| Tag | Content |
|---|
EnhancerAtlas ID | HS048-14996 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:87918480-87919700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:87918497-87918508 | AGTGACTCATG | + | 6.14 | | ONECUT2 | MA0756.1 | chr16:87918902-87918916 | TAAAAATCAATAAG | + | 6.03 | | ONECUT3 | MA0757.1 | chr16:87918902-87918916 | TAAAAATCAATAAG | + | 6.51 | | RUNX1 | MA0002.2 | chr16:87918917-87918928 | AAACCACAGAC | - | 6.62 |
|
| | 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 |
| GH16I087884 | chr16 | 87918485 | 87919684 |
|
Enhancer Sequence | TGATCCAGAC CCGACTCAGT GACTCATGCC AGTAATCTCA GCAGTTTGGG AGGACGAGGC 60
AGGCGGATCA CCTGAGGTCG GGAGATCGAG ACCAGCCTGA CCAACATGGA GAAACCCCGT 120
CTCTACTAAA AATACAAAAT TAGCCAGGCA CGGTGGTGTA TGCCTGTAAT CCCAGCTACT 180
TGTGAGGCTG AGGCAGGAGA ATCACCTGAA CCCGGGAGGT GAAGGTTGCA GTGAGCCAAG 240
ATTGCGCCAC TGCACTCCAG CCTGGGTGAC AAAGCAAGAC TCCATCTCAA AAACAAAACA 300
AAACAAAACA AAACAAAACA ACAACAACAA CAAAAAAAAG AGGGTGAAAG GCAGCCCCAG 360
AGTGGGAGAA GAGATTTGTA AAATGGACAA AGGCCTTATA ATTGGAATAT ATAAAGAACT 420
CCTAAAAATC AATAAGAAAA CCACAGACAG CCCAAGAGAA AAATGGGCAA ATGGCTCAAG 480
CAGGTATCTG GTGAAAGAGG ATATGCAGAC GGCCAATGAA TCTGCACAAA GTGCTCCACG 540
TCATGAATCA TTAGGGAAGT GCAAATTAAA TCCACAGGAG ACACCTGGGC ACACCCTCCA 600
GAAAGCACAC AATGACCTGC TGGCAAGGAC AGGAATGACC ACTTTGGAAA ACTCTTTGGC 660
AGCACAGCCG AACTGAGCCT CTCCACTTGA AAATGCCCTT TGCTCAGAAC CCAGCAGCAG 720
CTCCAAAGTC TCCACCCAGC CTGTGGGGCC CCAGTACCCA CCCTTGCCTC CCATGCCTCT 780
CTCCTCACCC CTGCACTTGG CTGCCCTCAC CCTCGGGCTG CACCTTGAAC ACCAGAAGGG 840
CGCTCCTGCC TCCAGCCTCT GCCTGGAATT CTCTGCCCTT GGGTAGCCAC GTGGTTCACT 900
CCTCCTTTGG TCTCTGCCCA AATGGCCCCT GTAGAAGAGA CCTCCCCACC CAGCCATGTC 960
CTCTTCCTGT GACTTACCAC TCCAGACTTT CTGTGTGGAT GCATCATGGT CTACCTCCTT 1020
CCATCAGAAT GTGAGCTCCG AGGCAAAGGC TCTTCAGACC TTAAACAGTC TAGGCTCCGT 1080
CCCCAGAGTC TAGAATAGAG CCTGCCACGT AATTGGCACT CAATAAATGT TACATGAATT 1140
AATGGAAACC ATCCTGGCAC GAGTGGTAGC TCTCTTTCCT CCAAAAGAAT GAGCTTGCCG 1200
AGAGAGACAA CATCATGAAA 1220
|
