| Tag | Content |
|---|
EnhancerAtlas ID | HS101-41473 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:129208830-129210600 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:129209472-129209484 | AAACAAACAAAC | - | 6.32 | | HES2 | MA0616.2 | chr7:129209328-129209338 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr7:129209328-129209338 | GGCACGTGCC | - | 6.02 | | Nr5a2 | MA0505.1 | chr7:129210127-129210142 | GCTGGCCTTGAACTC | - | 8.25 |
|
| | 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 |
| GH07I129569 | chr7 | 129209123 | 129210534 |
|
Enhancer Sequence | AGATTTAAAA AAACAGAAAA GGGGCTGGGT GTGGTGGCTC ACGCCTGTAA TCCCAGCACT 60
TTGGGAGGCT GAGGCAGGCA GATCATGAAG TCAGGAGATC AAGACCATCC TGGCTAACAC 120
GGTGAAACCC CGTCTCTACT AAAAATACAA AAACATTAGC CGGGCGTGGT GGTGAGCACC 180
TGTAGTCCCA GCCACTCGGG AGGCTGAGGC AAGAGAATGG CGTGAACCTG GGAGGCGGAG 240
CTTGCGGTGA GACGAGATTG CACCCCTGCA CTCCAGCCTG GGTGACAGAG CAAGACTCCG 300
TCTCAAAAAA AAAAGTCAGC ATCATTAGTC ACATGAAAGG CTCTTTAGGC CAGGCACAGT 360
GGCTCATATC TGTTATCTCA ACACTTTGGG AAGCTGAGGT AGGAGGATCA CTTGAACCCA 420
AGTGTTCAAG ACCAGCCTGG GCAACAGAGT GAGGCCTGTC TCTTAAAAAA AAAAAAAAAA 480
AGTGACATGC CTAATAGTGG CACGTGCCTG TAGTCCTAGA TACTCAGGAG GCTGAGGTGG 540
AAGGATCGCT TGAGCCCACG AAGTTGAAGC TACAGTGAGC CCTGATAGCA CCACTGCACT 600
CCAGCCTGGG TGACAGAGTG AGACCCTGGA TCAAAAAAAG AAAAACAAAC AAACAAAAAA 660
GAAGGTTGTT TAAAGACTAT GGGATTCATA AGTCCCCCCC AGCCATGTCG GCAAAAGCCA 720
AACATAGAGA AAAGGTTATC TTGAAAGGAT TTGTGCACAA GCCTCTTATC TAATGGAATG 780
AATCCCCATG ACATTCACAG GAAACCCACT AGGCTCTTGA GAATTTTATT CCAGCAGAAA 840
TACTGCCAGC TTGGACTGAA AGGGAGAGAG AGAGGATGAA ATGTAAGAAG GCTGTGGATC 900
CCCAAAATTC TACTGGCAAG AAACAGGCTG GTAAAACTAT TCAGCTGCAA ACACCAGCCA 960
TGTTTCATGA AAAAGGAATG ATGACTCAGA GGGCGAAGGT TTGAGCCCAG AGGGTGGGGT 1020
GGAGCCTTGA ACCACAGAGG ATCATTACCA GGTCTGGAAA ACTAATGTTT GCCCAGATAG 1080
ATTTTTTTTT TTTTTTTTTG AGACAGTCTC ACTCTGTCAC CCAGGCTGGA ATGCAATGGT 1140
GTGATCTCGG TTCACTGCAA CCTCCACTTC CCAGGCTCAA GGGATCCTCC CACCTCAGCC 1200
TCTTGAATAG CTGGGACTGC AGGCACACAC CACCATGCCC AGCTAATTTT TTTTTTTTGT 1260
ATTTTTGGTA GAGACGGGGT TTCACCATGT TGCCCGGGCT GGCCTTGAAC TCCTGACCTA 1320
AGTGATCTGC CCACCTTGGC CTCCCAAAGT GCTGGAATTA CAGGTGTGAA CACCACTACT 1380
CCTGGCCTGC CTGGATAGAT TTTGAAATTG TATGGGACTG ATGCTTCCTT TTTTCCTTCT 1440
GTTTTCTCCC TTTTTTGAAT GGGAATGTCT ACAATTGCTA TTTTATGGCT GTCTCAGCAT 1500
TGTATCTTGG GAACAGATAA CTTGTTTTCT ATTTTCAAAC ATCCACAGAT GGAGAGAAGT 1560
TTTGCCCCAA GAGGGACTGT ACCAACAACT CACCTATATT CAATTTAAAT GATACAGATG 1620
ATGAGATTTG GGACTTTAGA GCTGATGAGA CTTCACTGAC ATTTTGGACT TGAGTTGTTG 1680
CTTCAGTGGG TTGAGACATT ATGGGTGAAT ATATTTTTGC ACTTAGGACA GATGTGAATC 1740
TTTGGGAACC AGAGGGCAAA CTAAGTTTGT 1770
|
