| Tag | Content |
|---|
EnhancerAtlas ID | HS073-06466 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr17:56735680-56737120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr17:56736368-56736378 | TCTAATTAAA | + | 6.02 | | FOXA1 | MA0148.4 | chr17:56736663-56736679 | CATTATTTACTTAATA | - | 6.36 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_66919 | chr17:56735924-56737530 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGCCTCCCAA GTAGCTGGGA TTACAGGCAT GCACCACCTG TACCAGTGTG TACCACCTGT 60
GCACCGGCTT TTTTTTTTTT TTTTTTTTTT GAGACAGTCT CACTGTGTCA CCCGGGCTAG 120
AGTACAGTGG TGTGATCTCG GCTCACTGCA ACCTCTGCCT CCTGGGTTCA AGCGATTCTC 180
CTGCTTCAGC CTCCAAAGTA GCTGGGATTA CAGATGTGCG CCACCATGCC TGGCTAATTT 240
TTTTGTATTT TAGTAGAGAC AGGGTTTCAT CATGTTGGCC AGGCTGGTCT CAAACTCCTG 300
ACTTCAAGTG ATCCACCCAC CTCGGCCTCC CAAAGTGCTG GGTTTACAGG CTTTAGCCAC 360
CCTCAGCAAT TCATCCCACC AGAACAAAAG GCTAACATAG CAAACTGGTA AATTTATCTG 420
CACAGAAAAA CTGAACTACA AGGGATGAGG TACTTAACTT CCCACCTGAA GACCCAGGAA 480
TTTTTTTTTT TTACTTTTCT TCATTGAGAT AGGGTCTCTA TCGCTCAGAC AGGAGTGCAG 540
TGGCACAATA TTGGCTCATT AAGTCTCCAT CTGGGATCAA ATGATTTTCC CACCTCAGTC 600
TCCCGAGTAG CTAGCACAGG TGCGTACCAC ATCAGTCTGG CTTATTTTTC CACCCTTCCT 660
AGAAACGGTA TAAAATACTT AGCGAGCATC TAATTAAAAC AGACCGTAAC CTAAGAAGAC 720
GTAAGGTCAT AACCACAACT CCAAAACCAA ACGCGCGCCA CTACAACAAC TCTGAAAATA 780
AACACACGCA ACAACACACA AGCCGTCTTT TAAACTAGTT CAATCACAGG ACAGAAAAGC 840
GCAAAAGCAG TCCCCCACTA CCACAAGTTA TGCAGCCGAG TTTTCTCATT CGGGGAAATC 900
GCGGGAGCAA ACACATAGTA AAAACCCTCC CCCAAGAAAA ACACTTTATC AGGACCAACA 960
GCGTCTCTCC CCCGCCACAA AGACATTATT TACTTAATAT TGCTAATACC TTACCATCGT 1020
CCTCAACACA CAACATACTC ATGGCAAATT GTATTATGAG TTGTTTTTAG GCATCGCTTC 1080
GAAACTACCG CTTCTTCGTA TGACACATCT CAGACTACAC CTTCTTTGGT ATTCGCTAGA 1140
AAATTTCTCC CGCGAAGAAC GCACTAGAAC CGGCAATCAC TGCGCCCCTA TCTACATATG 1200
CCCGCCTCTT ATAGTAACGT CACCACCTGC TTCTGTACGA TCTGACTGAA CTCCCTTACG 1260
GATCGGTTCG CTCTAGCTGC CGCTCCCAAG GATTCAAAAG AAATCGCATT GTGTGATAAG 1320
AAATTTTTTT TCTTTTTTCT GCACAGGCTC ATATAATAGA AGTAACTTTT GTTATTTTTT 1380
CAGAGAATTC ATACAGCCAT TAATTATCCA AACCTATTTC TCAGTGCTTT TCAATGGCGT 1440
|
