Tag | Content |
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EnhancerAtlas ID | HS176-41102 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr9:4237510-4239000 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I004237 | chr9 | 4237321 | 4239085 |
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Enhancer Sequence | GGCATGGCTG AAAATCTACA AATGGCATCA TTATCATTCA AAATGATAGT ACTTTTTTAA 60 ACCAGCTGTT TCAGTGTAGC ACTTTCATTA CCAAATTCTG TTACCATTTT TACCCCAATT 120 CCATAAATGT ACATTTAGAA GTACAGTTTG TCAAACTGTT GATTCTCACC ACTTGATTCA 180 CCCTCTCATT AATCAGGCAT GCCTTTTGTT TTGCAGTATT TTCCCCACTG TTTCATTTGA 240 GATTAACTTT AAATTGAGAA AATAACTACT GACAGGTTCT TTTCTCTCTT CCTGTTTTGG 300 GACACACTGT AAGCACATTT TGTCTTTCCC AGTTCTCTCC AGCTTCAGCA TTTTATCAGT 360 TTGATGTGGC TTTAAACAAC TTTCCCTTCC CTAGTTAATT CACTAGCCCA GCAGCTGCAA 420 GGGACAAGAT GAATCCTTTC CATGTTCCCC TTATTCTCCC TTTGAGCAGG GACTGTCCAG 480 AACTTCCTCA GAATTTCTAC CTAGGAATGT TCTAGACCAG AAATTTTCCT CAGGAATTTC 540 CTGTTGCCAC CCTGTCCTGC TTCTATACCA GTGAGCACAA AGTCAGGAGT AAGCCTTTAG 600 GACCACTCCG TAAAAAAGCA ACTGGGACTT CTCGTTCCTA CTTTACATAA AGTTTATTCC 660 CTGCCCCCTC CCGCTGCGCA AAGAGCTTCC TGAGAGACCG AAACAATGTG GCTAAAAGGA 720 AGGCCAAAAG GAGGGAGGTG ATCTCTTAAT AGAACTCAGT ATTTAATCCT CCCCCACCCC 780 TAAGCTCTGC CCAGAATAGA TGACACAGAA GGAGAGGGAA TTGTTGTTTT GGTGGAGAGG 840 AAGAATATGA CCGTGAATAT ACTCCATTCT ATTTGAGAAT GAGAGAGTCT ACCCACATGA 900 GAGAAGATGT AAATCATCCC CCAACATTCT AACTTCCTTC CTGAAATACA CCTAGACCTA 960 GCAGTTTACA ATAATTTTTA AAAAGTGCCA AATATGCCCC CAACTTACAG TGCTAAAACC 1020 ACCGTGGCTA CCTGAACTCA GAAGGCCCGT GTGAAGCAAC CAAAGAAAGC TTAACCCTTT 1080 CTGGGAAGTA GAATAAGTTT TGCCAGTGTT CTCTCAGTTC TTCATAACCA AAAACAAAAC 1140 AAAACAAAAT TTACTGAGCA CATGTTCTGT CTGTGTGTCA TTCCTCATGA GTCAGACACC 1200 TTCTTATCCA CTATACTGTG TGCCCACTTG ACATCTTTCT TCCAGAGTTG GCTTTAATTA 1260 AATCCTTCAG CACTAATGTC CCAAAGCATT CCGTGAGTCA AGCTTTCCCT GGGGTTAAGA 1320 CTTTTGAAAT GACCAGCAGA GAGATGGACT CTAACTACTA AGACTACTAT AGCCACAGCA 1380 GCTACTGCAG TGACTTTTTC ACCACGAGGC AGCCAATTCA AAACAAACGT TGTTTTTTGT 1440 CCCTGCAGTA GTTTGCTGAG AATGATGGTT TCCAGCTTCA TCCATGTCCC 1490
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