:
5	chr4:1241603..1244374-chr4:1357960..1359883,2	MCF-7	breast:

Variant related genes	Relation type
UVSSA	TF binding region
ENSG00000163945	Chromatin interaction
ENSG00000127418	Chromatin interaction
ENSG00000254094	Chromatin interaction
ENSG00000178222	Chromatin interaction
ENSG00000196810	Chromatin interaction
ENSG00000159692	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11726178	0.86[ASN][1000 genomes]
rs11726179	0.86[ASN][1000 genomes]
rs11945799	0.93[ASN][1000 genomes]
rs12501056	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17164682	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1882099	0.88[ASN][1000 genomes]
rs2276904	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3749456	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3806754	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4974557	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4974600	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs58552306	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60682925	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61073965	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6810729	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6852717	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73075548	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73075553	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73793390	0.93[ASN][1000 genomes]
rs73793392	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7667152	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
2	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
3	esv3339080	chr4:970630-1546223	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv878328	chr4:1141573-1990425	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer 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 miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
5	nsv878330	chr4:1147407-1523930	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
6	nsv461152	chr4:1159680-1415698	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
7	nsv593278	chr4:1159680-1415698	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
8	nsv997971	chr4:1191256-1518521	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
9	nsv878339	chr4:1277826-1363886	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
10	nsv878340	chr4:1277826-1386570	Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
11	nsv878341	chr4:1277826-1391400	Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
12	nsv1002635	chr4:1282603-1402761	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
13	nsv878342	chr4:1291337-1363886	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
14	nsv878343	chr4:1291337-1391400	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv878344	chr4:1291337-1414684	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv878345	chr4:1291337-1563920	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
17	nsv878346	chr4:1300077-1363886	Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
18	nsv878347	chr4:1300077-1866358	Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
19	nsv878348	chr4:1305269-1386570	Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
20	esv1794294	chr4:1307119-1817474	Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
21	nsv878349	chr4:1318132-1363886	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
22	nsv878350	chr4:1320023-1500753	Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
23	nsv932661	chr4:1324751-1364014	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
24	nsv878351	chr4:1329847-1414684	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
25	nsv878352	chr4:1334721-1363886	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
26	nsv1008785	chr4:1335089-1518521	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
27	nsv536988	chr4:1335089-1518521	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
28	nsv593302	chr4:1338618-1414684	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1341800-1387800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:1341800-1388800	Weak transcription	Small Intestine	intestine
3	chr4:1342200-1369800	Weak transcription	HSMMtube	muscle
4	chr4:1342200-1382600	Weak transcription	Primary B cells from cord blood	blood
5	chr4:1342400-1370000	Weak transcription	HSMM	muscle
6	chr4:1342400-1379800	Weak transcription	A549	lung
7	chr4:1342600-1367200	Weak transcription	Hela-S3	cervix
8	chr4:1342600-1385600	Weak transcription	Fetal Kidney	kidney
9	chr4:1342800-1360400	Weak transcription	Psoas Muscle	Psoas
10	chr4:1342800-1379800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr4:1342800-1381200	Strong transcription	Fetal Intestine Small	intestine
12	chr4:1343400-1381200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr4:1344400-1364800	Weak transcription	Stomach Mucosa	stomach
14	chr4:1346000-1386600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr4:1346000-1389200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr4:1346600-1369200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr4:1346800-1363000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr4:1346800-1365200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr4:1347800-1362000	Weak transcription	Brain Substantia Nigra	brain
20	chr4:1349600-1364200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr4:1349800-1361000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr4:1350000-1364800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr4:1350000-1365000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:1351600-1361200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:1351800-1369400	Weak transcription	Colon Smooth Muscle	Colon
26	chr4:1352000-1360400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr4:1352000-1364800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:1352400-1369000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr4:1352600-1382000	Weak transcription	Fetal Brain Male	brain
30	chr4:1352800-1365000	Weak transcription	Fetal Lung	lung
31	chr4:1353000-1360000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr4:1353200-1360200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr4:1353200-1361200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr4:1353200-1361400	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr4:1353200-1361600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr4:1353200-1365400	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr4:1353200-1368800	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr4:1353400-1362400	Weak transcription	Liver	Liver
39	chr4:1353400-1369200	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr4:1353400-1382000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:1353600-1379600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr4:1353600-1382200	Weak transcription	Osteobl	bone
43	chr4:1353800-1364800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:1353800-1380000	Weak transcription	GM12878-XiMat	blood
45	chr4:1354000-1360200	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr4:1354200-1361400	Weak transcription	Colonic Mucosa	Colon
47	chr4:1354400-1359800	Weak transcription	Duodenum Mucosa	Duodenum
48	chr4:1354400-1365200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:1354600-1359800	Weak transcription	Fetal Intestine Large	intestine
50	chr4:1354800-1361600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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