| Tag | Content |
|---|
EnhancerAtlas ID | HS134-58624 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr8:23000690-23001960 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr8:23001518-23001529 | CTTCCCAGAAG | - | 6.14 | | Sox3 | MA0514.1 | chr8:23000985-23000995 | AAAACAAAGG | - | 6.02 | | TBX20 | MA0689.1 | chr8:23001406-23001417 | TTTCACACCTA | - | 6.14 | | TBX2 | MA0688.1 | chr8:23001406-23001417 | TTTCACACCTA | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATGTTGGCCA GGATGGTCTC CATCTCTTGA CCTTGTGATC CACCCTCCTC GGCCTCCCAA 60
AGTGCTGGGA TTACAGGCAT GAGCCACGGC GCCCGGCCGA CTGAGCACCT TTCTATAGTG 120
TGGCAGATGT GTGGCTCTGC ATTTACCACT TTCAAAAAAT GTGCAGCGCG GCCAGGTGCA 180
GTGGCTTATG CCTGTAATCC CACCACTTTG GGAGGCCAAG GTGAGAGGAT GACTTGAGGC 240
CAGGAGTTTG AGACCAGCCT GGGCAACATA GCAAGATCAG ATCTCTACAA ATTACAAAAC 300
AAAGGTGCAA TGCGATTCAG CAGCGTGGAG TAATTGTTGA TATTTTTTGT TTATTTCCTT 360
ACCTTTTTAT ACTTCCCTTC ATTAAAAAAA ATGGGGTATA GTTATAGGAA AGGAAGAAAA 420
TGGGTGGAAA GTGAACCTTG TCTAGGTAAG TATTTGACAA GTGATCAAAG AGGAGCCAAA 480
AGCAGAGAAA AATAGGAGAA TCAGTTCCTA AACAGGCGTG GAGGAAGGAG ACAGTGACTC 540
ACAACAATTC AGGGAATTCC TCACTTCACA CAGCATCACA AAAGAAATGG CACCTACGTT 600
CCACTGGTGT ATGCTACAAA CCAAATCATT CTTTAAAAGT CCACAAAAAA TTAGGTAGGA 660
TCATCTTATT TTATCCTGAA GGAAAGAACT TAAAAAAAAA CAAATGTGTG TCCAGATTTC 720
ACACCTACTC AATGTCATAT CAAAACTAGT GAATCGATGT GAATAACTGG ATGTGTGTGT 780
TTCTGTAATA CAAAAGCACT TCTACACACT GACTCAGAAA TCCTACTTCT TCCCAGAAGC 840
CTCCTTACAT ACTTGATCAG AAATCTGGAC AAAGATTTAC TGTGAAATAT GTTCAATGTA 900
GTAAGAATTT TGAAGAACAT TTAAAACTTC CGCTGTTTCA AGCAAGGGCT CCCTGACTTC 960
TGTTAGGAGC ACACGATGGA GACTGTGCAG CCTTATTCAG TCCTCAGTGA ACCCTGTGAC 1020
ACCCACTCTA TGCCTGTGGA GATCCAGGCT CTGGGGACAC AGCAAGGACA GGACAGGGAG 1080
TAAGAAGCAG ATGTCCTGCA GACTGGCACG GTCACCACCT CAGTGCAGCT GCTCCGTCCC 1140
CTGCAGTCCC CTGTCTCCCA AAGGCTCCAT GTCCCCTTGG GCCAGGAAAG AGGAGGCACT 1200
GCCATGTCCC ACTGTCTACA AAGTCCTGTG CAGGCTGCAC GCCAGGCAGG GCACAGTCCC 1260
TCCTCAACTC 1270
|
