| Tag | Content |
|---|
EnhancerAtlas ID | HS180-10298 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:129152450-129153900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr11:129153255-129153266 | AGCCACACCCA | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 129152943 | 129153736 | | chr11 | 129153000 | 129153200 | | chr11 | 129153200 | 129153293 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I129282 | chr11 | 129152563 | 129153810 |
|
Enhancer Sequence | CTATCACATT TTCATCATGA ACCTCTATCA TAGTAATTCA GAACTTTGTG TTATTCTCCT 60
ATGAAATTTT TTTTTTCAGT CTTTAAACCT TAACACCAAC TCCACCTATT GACATGTCCA 120
CTTTTGAATG GGGTCCTTGG CCTCCTCTGT GATTCTATCT GCTGCCTGCC CCAGGGCTCT 180
GACCGTGGGC CCCTCCTGTT CTCTTTCTAC ACTGCCACCC TAGGCAGCAT CCTCCAGCAA 240
GGCTTTAAGT AGCCTCTACT TTTAACCCTG GCCCCTCCCC AGCACTCCAC CCTCTTATAT 300
CCTGCTGCCT CCAGGCATCT CCATTTGAAT ATCTCCCACT TAATGTGTCT CAAACAGAAC 360
TTTTGATTTC CATATTGTAA ACAAAACCCA AAACTGATTC CTCCAAGTCT GCCTCATCAC 420
AGGACAAAAA ATATCTCTTC CTTTCAATCA CCACGTTCAT TTTAGCCTAC CTTCAAATGG 480
TACGGAAGCC AATCGCATCC TTCTCTCTTA ACCACGAACA CCCATGTCTG CCCTCCCCGT 540
GATCTTTCTC CTGGGTGACT GGGACAGACG AACCATCACC CTGCTTCCAC TTTTTCCCCT 600
CCACGGTCTA GCCTCTACAC AGCCACCAGA GAATTTATTG TAAAGCATTG GTAAGATAAT 660
GTCCTTGTTC TTGCCCAAAA CACTCCAGGG CCCTGTGCTT CTAATCACAC TGCAATAAAA 720
TCCAAAGTCC TTTCCCAGCC TTTCAAGTCC TTTCAGCCCT GACTCACCAG TTCAGTTTTT 780
TACCTTTTGC CATTCACTCT GCCTCAGCCA CACCCACCTC CCTCCTGAGG TTTCTCAGAC 840
CTGCCAGGAA GACTCCACCT TCCTGGCTTT TAAATTAACC TTCCTACTAC TATATAAAAT 900
AGTTCTGCCT TCTCTGTCCC CTTACTCTGC TTCTTTTTTT TCTCATAGCA CTTATCACTA 960
CATGATTATG TTGTGTAATC AATATTTATT ATTGGACTCT GTTCCTAAAA TGTAAGCACC 1020
ATGAGGGCCT GGACTTTGTT TATTCACAAA TGGGTATGTT TATGCCAAAT GAATACATAA 1080
ATGGTACTAT CAGGGTGCAA AGTCTTTATA CACACTTCTT ACCTGCTGTT GTGTATTGCC 1140
ATGGATCTAT CTTTATACTT AGTACAAGTG GAAACAATTG CAAAGTGTAA CATTATGTAA 1200
TTTAAATTTC CTGTACTTTC AGCTCTGACC TCTCCCCAGC CCTCCAGCCT CATATATTCC 1260
ACAATAAAAT TATATCATTT GCAGTGCACT GCAAGTCAAA TCAAGACAAA CTATACTGAA 1320
AATCTAAGAA AATATCAAGA TTCAGCAGAG AAAGGTACAT ATTACATGAG GAATTTAGTG 1380
CCCGTAGGAC AAAATCACAG TCTAACCTTG CAATTAGGTT TTAATATGTA GAAATTAAAG 1440
GCACAGAAAA 1450
|
