| Tag | Content |
|---|
EnhancerAtlas ID | HS101-37708 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr6:47401770-47403140 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr6:47402415-47402431 | ATTTGTTTACATAATG | - | 7.65 | | FOXP2 | MA0593.1 | chr6:47402416-47402427 | TTTGTTTACAT | - | 6.14 | | LMX1B | MA0703.2 | chr6:47402432-47402443 | TTAATTAAAAT | - | 6.62 | | MSC | MA0665.1 | chr6:47402533-47402543 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr6:47402533-47402543 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr6:47402533-47402543 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr6:47402533-47402543 | AACAGCTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 47402288 | 47402684 | | chr6 | 47402519 | 47402611 |
|
Enhancer Sequence | TGTGGTGTCA CATACTTATA GTTTTAGCTA CTTGGGAGTC TGAGGCAGGA GGCTGCTTAA 60
GCCCAGAAGT TAGGGGTTTC AGTGAGCTAT GATTGCACCA CTGTACTTCA GCCTGGGCAA 120
CAGAGTGAGG CCCAGTCTCA AAAAAGTAAA TAAGTAAATA CGTATATGTT AAACATCTTA 180
TTTTACCTCA CACATATAAA ACATGAAACA TTGATTTGCT AGACTTTTAA CAGAGGGCCA 240
AGACTATTTA ATTTATAAAG GGACTGCTAA ATGGAGTTCT GAGTCTTCTT TCTAGAATAC 300
AGATACCCAT GATGTGATTT TCTGGATATG ATTTTTATAA AGTGGAGTAA GAACTTATAC 360
AGATTTGTGG AACAAGTACA GAATCCATCT AGATGTCAGT GATTTTCCCC TAATCTTTTA 420
CTGTTATTTA TAGATTTCTT AAGCTTTTGT TTGGGTTCTG GGTTTTTTTT TTTTTTTTTT 480
TTTTGGCAAC TCACCTCTGT AGAGATCAGA GATCCTCCAA AGTATTCAAT TTACTACAGT 540
AAACTTTGAC CACGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTTGGTT CATAACTTTT 600
TATATTATGA AACTTTAACT ATTTTTGTTT CTGCACTCAT GTTATATTTG TTTACATAAT 660
GTTTAATTAA AATCTATAAG GGTTTGGGTT TAGAGAAGGG TAAGCACACT CCTCCCAGTC 720
TTTCTCACTG AATGCAGCTG TAAAATCTGG ACAGAATGCA AGCAACAGCT GTTTATCTGA 780
AAAGTAAATA ATAGCAGGCA GATTAAGGCC AGAGGAAAGT CCAGAATGTG AAGTACCACT 840
GACTGAAGTG GCATTGAGTT TATCAGCTTT TTTCCTCCAG TCCTCCCAAG GCTTAGCCCC 900
ACAGGTGGGC ACAGCTATGG AAGTTTACAG CAGAGTCGTA TAAACAGAGC TCCACCTTTC 960
AGGCCACAAA ACCAAAAAAG GGGAGTCCAG GAAACTGGAA AGTACTGGGA AAGAGAAGTA 1020
CTTGGAAAAG TAACCCCATA AAGTTATTTA TGAATGCCAA GCTCACTCTA AAGTTGCACA 1080
TACATAGATC TGAACTTAAT CAGCATTTAT ATGACTTTTA TAAGACTTTG AGAACTTAGC 1140
AGATAAATTC TTGGCCCCCA TATCATATTG GCCACTGGGT GGTGAACATG TGGGACAGAT 1200
CCCAACAGCA CAGCAAAGGC ATTGAACACC GAATTGGTGT TGGAACCACA ATCCACTGAA 1260
AGTACATTGG AAATTGTGAC CTGAACCTAA CTAGATTATT TGTCTGCGAA AACAAAAATA 1320
GCAGCATTCT CCATAGGATT TAAACAAGGC CCAGCATCTC ATAACATAAT 1370
|
