| Tag | Content |
|---|
EnhancerAtlas ID | HS101-02307 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:113210090-113211930 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:113211116-113211128 | GTTTGTTTGTTT | + | 6.32 | | IRF1 | MA0050.2 | chr1:113211486-113211507 | AGAGTGAAAGTGAAACAGGCA | - | 7.06 | | Nr2f6(var.2) | MA0728.1 | chr1:113211326-113211341 | TGAACTCCTGACCTC | - | 6.22 | | PRDM1 | MA0508.2 | chr1:113211489-113211499 | GTGAAAGTGA | - | 6.02 | | STAT1 | MA0137.3 | chr1:113211455-113211466 | TTTCTAGGAAA | + | 6.14 | | Stat4 | MA0518.1 | chr1:113211455-113211469 | TTTCTAGGAAATTA | + | 6 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I112667 | chr1 | 113210353 | 113212163 |
|
Enhancer Sequence | CATTTATATC ATTAGAGAAA CAACATTTTT AGGAGTATTC AATTAGAATG TTTTGTGGTT 60
TGGTGGTGGT GGTCTATTTG AGACAGGAAT TCACTCTGTT GCCTAGGCTG GAGTGCAAGG 120
AAGGACATGA TCACAGCTCA CTGCAGCCTT GAGCTCCCAG GCTCAAGCGA TCCTCCCACC 180
TCAGCCTCCC AAGTAGCTGG GACCACAGGT GCATGCCACC ATGCCCAGCT AATTTTTTTA 240
TTTTTGGTAG AGATGAGGTT TCTATGTTGC TGAGGCTGGT CTCAAACTCC TAGACTGAAG 300
TGATCCCCCT GCCTCAGCCT CCCAAAGTAC TGGGATTACA GGTGTGAGCC ACCATGCCTG 360
GCCACTATTG TGTTCTATAC CTTGAAAGAA GAGACATGAT TTGTTCTTGC ATTTCTTTGA 420
TAGTCTCATT ACTTCTTTAA GTTATTAGAA GTTATTGAGT ACCCCCAAAG AGTTTTTGTT 480
TATGTGTTAG ATCTATCAAT GTTTACCTCA CTAAAAATTA AAGCTGAGAA GTGTGGGCCG 540
GGAGTGGTGG CTCACACCTG TAATCCCAGC ACTTTGGGAG GTCGAGGCAG GTGAAAGCTT 600
GAGCTCAGGA GTTCAAGACC AGCCTGAGCA ACACGGTGAA ACCCTGTCTC TACAAAAAAA 660
ATATAAAAAT CAGCTGAGTT CCTGTAGTCC CAGCTACTTG GGAGGCTGTG GTGGGAGGAT 720
CACCTCAGCC CAGGAAGGTT GAGGCTGCAG TGAGCCAAGA TCGTGCCACT GCACTTCAGC 780
CTGGGTGACA GAATGAAACC CTGTCTCAAA AAGAAAGAAA GAAAGAAAAC TAAGAAGTGT 840
TAAAACTATT CGTTAATTAA AAATAATGAT AACAAACCCA TTACTTGTTA ATAAGTAACA 900
TCTTTGTGAA TATATTTTCC AAATCAAAAG AAAAAAATAG TGGGAAGAAT GGCATTAGTC 960
TGTGTCTTCA CAAATTGTGT ATTAAAAGAT GGCGGACTTT ATTGTGATAT TAGTTGTTTT 1020
TTGCTTGTTT GTTTGTTTTT TTGAGATGAA GTTTCGCTCT TGTTGCCCAG GCTGGAGCAC 1080
TGTCTTGGCT CACTGCAACC ACCACCTCCC AGGTTCAAGT GATTCTCCTG CCTCAGGCTC 1140
CCGAGTAGCT GGGATTACAG GTGTCTGCCA CCATGCCCAG CTAATTTTTG TATTTTTAGT 1200
AGAGACAGGG TTTCACCATG TTGACCAGGC TTGTCTTGAA CTCCTGACCT CACCTGCCTC 1260
GGCCTCCCAA AGTGCTGGGA TTACAGACAT GAGCCACTGT ACCTGGCCTC TGCTTCATAC 1320
CTTTCATTAT CCCTGAAAGT GATAAAGTCA TCACACATCA TGTAGTTTCT AGGAAATTAC 1380
ATCATACACA CATTACAGAG TGAAAGTGAA ACAGGCAAAT AACTTTGTGT TAGTATTATT 1440
ATGAAAGTAG AAAATAGTTT TGACCTCATA GTCTGTCTTA GGACTGCAGC TCTAGATATT 1500
AAATCCTACC CTCTTCCCTT TAATTCTGTT GTACTTAATG GTAACAGGAA GAGGGAGATT 1560
CATTTCATTT TAGACTTGAA CCACGTGGTA CAAAATGTGA TTGGCTAGTT TAACATCATA 1620
AGTGGCAAAT AAAGGCATAT GTGAGCTTAT GTATATGACT GATGTGTCCA AGGGCATTGT 1680
TCATACCATT TTAAACCAGA AATATTTTCA AGGCATCAAG GTTTCAAGAC TTGATGATGT 1740
CTTTTGGGCG TACTGTGGTA GAGTGGAAAC AGCATGGGTT TTTTTGGTGA AGACCTAATT 1800
TCAGATCCCA TCTTTATCAT TCAAAAGCTG TATAATTCTG 1840
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