| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00147 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:7551020-7552230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr1:7551354-7551370 | GCTTGTTTACTTAAGG | - | 7.43 | | FOXP2 | MA0593.1 | chr1:7551887-7551898 | TTTGTTTACTT | - | 6.62 | | HSF1 | MA0486.2 | chr1:7551519-7551532 | TTCCGGAATGTTC | + | 6.07 |
|
| | 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 |
| GH01I007490 | chr1 | 7550829 | 7552540 |
|
Enhancer Sequence | CTTCCCCACT CCAGCTCCGA TCCATTGACT CAGCTTTTGT TCTGTGAATG TCATTTTCTT 60
TGAATTTGTG TGAGTTTTGT TGTTTGCAAA TAACCTAATG AAACTCCTTC TGTTCCCTTC 120
CAAAACAAAA AGGAGGCTCT AGCATGGTCT ACCTCCACAT CTGAACTCCT CCAAGCTTTT 180
CTGATGGTGT TTGGGCTGTA CAGCACCCTG AGAGACCACC CCCGGCCTCC ATGTACCCCC 240
TGCCATCACC TGAGCCGCAC TCACCAAGGC AGAGCCGGGA GGACTCCACC CACCCTCTTT 300
CCTGTTCATA AGGTTTCTCA AGGAGCCTCT TGATGCTTGT TTACTTAAGG ACGGGCACGG 360
GTGAACTCTC ACCCCCACCT GGTGATTTCA CAAACACAAA CCATAGAGGG GAAGGCTATT 420
TCTCTCACTT TCTGGAAAAG GCCAAAACTA ACCCTGAATC CCCCCGCCCA TGTTTAGAGT 480
AGACACAGAG GGAAGATGGT TCCGGAATGT TCTGCGTGTA CTGCCGATTG TCCAATTGCT 540
TAAAACAGGG CTTGGCGTGC ATTGTTTTGG TCATTAGTTA ACCAATCTGG GCGGGGAAAA 600
AGGCAGAGCG TTAAATAATT ACAAGCACTT CGGTGATTTT TTTTTCTACT GACTAAGGTT 660
AAAATGAATA GTGTTGATCC GTTGCCCAGG CAGCAGGCTT GTTAAAGGAA ATGGTATTTA 720
AAATGATTTT TGAGCCAAAG CAATTTGGCT GCTTCAAGGC ATCCTTTATC TTTTGCTTTC 780
AAGAGGATAA TAATGTTTAA AAACGAAGTC ACTCATACCA TTTCCTGTCG CGAAGCCAGC 840
TCAGTGATGG GCAGAGCTTC CTCTGGGTTT GTTTACTTGC TCCATGATGG AAAATGCAAA 900
CTTAATGGGC TCCCTTCTGC CGAGGCTTTG GTGTTCCGAC GAAACAAAGA CCCATGCTGC 960
TGCCGAATCT GTGTCCACAG CTCTGGCCAG CTCACCCTGG AAGTCTTGAT TGCCACATTG 1020
TGGATGTCAG AATGTCACCT GCTTGGTTAG AGCTTCTAAA CAGGAGGCTC AAGGCCACTC 1080
CCTGGCTCTA GGGTGGAGTC GAGGAAACCT GTCTAGGATG GGACACGCTC CCACTAGGCT 1140
CAGGGTGCCC TCCCGTCCAA GAGCATGATG GTCACCCCAG CTGGGAAGTT GCTAAGCAAG 1200
TCCTCCTTGG 1210
|
