| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00339 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:11972900-11974220 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr1:11973267-11973282 | AGTTAATGATTAATA | + | 6.4 | | HNF1A | MA0046.2 | chr1:11973267-11973282 | AGTTAATGATTAATA | - | 7.39 | | HNF1B | MA0153.2 | chr1:11973268-11973281 | GTTAATGATTAAT | - | 6.02 | | HNF1B | MA0153.2 | chr1:11973268-11973281 | GTTAATGATTAAT | + | 7.34 | | PAX5 | MA0014.3 | chr1:11972923-11972935 | GAGCGTGACCAT | + | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 11973466 | 11973675 | | chr1 | 11973200 | 11974088 |
|
Enhancer Sequence | GGAAGAGCAT GAAAGTGGAC AAGGAGCGTG ACCATGGAAG CACAGCACCA CAGGGAGGGG 60
TTTAGGCCTC CGGATGACTG CGGGCAGGCC TGGATAATAT CCAGCCTCCC ACAAGAAGCT 120
GGTGGAGCAG AGTGTTCCCT GACTCCTCCA AGGAAACGGA GACTCCCTTT CACGGTTTGC 180
TAAGTAACGG GTGCCTTCCC AGGCACTGGC ATTACCACTT GACCAAGGAG CCCTCAAGCG 240
GCCCTGATGC AGGTGTGACA GAGGGCTCAC CTCTTGCCTT CTTGGTCACT TCTCACAATG 300
TCCCTTCAGC CCCTGTCCCT ATACCCGCCG GTTATTCCTT GGTTATACAA CAAAGAGTAA 360
TATTAAAAGT TAATGATTAA TAATGTTTAT ACTAATGATT TATAATGTCC ATGATCATCT 420
CTATATCTAA TTTGTATTAT AACTATTCTC ATTCTAACTA TTTTGTTTAT TATACTGAAA 480
CAGTTTGTGC CTTCAGTCTC TTGCCTCGGC ACCTGGGTAA TCCTCCGTCC ACACTCGTCT 540
GTCTCTCCTG CAGGCTGCAT TCGCTGAGGT GTGTCTGTGT TGTTCCCCTT TGAGTTCCAG 600
TCAAAAAAGA TTCCTAGAGA GAATTCGCTC TCACGCCAGG GCTAAGCTCC TCCCACCAGG 660
TTCATGAGCC TGGAAGTAAG TGCCGTCCAC CAATGTCCTG CCTGCTCTTC AGAGGCTCCT 720
CAAGCCTTCC CTGCCCAGAG AGATTCCGGG ATGAAAAGGA AAAACGTCCC TGCCTGGCAG 780
AAATTGATGC TGCTTCTGGA AACGTAGGGC GGGTGGTTGT TTCCAAAATG TGTCTGCCAT 840
CACTTGAGCT AGTAGTGGGA GCATCTAGTT TTGGAGCTGG ACAGGCTTGG GAACGCATCC 900
CTGACTCCAC AAATTATGTG ACTTTGGCTT AATGACTTAT CATCTGGGAG CCTCACTTTC 960
CTCATCTGTA AAACAGGACT GACACTCACC TTGCAGGAAT ACTGGAGGTC TGTACTGCGC 1020
TGCCAACATC TATTCGCCCT CATCCGTGAC AAGAGTACCC ACAATTTCCT CTGGGAAGCT 1080
GCTCCTCTCT GATTAGTGTC TGTTCAGTGG TTGGAGGTTG ACCCTACCCC AGCTCTGAGA 1140
CGGCCTGGCC AGCCTATCCT AATTAGCATA TCCCTTTCAC CCTGGCCACA GTGATTGACT 1200
TAGGGCTGGG CTGTGCAGAG GTGAGCCTCA GCTTTTTGGG TAGGAACACC AGGACTTGGA 1260
TTCCAGTGGG TTTAATGCTA GGAGGGCATC AAGCTTGTGA TAACTGTGGC CATTTTTGTT 1320
|
