| Tag | Content |
|---|
EnhancerAtlas ID | HS101-25876 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:213823400-213824580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr2:213824403-213824414 | CCACACCCTGC | + | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_39644 | chr2:213819382-213827354 | Jurkat | | SE_50011 | chr2:213819563-213829313 | RPMI-8402 | | SE_66647 | chr2:213819382-213827354 | Jurkat |
|
| | 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 |
| GH02I212954 | chr2 | 213819473 | 213826682 |
|
Enhancer Sequence | CACCTTTACT TTTTGTGCAG ACAACACAAT ATGGGAAGAA AAGTCATACT ACATAGCAGT 60
TATTAAAAAC AGTTAAATGT AACACCAGGC GTTAAAACCT AGTACCTTCT TGTCATGATA 120
AAGATTGTAA CAAGAACAGG AAATGGCACA GCACAAATCC GTTTTCATGA TAATGATCTC 180
GTGAATGTAA AGAGCATAGG AAATGGAACA AATGTAACCC TATTCCATTA CCACCTTCAA 240
ACGGTAACCT CCTTGTCCTA GTCACATGCC CTACTTATGG TCCTGATTAA AGCACAAAGG 300
AAATCATAAG ACTGTGACTC TGAGGGAACG AAGCAGCTCC CACTTATTTG TGTGCGTGTG 360
TGAGCACACA TCTTTCCTTC TTTGAACTAA GTTGCACCAG GCAATTCCTT ACAGCTGATT 420
CCCCAACTTT GTCCTGAATA AAGCCGGTCA GACATGGGAG GGACAAAGAA AGCTAAAAAC 480
CAATGAGTCA TCTGGGAATA GATGTTCTCT TTACTACCCT TTATCAGAAT GAGGAAATGA 540
TGCCTTCCCC CCAAATAGAG GCAGTAAACA GTGAAGATGA CTGAATGCTT TTCTTCTGTC 600
TAGCCTTCAT AGCACCTCAG CTTACCAAGG AAAATGGAGC TTCTATCTCA TAGTGAGTGT 660
GTTCTCTCTT CCCTACCTAA AGAGGCTGCA ACATGATTAG GGCTCGTCTA GAAGTACAAA 720
GGAAGATCTC AGGGACACAA GGAAGCCAGA AATAGTTGAG GTCAATCAGG CCAGGTTAGG 780
GTTGGTGCTG CCATACTATA TTCCTCTTTG ACCTGGGCAT GTTTTCCAGG AGGATCTATT 840
TCCCTTGGAA AGCTCTTTAA GTAACACTAT GTGAAATTTA TAATAAATCC TCTCACCCCA 900
AGATGACTGC TTCAGATATG AGGGGGAGTA GTGAGGAATG ATGGCTGAGT TTGCCAAATA 960
AATACGAGGG AAGATGAAAG CCAGATTGCC TGGAGTACTG TGCCCACACC CTGCCTCAAC 1020
CAAATGTCAC TCACTCTGCC CAGCTGGCTA GTAACTCCTT ACATGGCATC CAAGTATCTG 1080
TACTATACAT TTTCTTCTAC TGGGGCTTTG TCCAGGCAAG CAAGTCTGAA TGCACTTTAC 1140
ATTTCAGGCA TCTTGGATAT CTGTTCCTTC CAGATGATAT 1180
|
