| Tag | Content |
|---|
EnhancerAtlas ID | HS051-12133 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:56455910-56457200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr17:56456594-56456607 | TTCTAGAATTTTC | + | 6.71 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23473 | chr17:56456264-56457113 | Colon_Crypt_1 | | SE_28098 | chr17:56451905-56456269 | Fetal_Intestine | | SE_28098 | chr17:56456380-56462635 | Fetal_Intestine | | SE_28995 | chr17:56456285-56462192 | Fetal_Intestine_Large | | SE_34462 | chr17:56453810-56457073 | HCT-116 | | SE_50030 | chr17:56455820-56460841 | RPMI-8402 | | SE_56729 | chr17:56455684-56457124 | VACO_400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I058374 | chr17 | 56452143 | 56462492 |
|
Enhancer Sequence | TTTAAAAATT ATTTTACCAG AAAAGTGTAT TCCTGCTTCA TCGTATAATT TTTTAAGCTA 60
CAAAAGTAAA TAATGTTGGT GGGGAGGGAG AAGCATAACC TCGGGCCATC TGATGGGAGT 120
GCACACTAGC AGGGGATGGA TGAAGAGGCC TCCATGATTT CTCACTTGAT TCAGGAAACC 180
TCCTTGGGGG AACAGGGGTG CTGGTGAGCG AAAGAGCTGA CAAGATAGAA CTGAAATGAT 240
GTTCCAGAAT CTAATAGGAA GCAGGGTGGC AAAAACTGAG GGAAAAACTG AGCTCACTGA 300
AACTCCAGTC GGGGGCTCTG CATATCATAG GCCCTTAGTG TTTGGTGAAA GAATGAATAA 360
AACTTGATTT GAATCCAGTT GCCACGTAGT TTATAGAAGA GATGTAAATT GCTAACAGCT 420
GAGCCTGGTT CACACCCATA ATGGACCTTC AAAATTTGTC TTTTACAGCT GAAGAAAGCA 480
AGACTCAAGT TACAGATTGC CCACCTAGTT AAAGTTAGTC AACCTAGTCA ACACCCAGTT 540
AAAGGAGGTT GAGGTCCCCT AAATTCAACC CCACACTGCC TCCGGGTATG CACGCTGGGG 600
AGGCTTTTCT GTGGCATGGT AAGCATTAGG TGAGTACTGT AATATAATGC CTGGGATCAC 660
AGTGGAAGGC TTCAGGGTCC CCATTTCTAG AATTTTCAAA CTTGAATCAT TCTTAACAAG 720
ACAGAAGCAG GATCTGTCTG CTCCTTGTGC TCTGCCTCCC AGCCTCGGCT TCCTTCCTCT 780
CCTCTACGGT TTATCTCATC TCCTCTCCTA GCCACAACAA AGGCAGCCAG ACCCAGACGC 840
TGCTCAGAGA CACTTTCCCA GTGAAAAGTC CCTGTTGCTT TAGGATGAGA AAGGTGTGTC 900
CTGAAATTAG AGGTCACAGA AGCTCAGACC CAAGTAATGG TCATTCAGCC AGACTGCCAT 960
TTTCCTTACT CCTTCACCCC ACATTACAGA CGCCATTCTT CAATTTCCAA ATTCACCTAT 1020
CCTCATTTCA GACTGTGCTG GAGCTCCATG ATGCAACTAG GCTTCTTTAC ATGAAAACGG 1080
CCCCCATGGT GGGGTTCTCC TGACCCCACA CTCTGCCTGG CATCTTTCTA TGGTGATTCA 1140
CAGGTCAGGA GTGCACTCGT AAGCAAATGG AAGAAGGTAA GGAGAACAAG AGCTAATTAT 1200
CTGAGCTGCT TTTGAAATAA AGTGATATCA GAGAAGAAAG TATATTTGGC ACTAATCATA 1260
GACAGGAGAA AAATCCCAGC CACCCAAGAA 1290
|
