| Tag | Content |
|---|
EnhancerAtlas ID | HS048-23875 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr21:44140980-44142160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr21:44141299-44141317 | GGAAGAGAGGAGGGCAGG | + | 6.18 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23630 | chr21:44140970-44142161 | Colon_Crypt_1 | | SE_24305 | chr21:44141090-44141627 | Colon_Crypt_2 | | SE_24305 | chr21:44141669-44142090 | Colon_Crypt_2 | | SE_50726 | chr21:44139933-44142207 | Sigmoid_Colon | | SE_52828 | chr21:44140503-44142176 | Small_Intestine | | SE_57310 | chr21:44140546-44142156 | VACO_400 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 44141142 | 44141960 | | chr21 | 44141013 | 44142053 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH21I042718 | chr21 | 44139106 | 44145483 |
|
Enhancer Sequence | GGTGCATGTC TGTTAACCCA GCTGCTCGGG AGGCTGAGGC AGGAGAATTG CTTGAACCCG 60
GGAGGCGGAG GTTGCAGTGA GCTGAGATTT CGCCATTGCA TTCCAGCCTG GGTAACAAGA 120
GCGAAACTCC GTCTCAAAAA AAAAAAGAAG GATAGAGCTA ACATGCATGA ACCACCTAGA 180
ACAGCACCCA GAGCATAGTA ACAGCTCCTT GCAGATGTTA CAGTACCTTG ATCTATACAA 240
CAGTAAAGGG AAATGCATGC TAGCTGCCCC AGATGCTGCC AGCTTCACAG GCATTTTTCT 300
GCCTGCAAAC TAATCCTAAG GAAGAGAGGA GGGCAGGGGG AGAAATTGCA CCCAGTCAAA 360
TGTAAACGAT ACAAAATGTG AAATTCCCCT CTCTGAAAAT GAAAGGGAAA AAACTCGATT 420
CAATGCCTGC CCCTGAGGTG AACCTGAAAT GACAAGGCAG ACACTCTCTA GAACTTCACG 480
TTTGGCCACC AGGGTCTTCG GTTGATTTTC CTTTCTTCGT CATATCTGAG TGGCTGAAAC 540
GCCAGTGATC TGGGATAGTC CTTTGGCTGC TGATAGACTT ATGCAATCCC TTGGCAGGCA 600
GGACAGGCCA GAGGAAGGGC TCCTGTGCCT TTAAGGTCAC TGTTAATCAT GTAACTTTAT 660
TGTGTTCCTG GGCTATAAAG GAAATGTCGT CCTTGATCTG AATGTCTGTT TTATGATGTC 720
CATAAACAGT GAATTGCCAG TGACTGTACC CTGAGTGAGA ACATCCTCAG CCAGTTGAAT 780
AGTTCAAGGG CAGTTGCAGG GGTCAGGAGA GAGCAAAAGT GGGACAGAAG ATGAGTTTGC 840
TTCCCAGGAA GAGAGACAGT GCCACCCCAC CCCTCGCTGA CAGGGAAGCC TTCCAGCCCT 900
TCCTCCAAAG AGCCTTGGCT CTCAGGGGTT GGAGGTTGGA CAAGAGCAGA AATAAAGGCA 960
CCCTGCTCCC ACCCCCCACA ATCTTCCGGA CGTCTAGAGT GCTTATCTCT TTGGGGGCAA 1020
GTAATGTGAA TTATTTTCCC TAATGCAAAA ATAAAAAATA AGAGACCCCT TTTACCCTTT 1080
TCTGAAAGGA TAGCAGAGGT ATTTTTCTTT TCTTTTTTTT TTTTGAGATG GAATCTTGCT 1140
CTGTCACCAG GCTGGAGTGC AGTGGCACAA TCTCAGCTCA 1180
|
