| Tag | Content |
|---|
EnhancerAtlas ID | HS182-17221 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr4:153877750-153879540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr4:153877991-153878002 | CCACACCCTCC | + | 6.32 | | Myod1 | MA0499.1 | chr4:153877875-153877888 | AGCAGCTGTTTCT | + | 6.28 | | RREB1 | MA0073.1 | chr4:153879254-153879274 | TGGGTGGGTGTGTTTGTGGG | - | 6.24 | | Tcf12 | MA0521.1 | chr4:153877874-153877885 | CAGCAGCTGTT | - | 6.32 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24471 | chr4:153877686-153879481 | Colon_Crypt_2 | | SE_25160 | chr4:153877676-153879894 | Colon_Crypt_3 | | SE_28188 | chr4:153874781-153880929 | Fetal_Intestine | | SE_28967 | chr4:153874632-153881633 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I152953 | chr4 | 153875050 | 153880659 |
|
Enhancer Sequence | CAGGCACTGC CTTGAATCCC CGAGACTCTG TCACCCCCAG TTAGCTAACC CGGGAGATGG 60
GGTCCTGCTG AAATGAAAGT ATTGGCCTGG GACCCTGAAG TGCCTTCCCA GCCACTGAAC 120
CAGGCAGCAG CTGTTTCTCC CCACAACCTC CTGCTGCGGG GTCATCCTCA GTCTGAATAT 180
CTGGCGTGCT TGGTCACACT TCGCCTCCTT GTTTACATTA CTGACTCTGA GCTTCAGCTC 240
ACCACACCCT CCAAACTCAA CTGGGAGTTT CCTTCAGCAG GAACACCCTG ACAGTCCCCA 300
GAGCCGGCAG GAGCCCCTTC CTAAACCCTC CCGGGTATCT GTGCTGTGGG AGGGGGTCTC 360
GGGGAAAGCC GAAGCCGCTC CCTGACTGCT GCCCACTGTA AGGACAAACT TTTTTGTGTC 420
CCCTGGCACC AGTCAGACCC AGGGCCAACC CTGGAGTCTT TGGGTCTCTG GATGGAGGTT 480
GGAGGATGCG GAAGAGGCCA AGGAGGAGAC AGGGCCAAAT AAGAGAGGTT TAGGAATGTG 540
GCAGAAATAT GCTAATAAAT TCGTAAGTGG ACACATTACC ACGTGGCTCT CAGCCTATGT 600
GTAACGCTCT GTGCTCATTT TTAGCACAAG TAAGGACTAA ACCTTTATTG AGTGCCCCCA 660
TGTACCAGGC ACTGACTGGA CAGGGCAGAA TGAAGTGACT GAGCCTAGTG CCTGGCACAT 720
AAAAAAATCA ATCATAGCTA TGATTCTTTT GTGTATTTTT CATTTAATCC TTGCAGCAAT 780
GTTTTAAGAC ACTCCTTGTT TTACAAATGA GAAACTGAGG CTCACACAGG TTAGTTATAC 840
CTTGTCTGGT GTCACATGAT TGCTGAGTGA TACAGCAGCG GGGTGGACTT GAGCCCTGAT 900
TCCGCTGAGC CCAGTGTGGT TCTGCTGCAC TCCACTGCCT GCCTTGGAGG AAGGAAGGGC 960
AAAGGTTGTC AAAACCCCGC CTCGCGCTGC TGGCCTGCCA GCCTTTTCAT CACCTCTGCT 1020
ATCACAAAGT ACTGGTGTGA ATAAGTGTCA CTTGAATAAT ACTGTAATCT TATCAGCATG 1080
CTGAAAGATA TAAACGGAAA CAGCCCTTTT CTCTCCTGCC TTCTCAGCTG ACAAGCCGAC 1140
CAAAGCCAAG GTTAATTCGT TGTTGAGAAT TTCTCTGCCC TCTACCACAA ATCTTTTATC 1200
TGGCATGTTT GTTCATCTTT CCTCTAATAG AGGTTCACAC TTGCAGAGGA AGAAGGTGGG 1260
CCCAGAAATG AAACTCTGGG AGTGTGTTCT TGTCCAGCAC GGAGTTCCCA AGCCAGGGAA 1320
CACCCCCACC ACGCCTGACC AGCCCTTCCT CTGTTGTGGG CTGGTGCTAG ACGTGGTAGA 1380
AACTTTCTGT TCTCCTGAAG CAGTTTGAGT TGCCTCTGCT GGACATTTGT AGTATCTCTT 1440
TCCCACCTTC TTGGTTGACT CTGCTGCTGG GAAGGGAATG ACAGGAAGCC CATGGGTCTT 1500
CTGTTGGGTG GGTGTGTTTG TGGGAAATCC TGCCATTTCA AGCCATGTGA CTGGAATTAG 1560
ATAGGATGAA GGAGGTGTGC CCTTTGGAGT GTGAGAGTCT CAAGGAGCCT GCTCTCACTG 1620
TTAGGACAGC AACCAGGCAC AACCAGGGCC ATAATGAGTG TCTCTTGGCT CAGCCCACAA 1680
AGTTATGCCT AACCATGTTT AATCAATGTT TTTTTTGGTA ATGAGAATGC ATAATAATTA 1740
TAGGGTCTGT TCACCTTTCT TTTTTACTTC CCTGCCGCTG TGAAGATACA 1790
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