| Tag | Content |
|---|
EnhancerAtlas ID | HS118-12448 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr3:13264650-13266880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr3:13265321-13265339 | GAGAGGAGGGAAGAAAGG | + | 6.03 | | NFYA | MA0060.3 | chr3:13265731-13265742 | GACCAATCAGA | + | 6.14 | | NR2F1 | MA0017.2 | chr3:13266633-13266646 | CCCATGACCTTTG | - | 6.48 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 13266466 | 13266631 | | chr3 | 13265200 | 13265970 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I013223 | chr3 | 13265002 | 13266090 |
|
Enhancer Sequence | TGACTCTCCA CACTCCCTCA GTAATACCCC AGAATGTCAG GTCTTCATGG AAAAGTCAAC 60
GCTTCCTGCA TAATTGGCTT CTTCCCAGTT AGAGGCATGA GCTCTGGGAG GAAATAATGG 120
AAACATACAA ACTCAGGTTT AGACTGGATC CAAAAGGCCC AAACCCTCCC ACAAGGATGG 180
AGATCTTCCA GATTGCAGGG AGGTCCCCGG GTCTCTGCTT CCCCACCTCC AGAGATAGGA 240
GCGCGCCACC TCCTGGCACA GCCTCCACCC CTGGGGAGTG GAAAAGCTTC TCCGCCCACC 300
CAGCAGAGTC CTCCCTGCTG CAGAGGGAGT CCTTGAGGCA GAACTCCTTG GGGATGGCAG 360
CCCTTCTCAT CAGAGGGAAG CTGGGAATGG GGGACAGGTG GGTAGGTCCC ACCCTCCCAG 420
CAGAAGGGCA GGAAAAACTG GCCTCCCAGG TCCTCGCGCG CCCACCTTCC CCATGCACCC 480
ATCAGCCAGA TCTGAGAACG CAAGTTCCTG CCCACAAGAG ACACACTGGG GACATGCAGG 540
GACCGCGGCG TCTGCAGAGG AAGTCAAAGC AAAGGCATTA GCAGGAAGAG GAAAAGCTGA 600
TTCATTTTTG AGCTGCATTC CAGACTTTAC ACCTGGCCCA TCTCAGCATT TTCTAAATGG 660
ACAGACTCAG AGAGAGGAGG GAAGAAAGGG GACATCTTGT GCCCTAGAAA TTCACTGCCC 720
AGAGCTCCCT CCTAAGGCGC TGTTGGTTTG GAGTCACCGG ACATTAATGA GCTTTGGAAG 780
GGAATGTTGG TCAGCACAAA GCAGTGCCTC GGAGCCAGGC TCTGAGCCAG GGGGTTGGGG 840
CCGAGTCCTC CCTCAGCCCC AGAGCTGCTG GGTGACCTTG AGCAAGTTGC TCAATCTCCA 900
GTTCCTTATC TGAGAAATGG AAGCAATGAG GAGGCCAACC TCGGGAGGCT GCTGGGAGGC 960
TTCAGTGGCA AAGGCAGGAA GACTACACAA TCCAGGGCCG GTGCAGAGCG AGAGCCTACC 1020
ACAGGGGCCG TTAGAGCCGA CATCGACCTC ACTACCAGGA ATGAGTCCCC TCTGTGGTCC 1080
AGACCAATCA GAAGGAGGGA GAAGACAGAG GTCCTGCCCG AACCCAGGAG GTCAGCAGGA 1140
AGAAAGAAGC CCCCACACCC AATTATCAGG CCCCGAGAGG AAGGGTGGAA GGGCCTGGGA 1200
GGAGAATGAC TTCTGCCTTG GGGATCAATG TGGGCATCAC TGGTCTCCTA GTTCTGGGCC 1260
CTGGGCCCAG CCCAGGCAGG GACCGCCTGC TGTCCAGGGT GCAATGGGAG AAGGGGCGCT 1320
GGGCAGACTG TTGAGGGGCT TCAGCCTTGT GACATCCTCT CAGCCAATCC ACTTTTCCTT 1380
TAGCTTTCTG AGTGCTGAAG CAGCCCCCTG AGAGCATCTG ATCTCCGCAG TGCTCACCAG 1440
GGCATGTCTT GGGGTTCGAC TTGACGTTCA GTGCCACAGG CCTGACCTAG GCCACCGCCC 1500
ACCAAGATGG ACCCAGGACG GGAGCATAGC CTGCCAGGAG GGTAGCTTCG ACTGTTCCTC 1560
TTCTGTAGTT GCCCACATGG CCACATGGGA GCCATCTCCA TTGTCAATCC CCCCGCCAAC 1620
TCCCGTGACC ACACAGGTGC AAGGAGACCA GAGGCACATC AGGCAGGTAT GGGAGCTGCC 1680
CTGGCTTAAA AGCCTCATGC CCCCCAGAAG CCAGCACCTC TACTAACAAT TCCATCAGCA 1740
AAGCATACCG GATGCCCCAC GGGGACGTGT CCAGCACAGA GTCACTATGC TCTGTGAAGC 1800
CCAAGCCTGG TGGCCCAGCA GGTACTCATA GCTCCCCTGC CCAGATACCA TTGTGCCATT 1860
AGCAATACTG CCCAGCAGTA GTGAGACATT CTGCCTTTAC CTGGTTCCCA GGGAAACAGA 1920
GCTAGAAAGT TAACCCGAGA TCAAATTCTC ATGCAGGGCA AGGGTTTTGC TACCATAGTC 1980
CGCCCCATGA CCTTTGGTCA ACACCTTCAC ATGGACACCA ATGCATTTTA CAACCACCAG 2040
GAGTTGTATA ACCCAATGGG GCATGAACGT CCCTTTTGTC CCCTAACCAA GTGGACTTCC 2100
CCTGTGGTCA GTTAGTTTTA TAGCCCCATG GTGCCTTTTG ATCCTGGGAT GAAAGGCAAT 2160
GGTACTTCGG ATAACACTAA ATGTGTGTTT AATGCACCAA AGATGGAACA GTGTTTTACC 2220
AGAAGCCACT 2230
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