Tag | Content |
---|
EnhancerAtlas ID | HS048-22449 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:239311970-239313500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr2:239312561-239312573 | TACCCGGAAGTG | + | 6.37 | ELF1 | MA0473.2 | chr2:239312561-239312573 | TACCCGGAAGTG | + | 6.62 | ELF3 | MA0640.1 | chr2:239312561-239312574 | TACCCGGAAGTGA | + | 7.04 | ELF4 | MA0641.1 | chr2:239312561-239312573 | TACCCGGAAGTG | + | 6.74 | ELF5 | MA0136.2 | chr2:239312562-239312573 | ACCCGGAAGTG | + | 6.32 | ZBTB7A | MA0750.2 | chr2:239312562-239312575 | ACCCGGAAGTGAG | + | 6.15 |
|
| 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 |
GH02I238404 | chr2 | 239313259 | 239315313 |
|
Enhancer Sequence | TTGTGGATAG TGCTATGTGT AAGTTTTTAA AGAAAATTAT CCTTACTGTC AATCATGTAT 60 CAATATCACC CTTAGTCGTG CCAGGTATTC ATGTTGGCAT AACTAATTCA TATTCCTAAA 120 GTATTCATTT CTTCTTATTT AAAGGACTTT TAATGGAAGA GGTAATATAT TAGCATGGAT 180 CCACAATCAC GGTTAGCTGA AAGGGTCCTC TGTGAGAGGT CCCCTCCCGT GGTCCCTGTC 240 TGCCTTGCTT CTCCTTGCCC CTGTAGGCAG CCATTTGCAT TAGACCCTTG TACAAGCAGA 300 TAAGAATATT TACTTTTATA CCCCTGCAAC ATACAGTTTC ACAAAAGGTC ATAGTCTATA 360 CCCTGTTCTG AACCTTGGCT TTTCGGATTT ATGCAGTCTG GGGACCTCAG AGTGTCCACC 420 CTAGACACCG TCCTCACTTC TCTCCAGGCT GCGTGGATCT CCCCCTGCGG CTGCCTGGCT 480 TCTCCTGCTG GCTCCCTGGT GCTCAGTCGC GTGGTTTCTA GTCTTCCGCC ATTAAAAGCA 540 ATGCCGCCGC GAATAGCTTT GTTCTCCCAT CATTTCTTCT GTGTGGAGAG ATACCCGGAA 600 GTGAGACTGC AGGGTCAAAG CACAGTGTGT CGCCATATTG GTGGGTGTTG CCAGATGCTG 660 TTTGTGGGAT GGTTCCATGT TCCTGCACCA GAAAATATGT GGAAGTGTCT TTTCCCTGCA 720 GCCTTCCAGC GGCGGATGGC CACACGTAGA CATTTCCACT GCTCAGGCGA GAAAGAGGAT 780 CTCAGCATGT TTTCATTTAC ACTTTCGCAT TTTGACTGAG TTGTAGCCTC TCTTGATGTG 840 TTTAAGGGTC ATTTGCTTGT TTGCTTTTCT GTTCTGTGAG CTGACTGTTC AGCTGCTCAT 900 TTGCCCTTTG TTCTGTTGGA CTCTTGGTTT TCCCTCCTGG ATTTCTAGAA GCACTTCGTG 960 TTTTGAGTTC ATATTATTCC CAGATTGCCT TTTGACTGTG CTATAGCTTC CTTGCCCCAG 1020 TGCGATGCTG GACAAATACG AAGGACAGTC CTTGTGATTT TATAATTGGT CCGATGCTGC 1080 CAGGAACGAT GGCGACGGCT GTTTTCTCGT GTTAAAAACA GACTCTTCTG ATCCTGGTTA 1140 CAGAGAACCT CTAGCAGGAA TGGATGTTGA ATTGTTCTTG TGATCGCATT TTGTCTCCTT 1200 TGGCTTAGTA ATGTGCTATT CTCGATTACC CAACATGAAA ATATCCTGCG TTCATAGATG 1260 AAGTCTTGCG TGCTCAGTCG GGCTGTTCCT CCCTCATGCT GAGTAGTTCT GCCGCACATG 1320 CGTGAATCCA CTGTTTCTTG CTGCCCGGTG CTTGTCAGCC GGCAGGGGGG TTGAGGGCAT 1380 TACTCTGTTG TTTGATTAAC CCCAGTCTTA GGTAGACACC GTGTCCCTGG GTCTTGGCTG 1440 TAGCTGGGTT GGGGGCATAC TCTGTTGCTT GATTAACCCC AGTCTTAGGT GGACACCGTG 1500 TCCCTGGGTC TTGGCTGTAG CTCTGGAACC 1530
|