| Tag | Content |
|---|
EnhancerAtlas ID | HS048-20741 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:85401970-85403470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | + | 6.49 | | Ar | MA0007.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | - | 7.04 | | NR3C1 | MA0113.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | - | 6.06 | | SOX10 | MA0442.2 | chr2:85403018-85403029 | GTCTTTGTTTT | - | 6.14 | | Twist2 | MA0633.1 | chr2:85403394-85403404 | 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 |
| GH02I085174 | chr2 | 85401720 | 85403770 |
|
Enhancer Sequence | TCACTGCAGG TCCCTGCCCG ACCCTACCTT TCTTCCTCCG GACCTCATAT TAGACCAGCT 60
CCTCAGGCCT TTTTGGACAT GACCGTCTCA AAGTGTTACT ATGTTTAAGT GTGTGGTTTT 120
TTGTTTATGT GTGTGGTTTT GTGTCTTTGA TATCGTTGAT TTGCCTTATG GCCTCAACCA 180
AACCCTCACT GTAACATGGC ACAGGCAGCG CCATGTGACA TCCTTGTCCC TGGCCCGCCC 240
GGCGCAGCTC ACAGTGGGCT CTCTGTGAAT GCTGGCTGGC TGAGTGTCTG GGAGTTGTGA 300
GCCCTTTGCC ATGTAACTGG AGAGGGTGGA AGTGTGAATG GAGACACCTG CTCAGTTGTA 360
CAATGCTCTT TGGACAGGGG ATCAGGTTTA AATCAGTTTG AAGCCTGCTT TACCACCCCC 420
TGCCCCCACA ATTGTTATTT CCTGAAAGCA TATGGTTGGC TGAGCTAGCT GAAAAATTAC 480
CCGAATTTTG ATAAAAATTT GAACCATGGA TTTCCTTTCT GACCATGCCT AGCTGTGTAA 540
ATTCCACAGG ATAGTAACAG GTGCCTGGCC ACCATCCAGC AAGACCCCTG ATAACGTCCA 600
TGCAGTGGGG AGCCACGGGG GCAAGTGCTT CCCCTCCCTC CTGGTCATAG GCTTGAGCAT 660
GGGTAGCCAG GATGGGGGGT GGGTGCAACT TGAGATAAGC AAATCGACAA CAATGAGGTA 720
CACCCTGTTC TTTGTCCTCT TGTCAACTTG TGATTTCCCG ATGGATCAGG TAATCCCCAG 780
TAGCAGATAA CTCAGTTGAA TTTTTTCACT GTCGCTGTTA TCTGTATTCA TTGTCTGCCT 840
AAATAGTAGT GAACAGAGAA AAAAAGAACA TTAAAATAGG AAGCTGGGAA TGACAGGAAG 900
AGGGACTGTA GGCCTGGTAA ACAAAAGTTG GCTGTAACAT GAGCCAGGAT ATGGAAGCGT 960
GACCAATACT TTGGACTCTC TCAATGCTGG CCCTCTGCGG TTCATGGCTC TCCTCCCTTT 1020
CTCGCTGTCA CCAGCCACGT TTAGGTCAGT CTTTGTTTTT GGCTGTTGTT CCTGAAGACG 1080
CATTTATCAG GTGGATCTCT TAAAATCAGG GTTAGGGATT GGAAGTCTAG CTGGGACAAT 1140
TCCTGTGAAG ACAGACTTCC TTCTGATGAA ATATTTACTA GCTTTTGTAG GAAGCCATCT 1200
CCTCCTCTTT GCTGTGATAA GAGGTACTCC CCACCTTTCT GTCTCATGGC AAGGGTGGAA 1260
ACTGATGATA TTTGTAGGGC ATACTGGGGT GAGCCAACAG GCTGGAGGCA GCCAACCCTG 1320
GGCATGCAAA GAAGCACCGT TTGGAAGCTC TGGTGTAGCT CTCGTGCAGC AGCAGTCCAG 1380
GCCCTGGGAC ATCTGAGTTT GAGGCTTCAG TCCTCCGCTG ACTGACCATA TGTTTACACT 1440
GCAGCCTGTT GTGGTATGAA ATGAGATCTG GAAGCACCTG AGCTCCCCAG TGTCTGCAGG 1500
|
