Tag | Content |
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EnhancerAtlas ID | HS095-30442 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr9:4237410-4239040 |
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 | ACAGGTATTT TAACATAAAT ATGCAAAAAA TAAAAAAGTA GTAGTTTTAC ATGAAAGATA 60 GATGAAATCG CTACTTCAGG CTCAGTCTAC TGAGCCCTAG GGCATGGCTG AAAATCTACA 120 AATGGCATCA TTATCATTCA AAATGATAGT ACTTTTTTAA ACCAGCTGTT TCAGTGTAGC 180 ACTTTCATTA CCAAATTCTG TTACCATTTT TACCCCAATT CCATAAATGT ACATTTAGAA 240 GTACAGTTTG TCAAACTGTT GATTCTCACC ACTTGATTCA CCCTCTCATT AATCAGGCAT 300 GCCTTTTGTT TTGCAGTATT TTCCCCACTG TTTCATTTGA GATTAACTTT AAATTGAGAA 360 AATAACTACT GACAGGTTCT TTTCTCTCTT CCTGTTTTGG GACACACTGT AAGCACATTT 420 TGTCTTTCCC AGTTCTCTCC AGCTTCAGCA TTTTATCAGT TTGATGTGGC TTTAAACAAC 480 TTTCCCTTCC CTAGTTAATT CACTAGCCCA GCAGCTGCAA GGGACAAGAT GAATCCTTTC 540 CATGTTCCCC TTATTCTCCC TTTGAGCAGG GACTGTCCAG AACTTCCTCA GAATTTCTAC 600 CTAGGAATGT TCTAGACCAG AAATTTTCCT CAGGAATTTC CTGTTGCCAC CCTGTCCTGC 660 TTCTATACCA GTGAGCACAA AGTCAGGAGT AAGCCTTTAG GACCACTCCG TAAAAAAGCA 720 ACTGGGACTT CTCGTTCCTA CTTTACATAA AGTTTATTCC CTGCCCCCTC CCGCTGCGCA 780 AAGAGCTTCC TGAGAGACCG AAACAATGTG GCTAAAAGGA AGGCCAAAAG GAGGGAGGTG 840 ATCTCTTAAT AGAACTCAGT ATTTAATCCT CCCCCACCCC TAAGCTCTGC CCAGAATAGA 900 TGACACAGAA GGAGAGGGAA TTGTTGTTTT GGTGGAGAGG AAGAATATGA CCGTGAATAT 960 ACTCCATTCT ATTTGAGAAT GAGAGAGTCT ACCCACATGA GAGAAGATGT AAATCATCCC 1020 CCAACATTCT AACTTCCTTC CTGAAATACA CCTAGACCTA GCAGTTTACA ATAATTTTTA 1080 AAAAGTGCCA AATATGCCCC CAACTTACAG TGCTAAAACC ACCGTGGCTA CCTGAACTCA 1140 GAAGGCCCGT GTGAAGCAAC CAAAGAAAGC TTAACCCTTT CTGGGAAGTA GAATAAGTTT 1200 TGCCAGTGTT CTCTCAGTTC TTCATAACCA AAAACAAAAC AAAACAAAAT TTACTGAGCA 1260 CATGTTCTGT CTGTGTGTCA TTCCTCATGA GTCAGACACC TTCTTATCCA CTATACTGTG 1320 TGCCCACTTG ACATCTTTCT TCCAGAGTTG GCTTTAATTA AATCCTTCAG CACTAATGTC 1380 CCAAAGCATT CCGTGAGTCA AGCTTTCCCT GGGGTTAAGA CTTTTGAAAT GACCAGCAGA 1440 GAGATGGACT CTAACTACTA AGACTACTAT AGCCACAGCA GCTACTGCAG TGACTTTTTC 1500 ACCACGAGGC AGCCAATTCA AAACAAACGT TGTTTTTTGT CCCTGCAGTA GTTTGCTGAG 1560 AATGATGGTT TCCAGCTTCA TCCATGTCCC TACAAAGGAC ATGAACTCAT CATTTTTTAT 1620 GGCTGCATAG 1630
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