| Tag | Content |
|---|
EnhancerAtlas ID | HS133-25125 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr5:60597130-60599000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr5:60598959-60598969 | TCTAATTAAA | + | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23393 | chr5:60597734-60598259 | Colon_Crypt_1 | | SE_45365 | chr5:60596282-60603394 | NHLF | | SE_46239 | chr5:60596356-60603987 | Osteoblasts | | SE_52229 | chr5:60596986-60601370 | Skeletal_Muscle_Myoblast | | SE_56302 | chr5:60596175-60599545 | u87 | | SE_63826 | chr5:60596851-60601493 | HSMM |
|
| | 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 |
| GH05I061298 | chr5 | 60593950 | 60603473 |
|
Enhancer Sequence | GTGGCCAACC TTTTATGCTG CACATTTTGG CTGTTCCCAG TTTCCCCTTT GTAGTATTGA 60
CAGGCTTTTG GAGAATAATG AAACGCTGAA ATGTTTGGCT TGGTTTCCCT CTTGGGTAGA 120
GTCTGCTGCT CAGTCTTTTC TTCTGCCTCT TTGTATCCTT TAGCTTTTGG GTGGAGGCCC 180
AGAGAGCTCC ACAAGGGGTG ATGTGTGTTT AAGAAACTCA GCTAAAGGAA ACAAACTGAT 240
TGCAAAGAAC TCTGAACCTA GGGTGTTGGG GGAAATGCTG AGCATTGTAA TTGGCCTAAT 300
GCTGCTCCTG TGAGAGATGC CATCTCCCTA GGCCTCCAAA GTTCTGGCAG GGATTTTAAC 360
TCTTCTCATC CAGCTGATGA CAGACAAATA TTCATCACTT CAACAGTTAG GTGCAACCCC 420
CAAAATGTTT CCTCAAGTCC TTCCTCACTG CAAATGCCTA CCAGCTCATC TCTGAAGATG 480
GAAAAGCAAG CGTGGTGACA TCTGCAAATC TGGACAGTGG GCTTTAGGAT TCATCTGAAA 540
AGAAAGGCTC TTGGACAGTG CTGGACCTTG CTCCCTGAGC CAGGCTGTGG GTCCAGTGGT 600
GACTCAGGAA GGAATGCCAC TGACAAGCCA CAGGCATGCC AGAGAATTAC TCAGCACAAG 660
CCAACAAGTA ACCTCATACG AGAATCAAAC GCCAGCCAAT CTGCGAACGC TTTGCGTAAC 720
AGCATATTTG GATTTGGGGC TTAGCTTTCA GGCTTGAGTT TCACGTTTGC CTGAGCATAC 780
TCCCAGCCTC CCAGGGCCCC TTCTGTGTGC CCTGCCTCTG ATTGCAAGTG CAGAGAGCAG 840
TTCTCCCAAG AGCCAGGGCT CAGCTCACCC CTGCAGGTAA CGCAGACCTC TGCTAGGGAT 900
CAGCTGTCTA TCATCTGGTG GCGCCCCTCT TTCCAGCCAG CGCTACATCT TCATATGCCT 960
TTTCTTACCA ACAGGTCAGC AATGTGGGTG ACAGATACTT CTTTTTGCTG TTGGAACACT 1020
TCATATTCAT CTCTGGTATT GTCATGGCCT TTGACATACC TTACCAACAA GAGAGGTTTG 1080
TTGACTGATG ACAGCAGGTA TAACAAAATC TAACTAGTGA CAGTTGTAAG AATTGGCAAA 1140
GTATTACTGC ATCAACAGGT ATGTGGACTG TCTAAGAGCC TCAGAAAGGA CAAAGAAAGA 1200
AGCTTACAGA TTCCGATGCC CCTTACTACT GTATCTGGCC TTTCTCCTGC CGGTATAGTG 1260
AGAGTTGACA GTTTGATGGA TTTAATTTAG GATCTATGTT AGGATGAGAT GCACTCTGTT 1320
TTCCTAAACA AATTTGCTGC AGAATGGCAG CCACAGTCTA GGGCCTCCTT GAGCTTGAGG 1380
CTAAATGACC TGATGGCCCA CCCACTTCAT CTATACTGCC TTTAATATGT CAGCATTTCC 1440
TCAAGGCCTG GGTTTCGTGC ACTCAGGGTG ATATTGAACA TGAAGTTTTC AAACAGCAAT 1500
ACCTTGGGTA ACAGACAAGG GCTAGTTAAT GATCTCATTC ATAATTCATC CCGTGAAGGA 1560
ACCATTTACA CTCAAACTCC AAGCAGGAAG AAAATATTCC CATTAGGTAG GGCTTTTTAA 1620
ATGCCTCTGC CTTTGCCACA GTGCTGAGAG AGAACTGTGG TCTTCAGTAG TAAGGGCATA 1680
TGGCTGCAAA CAGAGTGCCC AGGTTAGAGA CACCAAGAGC TGCAGCATCA CTCAGTAATA 1740
GCTATTTCAG AGGGATGTAA AGCCTTCCCT GGGAAAAAGT TGAATAGGAC TCAGTGCCTA 1800
AACACAGCAC TTTCAAAAAG AAATGAATCT CTAATTAAAC ATCCTGAAGA CAGAAGCTGA 1860
CATGTCATTG 1870
|
