Tag | Content |
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EnhancerAtlas ID | HS045-04503 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:180182350-180183520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE41 | MA0636.1 | chr1:180182706-180182716 | GTCACGTGAC | + | 6.02 | BHLHE41 | MA0636.1 | chr1:180182706-180182716 | GTCACGTGAC | - | 6.02 | MITF | MA0620.2 | chr1:180182702-180182720 | CAGGGTCACGTGACTAAT | + | 6.77 | MITF | MA0620.2 | chr1:180182702-180182720 | CAGGGTCACGTGACTAAT | - | 6.77 | USF1 | MA0093.2 | chr1:180182705-180182716 | GGTCACGTGAC | - | 6.14 | USF2 | MA0526.2 | chr1:180182702-180182718 | CAGGGTCACGTGACTA | + | 6.66 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 180182841 | 180183144 | chr1 | 180182549 | 180183199 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I180213 | chr1 | 180182536 | 180182962 |
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Enhancer Sequence | ATTCCTATCT GTTAGGAACT TAGAAGAAAA GCTTGAAACA TTATCCATCA AATTCCTACT 60 GGTAGTTACT TCTGCAGAAT AGAATTTTAC AGTAGTGGGG GGATATTCAT TTGCTACTAT 120 AGACGCTTAG ATGTTTGAAT TATTTGCAAA GCATGTGTAT TACTTCTGCA AGAAAAATAA 180 AATAGGGAAA ATTTCTACTT CAGCAAAACG ACTATCTCCT ACTTATCAGA GCATTTCCAA 240 GTCACTCACA CATATTTGAA CATTTGAATG TTAAGTCCAA GAACACTGGC AGAGGCAATC 300 ATGCTCCCGC CAGTCCATCG GCTCCCCAGA TTTTCAGGCT CCAGCCGGGA GTCAGGGTCA 360 CGTGACTAAT TCTAGCCAAT GAGATGGAAG CGAGCGCCAC CTCCCGGAAA GGAAATGATG 420 CCCGTAACTT AGAGCGGGCT AAGGTGCTCA ACTCTCCAGT TTCCCTTCGT CTGTCTTGGC 480 CACAAAGGAA ACCACACATT CTAGATATAA AATGTTAGAG CCACCTGCCA AACACTGTAC 540 TTTTGTTATG CCACTGAGAT TTGAGGGTTA ATCTGATGCG GCATTGTATT CTGGCCTATT 600 TCAATTCTCT ACTGCTATCT GACAAACCAC CCCAAAATGT CTTAGCTTCA AACAACACTC 660 ATTTTCTTTG CTCATGACTC TGCAGTCTGG GCTAGTTTCA GCTGGGCAGC TCTTCTGCAG 720 GTCTTGCCAG GGTCATTAAT GTGGCTGCAT TCAGCTGGCG GGCAGGCTGA AGGCTGGGCT 780 TAGCTGAACT CACAAGACAG CTGGGCCTTT CTCTCCCCAC CCCCGTCTCT CTCCCCACTC 840 CCCGCCATAT AGTGTCTCCA CAAGGCCCAA GGTCTCTCTG GTAAAGTAGT TGGACTTCTT 900 GCACAGATGG GGGCTCAAAG CTCCCTAAAG TGCCATGCCA TCTTAAAACT TAGTCCCAGA 960 ATGGGCACAG TGTTACTTCT GGTACCTTCT GTCGGTTAAA GCAAATCACA GGTCCAGTCC 1020 AGACTCAAGA AAAAAGGACT CCACAAGAAC ATTCAAATAT CAGAGATGTG GTTCATTGGG 1080 GCCACCTGTG CAACACAGTG CCATGGCCTC TTCTGAGCAG TATAAACACC AAGGGCCTAC 1140 TCCATATGGG AGAATGCTGT GTTGCACACA 1170
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