| Tag | Content |
|---|
EnhancerAtlas ID | HS182-05941 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr13:77890380-77891700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr13:77891461-77891480 | TAGCGCCCTCTGTTGGAAA | - | 6.56 | | EN2 | MA0642.1 | chr13:77891206-77891216 | CCCAATTAGC | + | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09931 | chr13:77890211-77891259 | CD14 | | SE_11254 | chr13:77869353-77891617 | CD20 | | SE_54458 | chr13:77890322-77891173 | Spleen | | SE_59820 | chr13:77871687-77914900 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I077316 | chr13 | 77890536 | 77890935 | | GH13I077317 | chr13 | 77891401 | 77891550 |
|
Enhancer Sequence | CAACTGTATT GTTATATATT CATATCAAAC AACTGAAAAA TAGGAAAAAC TAAACTAGTT 60
ACAGTAGCAC TAAAAACCAT AAAATGCCCC GATCAACCAG TTCATTCAGG CTGCCCCCAA 120
GAATGATCCA TCACCTAGGG CCATCACCTA TTGCCAAAGG CAATGCCCAT ATTGGAACTA 180
GGGAAGAGTC TGTAGCCAAC CAATGTTCCC AGCAGTCGTG GGGGAATTTT GAGCACATCA 240
GTGCTGGGCA GGGGCTCTGG GTTCCACAAT ACAGGATTCA CTATATTTCG CCTATTATAC 300
AATTAGGATT CACTTGCTTC AAATAAGGCA TGGAAAAAGT TCCTCCAGAA TTCTGGTGAG 360
TGTCATTTCC TGGAGAAACT TTCCAGAGGA AGGAAAGTGG GTCAAACCAC AGCCCCAGCC 420
ACTACAGACG GTAAAATTGA TATCAACAAC TCTTCTCTAC TAGCCATTCT AGATTCCTTT 480
AATCTATGGC TAGTATTTCT GTTGGTCCAG GTGGCTGACT TCATGGGGTG GTCACTGGGC 540
CTTTCTCGTG TCCATTTACC ACAAACACTG GACAAGGAAG TACCAAGAGA CACCTTATAG 600
ATCACCTGTG TGCCAAACCT CCATGCTCCA CTGTGGAACA CAGCCCTACC TCCTCCACAT 660
GAACAAGGAC ATTAACCCTG TCCAAATGGT GACTTCTTTT TTTGTTGTTT TTTTTTTGTT 720
TTGAGATGGA GTCTTGCTCT ATTGCCCAGG CTGGAGTGCA GTGGCGCAAT CTCGGCTCAC 780
TGCAACCTCC ACATCCCAGG TTCAAGCAGT TCTCCTGACT CAGCCTCCCA ATTAGCTGGG 840
ATTACAAGCA CGCGCCAACA TGCCCGGCTA ATTGTTTTGT ATTTGTAGTA CAAACAGGGT 900
CTCACCATGT TGGCTGAGCT GGTTTCGAAC TCCTGACTTC ACGTGATCCA CTCATCTCGG 960
CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCATCGTGC CCAGCCTGGT GACTTCTTTA 1020
TTTAGAAAAG GAGCCCCAAA TCCTAGTGGC AGCTGTACTT TAAAGTATAA CAGGATTCTC 1080
ATAGCGCCCT CTGTTGGAAA TGTTTCTCTT CTGAGAACCA GGATCTTTTA ACCCCTTGCC 1140
ATCAGAGCTA TGGAGATGGG AAGCAGAAAC TGCCCAGGTG ATTCACAGAG TGATGCTATG 1200
CGGAGCCACT CCTAATTTCA TGTGATCTTC CTACTGGGAA CACTGGAGAA TGGGCGCCTC 1260
ACCCTTGCAG GGCATCATGC CCAAGCTGCA GGATCTCATC ATCAGCTGTG CCATCAAAGG 1320
|
