| Tag | Content |
|---|
EnhancerAtlas ID | HS101-37393 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr6:36923540-36924650 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr6:36924085-36924096 | TGTGACTCATT | + | 6.62 |
|
| | 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 |
| GH06I036956 | chr6 | 36923777 | 36923977 |
|
Enhancer Sequence | GACAGAAGCC AGATTTAGGG TTGGTTACTT CTGTCAGGAA GAGCTATTTA TGGTAGGGTG 60
AGAGGCGGGC TGTCTATATG CAGAATTAAA GGAGATAAAG TGAGAAATTC ACCCACTTCC 120
TGCCCTCCCT GAGGGCTGAA CTAGCTTGTC CCCTCCAGCC ACCCTCAGGT GACTGGGGAG 180
GTTGCTGGGC AGTGTTCAGG GACCCCTGGA GCTGGTGCCT GAGAGAACAG ATGCACCTTG 240
GGGAACATAA CAGTGAGCCT GGGGCCCCAA ACCTAAGTTC TAACCTCAGC CTAATGTGAT 300
CTGGCTGAAG TAACTCTGGG TGGACCCCTT TCCCTTCAAA GGCCTCTGTT TCCAGATGGA 360
AACATGGGGC TGGCGATCCC TGCCCTGGGC GTCAGACAGG ATGACACGTA AGAAAGATCT 420
AGGAAGAGCT CTGCACACAC CCAGCACTGC CGTTCACAGC TGTGCCAGCC TGCACATCGA 480
GGAAAGGTGG ACAACAAACC AGGCGTCACA GATGCAGCTC TGCCAACAGC TCCCTGATTG 540
AGGCCTGTGA CTCATTGTTG GACTTCAGTT TCCCCACCTG TAGATCCCTG ATGCCCTACA 600
GTCTTGCTGG CTGAGACTGG GGGCCACACA GGCTGGGAGC TGCTTCTCAG ACAGAGGTGC 660
GCCTTGGAGT GGGGCAACAT TCTGGGAGGC AGTTGGGATA CTGAGGGGAT ATGCTGCTGC 720
CTAATGGGGA GTGACATGAG GAGGAGGAGA TGAGGCTGGG GCTGGGATGC CAGGAAACAT 780
TCAGGACAAG ACTCAGGTTC AACCTCAGCA GTGGTGAGGG CAGGGACTCT GCAGCCAAAT 840
GGCCTGGGTT CAAATCTTAG CTTTGTTACT TATTAGCTTT GTGACCTTGG CCAAATTAAA 900
CTCTCTGTGC CTCAGTCTCC TCATCTGTAA AATGGGGATG ATAACAGTGG GATAATTCCC 960
TTGTAGCTAC AGTGGTTGTA GGGTTAAGTG AGTGAATATG TGTAAAGCAC TCAGAAGAAT 1020
GCCTGGCACA CAGTAAGTGC TCAGTAAGTG TCTGATTAAC ACAAAAGAGG GAATGGATCC 1080
AGGGTGAGGC AGGTGGGGGT TATCATGAAC 1110
|
