| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11697 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr19:58282650-58284320 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr19:58284176-58284187 | TTAATTAAATC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 58283497 | 58283551 | | chr19 | 58282817 | 58283104 |
| Enhancer Sequence | AGAGAAAGAC TCCGTCTGAA AAAAAAAAAA AAAAGAGAGA GAGAGAGATG GGGTTTCGCC 60
ATGTTGCCCA GGCTAGTCTC GAACCCTTGG GCTCAAGCAG TCCTCTTGCT TCGGCTTCCC 120
AAAGTGCTGG GATGCCAAGC AGGAACTACC GCACCTCCTA GGACACTTAA GTGCCATTTC 180
TCCGGTCCTT CAATCTGGGG ATCTTGGAAA AACCTCAAAC CCCAAACCTA CATCAGTGAC 240
ATAGGTTATG GGGAGTTGTT GCTATGTCTG TCAACTAATG TAACACATGT GGAGGGTTCA 300
CCCAGGAACT GATACTGGGG TGTGCAAATA CTTACTTAGA AGTGAAACTA GAGGGGTGAG 360
GTGATGTTAC CAATTTCTTA ATAGGCGCTG TCTGGTTACT GAGTGGGCAA CAGACTGTGG 420
GGTTGAGGGA GGAGGAAGAT CAAACTGGAA GCTACTGCCC TAGTCGAGGT GAGGATTAAT 480
GGACTAGAGT TGTGGCTTAG GCAATGTGGC TAGATCTGGA TTTGTGTTTT TTAGAGGGGC 540
AAGTCAATTT TTTTTTTCCC AAGATGGAGT CTGGACCTGT TGCCCAGGCT GGAGTGCAAT 600
AGTGGAATCT TGGCTCACTG CAACCTCCGC CTCCTGAGTT CAAGCGATTC TCCTGCCTCA 660
GCCTCCGAAG TAGCTGGGAT TACAGGCGCG CGCCTCCACA CCCAGCTAAT TTTTGTATTT 720
TTAGTAGAGA CTAGGTTTCG CCATATTATC CAGGCTGCCT CGAACTCCTG ACCTCGTGAT 780
CCACCCGCCT TGGCCTCCCA AAGTGCTGGG ATTACAGGCT TGAGCCACCG TGCCCAGCCT 840
GGCAACTCAA TTTTTAAATG TGAACAGTGA GAGCTTGAGA GGATTCAGGA AACACCCCTG 900
GGTTTTTTAT CTTAGCAGCT GTAGCAATGG GAGCTGCATC AACTGAGATG AGCAAGTTGA 960
TAGCAGGTGT AATATTCACT GAGGCTATCA GGAGGTTTGT TTTGGCCATT CTGCGTGGAA 1020
AAAAATACAA ATTGCTTTTG CTCTGCTCTC CCCCACAACA ATCAACACAG AGTACTTCTG 1080
TGACTAGATA ATGTGTGGAT GGTTTTCCTC ATACACCAAG TAGTTCTGCA GTGGACATCA 1140
GATCCCACAG GGTGAAGTCT CAGTCCCACG GGACTGTCCG CCAACCCCTT TCGATGCCAA 1200
TCACAAGCCC CAGGATGTTT TTTTTTTTTT ACCTGTCCTT TGACTGACTT GATAAAAATC 1260
AGGTTCCCAT GACCCCTTCC TCGGCTTCCA TTAAATTGCT AGAGCCAGTC ACAGAACCTC 1320
AGGAGATGCT TTAATTTGCC AGTTTATTTT AAAGAGTATT TATTACAAAG GTTACAGATG 1380
AAGAGATGCA TAAGGGGAAG CGACCCAGAG CTTTTATGAT CTTCAGGCAC ACCACCATCC 1440
AGGAACTTCC ATGTGTTTGG CTATTTGGAA GCTCCCCAGA CCCTGTCTTT ATGGGGTTTT 1500
ATGGAGGCTT TATTACATAG GCATGATTAA TTAAATCATT GGTCAATGCT GATCAGCTTA 1560
ACTTTTGGCC CCCTCTCCCC TTTCTGGAGA TTGGGGTATG GGGCTGAAAT TTCCAGACCT 1620
CGAATCCTGA CATAGTCTCT TTTCCCTGAC CGGTCTCCAT TCTGAAGTTA 1670
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