| Tag | Content |
|---|
EnhancerAtlas ID | HS073-11705 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr5:134211620-134213350 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr5:134213108-134213129 | TTTATCTTTCAGTTTCACTTG | + | 7.07 |
|
| | 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 |
| GH05I134876 | chr5 | 134212368 | 134213329 |
|
Enhancer Sequence | GAGTGCTGGG ATTACAGGCT TGAGCCACCG TGCCTGGCCT TAGTAATTTT TAAATGCATA 60
TGCAGTAGAT GTTATCATGC TCATTTTATA GAAGTAACTT AAGACTCAGA GCCAATAAGT 120
CCTTTGACAA GGTCATACAG CCAGAAGTTG AGGAGCCTTG ATTCAAGCCC ATGTCTGCCT 180
GACTTCAGAG CCCAACCTCT GCATTTTCAC TATACTTAAC TGCTAGCCTC ACAGAGGGGA 240
TGGCATGGGT TGGATATCTT CTGTTTCAGC CCCTCCACCG TGCTCTGTGC CCTGTGTGGC 300
TGTCCTGTGT GGAATAAATA CCAGCTGTCC TACCGTCTTG CTTCCATTGT GTTGGAATGA 360
GGGGAGAGTG AGGTCAGGGT ATTGATTCTC TCCGCTCCCT CCCTGAGAAG TTATTGAAGG 420
CTGGCTTTGC CCCCGGTGGA AAGCATTGAA TTCTAGAAAG CTGCCCTCTG TGTTACCCTT 480
GATGTTTCAA GGTTCTGTGA CTACTTCTCT CTCCAGACTC TTAAGGTCTA TGAGTGGTAA 540
CTGGCTCCTC CTCTACTGTT ACTGGCCTTG GAATTCCTTA CCATTGCTTT TCATTTCTCT 600
GCACCCAGCC TACACATTAG TGGTCCCTTC ATTAAACTCT CCTCAACTTG CCCAAGTTAA 660
ATGTGCTGTT TCCTGGCAGA ACCCTGGCTG ATTCAGGGTT CAGCTTGGGT CTTTGGTCAT 720
CATGGCCAGG CCATGAATGG GGTGAAGACA GAAGAAACTT CACCAGCTGA TTTCTTCTCA 780
GAGTAGCTGA AAATCTGAGG TGTTTTTTTT TTTTTTTTTT CTGCAGAGGA TGCCACTGGC 840
AGATTATGCT GGCCTCAGGT GCTGAGGCCC TGAGAGACTA AGCAACCTGG AGGTAGCAAT 900
GCTATCCAGG TGTCTAGGAA TGGAAGCAAA CTCCTGGCTT CAATACCCCT ATGCCACTCT 960
TCCCTAGGCA GTCAGCTAGC AAATTCTTAC TGAGCACTCA TCATATGCTA AACACTGTGC 1020
TGAGCACTGG GGATCCAGTG GTGAGTTAGA GCAGCAGGCC TTTGGGGAAG GCAGCCACTA 1080
AATAACTACA AATTACTAAG AAAATTGCAA GACTGAGAAA TGCATCAAGG AGAGTCCCAG 1140
GGCGTTTTTG GGAACTGTAA TGGGAGACCT CCCACCCTGG TCTGAGGGTC AGGGAATGTG 1200
TCCTTACAGA GGTGACATTT AGGGTGAGAT CTGAATGAGG AGGATGAAGG ATTTGGCAGG 1260
AGGAAGCTTC CCAGCAGAGA AACAGCCCTC AGGAAGGCTC TAAGGCAGGT GGGGATAGGA 1320
GGAGTGTAAA TGATCAGGGA CTAGAGGGAT CTGATGGCCA CAGGTGAGAG TGCAGACAGA 1380
GGCCACATTG GGGCCTGGTA GCTCTGCTAC AGAATGCAGA TGCATTCACA GGGTAGGGGA 1440
AGCCACTGAA AGAGTTTTAG CAGGGGAGTG ACATGATCAG ATATGCCTTT TATCTTTCAG 1500
TTTCACTTGT ATTGCTGTGA AGGTCAGGGT CTGGAGGGGG GATAGCAGGC TGACCAGGGA 1560
GACCAGTTTA GGTGGCTACA GTAGTTGCCC AGACAAGAAT TGGCTGTGGC CTTTGCTGAG 1620
AAGTGTTAGT TGGGATGGGG AAAGTAGATG GATTGTGAAT GTGTTTAGCA GGTGAAATTT 1680
TTTTTTTTCT TTTTGAGAAG GAGTCTTGCT CTTGTCACCC AGGCTGGAGT 1730
|
