| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00097 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:1932270-1933710 |
Target genes | | Number: 26 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:1932376-1932397 | TCTTCCTCTCCCCCTTCCCTT | - | 6.29 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1933209 | 1933411 | | chr1 | 1933392 | 1933484 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I002001 | chr1 | 1933381 | 1933530 |
|
Enhancer Sequence | TCTCAGGTCC TGAGGCTTAG AGACAGCCCC GATGGCCACG GTGCCACTGT GTGGATGAAT 60
CTCTCGCACA ACCCCGAGGA GAAAAAGACA GAGGCCCGCC TGATGCTCTT CCTCTCCCCC 120
TTCCCTTCAC TGTCACAGTA GGTTCCCTGG GTAGGGCAGG TGGAGCAGGA TCCACAGTGG 180
CCCAGGCTGG GCTGTCGGAG CCTGGCTGGG TGAGGAGGGT GAGGGTATGT GGCTGAGGCT 240
CAGAGCTGTT TGCAGGTGCC TGGCTGGGTG AGGAGGGTGC CGGTGTGCGT GGCTGAGGCT 300
CAGAGCTGGA TGTCAGAGCC TGAGAAGAAA GAGGGCGGCC CCAGGTGTGG TCCAGCAGAG 360
GGTATCAGAG CCCAGGCAGG AGAAGAAGGT GTCCACCATG AGAGCCTCCC AGGCCAAGCC 420
TGGGAGTGAT GACATATTTG CATAGCTTCC AAATACCTCC TACAAAATGC TTGTGTTTTT 480
GTTTTGTTTT GTTTTTCATT TTGTTTTTTT TTTTTTGAGA CGGAGTCTCG CTCTGTCGCC 540
CAGGCTGGAG TGCAGTGGCG CAGGGTCGGC TCACTGCAAA CTCCGCCTCC TGGGTTCACG 600
CCATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTACA GGCAACCGCC ACCACACCTG 660
GCTAATTTTT GTATTTTTAG TAGAGACGGT TTCACCGTGT TAGCCAGGAT GGTCTCGATC 720
TACTGACCTC GTGATCCGCC CTCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC 780
CACTGCACCC GGCCAAAATG CTTGTTAATT ACGAAGGAAA AAAGAACTTC CCAGTGGAGA 840
TGTTGGCAGA TACCACCTTA ATCAAGAGCT CAAAGTGAAC ATCATCAGTA ACGTGACAAC 900
GTGACCACTG TGAGCCACTG ACTGGATGGA ATGAACAGGC CACGGTGTCA CCTCTGCGAC 960
TTTCCTGTCC GAGACGTGCA GTGGGAATCT AATCACGAGG ACACAGCAGA CGAAACCAAA 1020
TGGAGGGACT TTCTCCAAAG TAATTGGCCC ATGACCTTCA GAGGTGTCAG GGTCATGACA 1080
GCCAAAGCAA GGCCAAGGAA TGTTCTGGAC TGAAGGGGAA TAAAGAGGTA TGTGAGAATT 1140
CAGTGCAAAG TGACTCTAGG CTGGATCCTT CCACGCTGGG GCCCTGATGC AATCAACTGG 1200
CAAAGCGTGT TTGACAGGCT GAGGGGTAAA CACGGCAACA GGCCTGTGTC CTCTCCTGAC 1260
TCGGGCCATG TGTGGCTGTG TTGGAGAATG TCCTCGTTTG TGGAAAATAC ACTCTACAAG 1320
GGTGGGGGGC GACAGAGCAT CATGAAGGCA ACTTACTCTC AAATCCTTCA CGAGAAGTTT 1380
TTTTGTGCTG AGCTTGCAAC TTTTATACAA GTTTGGGATT GTTTCAAAAA ATGTTAAAGA 1440
|
