Tag | Content |
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EnhancerAtlas ID | HS088-01836 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:44228670-44229800 |
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 | chr1:44228836-44228847 | TTAATTAAATC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 44229452 | 44229714 | chr1 | 44229038 | 44229664 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I043763 | chr1 | 44228701 | 44229826 |
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Enhancer Sequence | TGGACCCAGC ATTTCCACTT CTAGGAATTC CCCTACTGGG ATTCTTGCAC ACTTGCAAAA 60 TGATATATGC ACAAGGTTAC CCATCGCAGC ACTTTGTTTA TTTGCAGCAT TGTTTTTAAT 120 AGCAAAAATT TGGAAGCAAT TAGAATGTTT ACCAGTAGAG AACAAGTTAA TTAAATCATG 180 GTTCCCCCAT CCGGTGAGTA CTCTGCACCT GAAGATGAGG AGGCTCTGTA TACACTAATA 240 TGAAAAGATT TCTGAAATAT ACTGTTAGGT GTAAAAAAGC AAGGATGGGG AGTTTTCTTT 300 GGGGCTTATA ATGTTTTAAA CTTTTATCAT TGTTGTAAAT GGATGTAGCT GGTTGTTATA 360 TTCCTTACAA TTACGAGATA CTGGGTTCTT GGGTTTGTTT TTCTATGAGT TCTAGTATTC 420 TGTTATTCTT TCTAACTTTC TTATTATGAG CAATAGTTGG CATGGAGGAG TGGCGGATCA 480 AATTTTTAGG TTATTAAATA GGCTCCATTT CAAGCCAATC AGCGTTGCCT TCTGCTGTTT 540 TGTGCCTGGC TGCCAAGTGC CTTTATATGG TGTTTCAGCT TTTTAATGGA GCTTTGATAT 600 GTAGCAGTCA CCCTGAGCCA CAAGAGGGCA GAAGAACCTT TTGATTGCCA CAGGACAGAT 660 TAGCGCTGGA ATGACTTCTG GCAAAATCCT GCATGGAGTA GTTCTTCAAC TCACTTACTA 720 GACCGTGGGC ATCCAAAGGC AGGCCAGTGT CTAAGCCATC AGAGGAGGCA ATGGAGGGGT 780 GAGAGGAGAG AGTGTGTGTT TTGGAATCCT CTATATCTGC CTTATGTTCC AGGCTCCCCT 840 GCAAATTACT TAGTGAACTA TACTCCTTAC AGTGTTAACC TCTCTCAGAG CTTGAATATG 900 CAAGACAGTA GAGGCATTAC AACATAGTGG AACATAAGAG TTGAGGCTTT GGAATCCACC 960 CCACCTAACG TTGAGTCCTG GCTATGTGAC TTTGGGTCAT TTCTTAACTG TCATTTATTC 1020 AATGAGATAG TGTGTGTAGA GCTCTTAGCA CTGTGTTGTG AACACTCAGA AAGTAACTGC 1080 TATAATTACA ATAGTACAAG GTATCAGCAC AGATGAATAA TATTAATAGA 1130
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