| Tag | Content |
|---|
EnhancerAtlas ID | HS098-56648 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr9:4237550-4238920 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr9:4238763-4238774 | TTAATTAAATC | - | 6.02 | | STAT3 | MA0144.2 | chr9:4238587-4238598 | TTTCTGGGAAG | + | 6.02 |
| | | 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 |
| GH09I004237 | chr9 | 4237321 | 4239085 |
| Enhancer Sequence | AAATGATAGT ACTTTTTTAA ACCAGCTGTT TCAGTGTAGC ACTTTCATTA CCAAATTCTG 60
TTACCATTTT TACCCCAATT CCATAAATGT ACATTTAGAA GTACAGTTTG TCAAACTGTT 120
GATTCTCACC ACTTGATTCA CCCTCTCATT AATCAGGCAT GCCTTTTGTT TTGCAGTATT 180
TTCCCCACTG TTTCATTTGA GATTAACTTT AAATTGAGAA AATAACTACT GACAGGTTCT 240
TTTCTCTCTT CCTGTTTTGG GACACACTGT AAGCACATTT TGTCTTTCCC AGTTCTCTCC 300
AGCTTCAGCA TTTTATCAGT TTGATGTGGC TTTAAACAAC TTTCCCTTCC CTAGTTAATT 360
CACTAGCCCA GCAGCTGCAA GGGACAAGAT GAATCCTTTC CATGTTCCCC TTATTCTCCC 420
TTTGAGCAGG GACTGTCCAG AACTTCCTCA GAATTTCTAC CTAGGAATGT TCTAGACCAG 480
AAATTTTCCT CAGGAATTTC CTGTTGCCAC CCTGTCCTGC TTCTATACCA GTGAGCACAA 540
AGTCAGGAGT AAGCCTTTAG GACCACTCCG TAAAAAAGCA ACTGGGACTT CTCGTTCCTA 600
CTTTACATAA AGTTTATTCC CTGCCCCCTC CCGCTGCGCA AAGAGCTTCC TGAGAGACCG 660
AAACAATGTG GCTAAAAGGA AGGCCAAAAG GAGGGAGGTG ATCTCTTAAT AGAACTCAGT 720
ATTTAATCCT CCCCCACCCC TAAGCTCTGC CCAGAATAGA TGACACAGAA GGAGAGGGAA 780
TTGTTGTTTT GGTGGAGAGG AAGAATATGA CCGTGAATAT ACTCCATTCT ATTTGAGAAT 840
GAGAGAGTCT ACCCACATGA GAGAAGATGT AAATCATCCC CCAACATTCT AACTTCCTTC 900
CTGAAATACA CCTAGACCTA GCAGTTTACA ATAATTTTTA AAAAGTGCCA AATATGCCCC 960
CAACTTACAG TGCTAAAACC ACCGTGGCTA CCTGAACTCA GAAGGCCCGT GTGAAGCAAC 1020
CAAAGAAAGC TTAACCCTTT CTGGGAAGTA GAATAAGTTT TGCCAGTGTT CTCTCAGTTC 1080
TTCATAACCA AAAACAAAAC AAAACAAAAT TTACTGAGCA CATGTTCTGT CTGTGTGTCA 1140
TTCCTCATGA GTCAGACACC TTCTTATCCA CTATACTGTG TGCCCACTTG ACATCTTTCT 1200
TCCAGAGTTG GCTTTAATTA AATCCTTCAG CACTAATGTC CCAAAGCATT CCGTGAGTCA 1260
AGCTTTCCCT GGGGTTAAGA CTTTTGAAAT GACCAGCAGA GAGATGGACT CTAACTACTA 1320
AGACTACTAT AGCCACAGCA GCTACTGCAG TGACTTTTTC ACCACGAGGC 1370
|
| |
|
|
|
