| Tag | Content |
|---|
EnhancerAtlas ID | HS101-22870 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:9466740-9467950 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DMRT3 | MA0610.1 | chr2:9467086-9467097 | TTTGATACATT | - | 6.02 | | FOXF2 | MA0030.1 | chr2:9466953-9466967 | ATTGTTTACTTTTA | - | 6.51 | | HOXA13 | MA0650.2 | chr2:9466867-9466878 | GTTTTATTGGC | - | 6.14 | | MEF2C | MA0497.1 | chr2:9467451-9467466 | AAGTTAAAAATAGCT | + | 6.12 | | Twist2 | MA0633.1 | chr2:9466911-9466921 | ACCATATGTT | + | 6.02 |
|
| | 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 |
| GH02I009326 | chr2 | 9467041 | 9467853 |
|
Enhancer Sequence | AGTAAACATC TTTATATGTC CCTATGTATA CATTCAAAAA AAATCGTATA AGTAGATCTT 60
TCGCTGCTGA TGCTTTATAA CCTATTTTCA CTCTCTAGTA TGTTGATGTC CATGTCAGAA 120
ATTTTGGGTT TTATTGGCTT AGTGGCCGCA CAGTATTTTC TGTATGGATG CACCATATGT 180
TAATTTCCCA CTCATTAGGT TTGGACTGTT GCCATTGTTT ACTTTTATAA ACAGGATAGC 240
AGTGTATCTT CTTTTCTGTT CATCTTTGTA AACTTTTGTG GTTATCTTCT TAGAATAAAT 300
TCCTGGGAGT AGAATTTCTA GGTCAAAATG TACATACGTT TAAAAATTTG ATACATTACC 360
AAATATTTAA TATCAAAAAG AAAGAGGGAA AGAAGGACCT ATAGGTGGTT GTTACAGGCA 420
GAAGGACAAT TTGTAGCTTA CAGTTTCACA GCAGCTTTCC ACCTCCTCCT TGGGCTGCAG 480
AGAGACCTCA GCCAGCAACT GAACTTGGGT ACCCCTACCC CACCCCCGCC CATCCTTTAC 540
AGCTGAGAGC CAGGGCATGA ATCAGCAGCT TTTCCAGGGG ACATTCCATT TCAGAGATCA 600
TCTTCTGACA GCGGAGGGGA TGGGGACTCA TGAAGTCCTT CTATTTCCTG ACACTGGTTT 660
TGTAGCTCCC TGAGGCTTTC TGATAGCTTC GTGGTCACTA ATGAATTCTC CAAGTTAAAA 720
ATAGCTTTAA TTCATTTCAA TTAAACTTTG TTTTTTTCCA ACAATCACAT TATTTTCCTT 780
GTAAGGGAAA TGTCTCAGGA CGAGAGACAT GATGCCAAGC ATCTCAGCTA CAATACGTTA 840
GCAGTTATTG TTCCTAAAGT AAGGGACCTT GGGCAGGAGT GTGTTTGAGA TGGTTAGAAA 900
TCCCATTTAT TTGAACCATC CATAGTCTTC CATGTAGCTA GAGTGAAGAT TTCTCCTAGC 960
AGGCCAGGAT AGACTGTCTT ATTATTAGGA GTTTTTGGCA CTTCAATATT TAATTATCTG 1020
ACTGTCAGAT AATTCATATG GCCCCAAAAT AAAGAAACGG TTACGGAATC CAGGCGATAC 1080
TAAGTGTCGA TCATGCACTC TACGCATTGT AAAAGATGCC AAAGAAGTAG AAGAAATCAT 1140
CTCAGTCCTC AGAAGCTCCT TTTAAACTCG TATTCTGCTT ACTTCCATGA CATTTCCTTT 1200
TCATTGTTCA 1210
|
