| Tag | Content |
|---|
EnhancerAtlas ID | HS093-22854 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr3:182977430-182978530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr3:182977471-182977489 | CTCTCCTTCCTTCCACCC | - | 6.24 | | EWSR1-FLI1 | MA0149.1 | chr3:182977467-182977485 | CCTCCTCTCCTTCCTTCC | - | 6.49 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23403 | chr3:182976883-182978398 | Colon_Crypt_1 | | SE_24158 | chr3:182977672-182978036 | Colon_Crypt_2 | | SE_24947 | chr3:182977300-182978461 | Colon_Crypt_3 | | SE_27019 | chr3:182977271-182978197 | Esophagus | | SE_27874 | chr3:182976750-182988749 | Fetal_Intestine | | SE_28762 | chr3:182976673-182987346 | Fetal_Intestine_Large | | SE_52684 | chr3:182976820-182978481 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I183259 | chr3 | 182977207 | 182978987 |
|
Enhancer Sequence | TGCTTAAAAC ATCCTCCCTG AGTCCGGTAC TTTTTTGCCT CCTCTCCTTC CTTCCACCCC 60
ACCTCTTTTT GTCACCCTCC TGCGACTTTG GATCTCCATC CTTGGAGTCC CTGAATCTTT 120
TTTGTGGTTG AAAGACTACA CCCAAAGGAC ACAGACTGAT GAGGTCACTT CTGCCCACTG 180
TCTAGTACTA GTGAGACCAA GAAGAAGAAG GAGGGAAAAC TGAAATGGAA GGTTTGAAAA 240
AGAGTGTGTT AGTGAAGGAA GTAAGAACAG TGCTAACAGA ATGCAGCAAA ACAGAAATGA 300
CTTCACACTT CTGGCAGTGA AGCAAATTCT CATCCATCTT GGGTTGCTTC TCTTGACCCT 360
GCCCACCTCC TCCCCTGCCC TCCCCTCCCG ATGAGAACTG CAGGAACACC TGTGCCCATG 420
CCAAGGAAAA AGGGCAGGTG AGGAACACAG GGATGGGGCT GGGACTCACA AGCTGCTCTA 480
AGCTGCCACA GGGTCTGGAA TTTGTTGACA TTACATGGTT AACTCGGTAT CTCGATGCCT 540
CAGTATCTTC TGCAAAATGT GGAGGGAGAT CCTTTCTTCC TCAAAGGTTG TTGTAAGGCT 600
TAAAGAGCTA CCACATTCGT AAGGCATTTG GAACAGGGCC TGGTATATAG TAGACATACC 660
CATGGTAGTA ACTGTTGCTA GACTGGGTAA AAGGAGAAGT TTCTTAAGTA GGCAAGAAAA 720
AAACTGACAA CAGTTATATT TAAAAGAGCA AGCAACCGTG TCAGCCCAAA CAAGTGTGTT 780
GCAAGAATGA GCACAGAGGG CCAAGCTCAG AAAAGCGAGT GTTTGACCTC TCTGAGACCT 840
CCTTTATATG TCAGCTTTTT TATTTGTTTC AAATTTTGCA TAATCAAACT GGTTACTGGG 900
AATTATTGAG TTCATATAAC TTCCCTAAAA TCTAAGAATA ATCTATAATC CCATGCCACC 960
AGTCCCGTTA ATAAAGACTT AGGGTCTGTC TTTACCCATT TGTTCATTTG AAATTCCCCG 1020
TCTTTACTTC CCCCATAACC AGGAAACAGA TCTACACCCA TGTTTAACTT ATAAAGAGAT 1080
ATAAGTGAGT TTACATAGGT 1100
|
