Tag | Content |
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EnhancerAtlas ID | HS182-12395 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:69084310-69085930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr2:69085917-69085928 | TTAATTAAAAC | - | 6.14 | REL | MA0101.1 | chr2:69085323-69085333 | GGGGATTTCC | + | 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 |
chr2 | 69084387 | 69084602 | chr2 | 69085194 | 69085477 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I068857 | chr2 | 69084301 | 69085601 |
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Enhancer Sequence | GGTAGGGTTT TCAGGACTCG GTGTTGGAAA GACTCCCAGG AAAGGTAGTG AAAATGTCAG 60 TCAGTTCAGT TGAGAATCTT CTGAAGTTCT GGGGAAACAT GCCTCTTCCC CAGTGGGGGT 120 CGAGGAGGAA AGAAAAACCT CTCAGGTCCA TGTGATGTCT CCTCACTAAG GGTTGGGAGT 180 TTCCAGTTAG TTGACAGACA GATTTCATAA GAGAGGGAGG GGAAAATCCT GAAAAGACAT 240 AGCTGGCCAG GACCCTGGCA GAATGTTTGG GGCATGAGAT TAGCCAGCAG TGTCAGCCTG 300 ATTCCTCCTT GAGCTGTGGG CTGAGCATCT TGGTCTCACA CCCAACACCT TCTAGGCTCC 360 CAGCCTTGAG AGAAATGTCT GGGCAATTCT GATGAGGAGC CGAGAGGACT CAGAGACCAA 420 ATGAGTGCCC CAGGGTCTCT ATAGGGTTAT CCAACCTGTG CATATGACTC TGCTCTGTCC 480 TTGTCATCAC TCCGTGTCTA TCTCTGCAGA ATTCTCAGTG AGCTCTTAAC CTATGGGACC 540 CATACATTGA GAAAGGGCAG GAAGAGGAAG CACCTGTATT GCAGGGAGAA AACTCTTAAA 600 GATGTAGTAG TGAAGAACAG CTCCAAAGAG GGAAGGAAAG CAAGAGACAG GAAAAAGCCC 660 CAGGGGAGGG ATGGAAGTAT GGTAGGCAGC CTGGATCCTG AGGTATGAGG CCCACTCAGT 720 GTCGCCTGGC TAAAGCTTGG GGGTTTCCAG TTTGTTGACA GATTTTGTAG GAAAATGGAT 780 GTGAAAGTTC ACTACTTTTG TGGTTTTAAG TAGAAGGCAG CATGGCAGAG CAGGGAAGGG 840 CTTGATTGCT GGAAGTGAGC TGCTTGGGTT CGCAATCCTA CTTCTGCTTC TGCCTGGTTG 900 AATGACCTCT AAGAGTATGC CTTCTTCACT GTGACTCAAT TTCTTCACGT ATAAACTGGG 960 GATGATGATT TTGGGGTGTT ACTACTGTTT TTAGCATTGG CAGACATGGT CAAGGGGATT 1020 TCCACTTCAA ATCTCAAAGC TATTCTTCAA TGATGAACCT TACTAGAATA ATTTGTTTAG 1080 TGTAAACAAA TTAATGCTTT GTGATTAGTC ATCTTCTGAA TAGCCCTTCT AGGCATGGAA 1140 AGGCAAACGA CTTCATCTTT CTCTGGATCT TTCCACTCAT GTAACCTTCT GAGCAATACC 1200 TGACTTAAGC TGCCAGATTT AGCAGATAAA AACATCCAAC CAAATTTGAA TTTCAGGTAG 1260 TCAACCAACA TTATTTAGTA TAAGTATGTT CTGTACAACA TTTGAGACAG ACTTATACTA 1320 AACAAACTAC TCATGGTTTG ATCTTAGATT CATATTTAAT TGGACATCCT GTATTTCATC 1380 TGGCAACCTG ATATCTGACC CCAAACTGCA CAAAGCAGGT GAGCCTGGAC CTGGGGAGCT 1440 AGAATGCAGG TGTAATTCCC CGGTGTACAC CTCGCTCAGG CATAGTCTGC AACTGTGCTT 1500 TTGCAGGATC TCTTTTAAAA GCAAGAACAA CAACAACAAC AAAGAATAAA ACATGCGATA 1560 TTTGCAGCAA AAGACGTAAC AGGAGCTGGT CTCATGTAAA TATTACGTTA ATTAAAACAG 1620
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