| Tag | Content |
|---|
EnhancerAtlas ID | HS192-00025 |
Organism | Homo sapiens |
Tissue/cell | U2OS |
Coordinate | chr1:1004210-1007120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr1:1004737-1004751 | GTGGGGGCGTGGCC | - | 6.39 | | KLF16 | MA0741.1 | chr1:1004739-1004750 | GGGGGCGTGGC | - | 6.62 | | KLF5 | MA0599.1 | chr1:1004502-1004512 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr1:1004521-1004531 | GCCCCGCCCC | + | 6.02 | | Klf1 | MA0493.1 | chr1:1005572-1005583 | TGGGTGTGGCC | - | 6.62 | | NKX2-5 | MA0063.2 | chr1:1006876-1006886 | CTCAAGTGGT | - | 6.02 | | NRF1 | MA0506.1 | chr1:1004721-1004732 | GCGCCTGCGCG | + | 6.14 | | RFX1 | MA0509.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | + | 6.11 | | RFX1 | MA0509.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | - | 6.12 | | RFX2 | MA0600.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | + | 6.2 | | RFX2 | MA0600.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | - | 6.2 | | SP1 | MA0079.4 | chr1:1004499-1004514 | CAAGCCCCGCCCCTC | + | 6.34 | | SP2 | MA0516.2 | chr1:1004498-1004515 | GCAAGCCCCGCCCCTCA | + | 6.23 | | SP3 | MA0746.2 | chr1:1004738-1004751 | TGGGGGCGTGGCC | - | 6.57 | | SP4 | MA0685.1 | chr1:1004499-1004516 | CAAGCCCCGCCCCTCAT | + | 6.24 | | SP8 | MA0747.1 | chr1:1004738-1004750 | TGGGGGCGTGGC | - | 6.11 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_24070 | chr1:1002554-1005867 | Colon_Crypt_2 | | SE_24817 | chr1:1002490-1006081 | Colon_Crypt_3 | | SE_27529 | chr1:1001798-1011077 | Esophagus | | SE_34539 | chr1:1004454-1006480 | HCT-116 | | SE_41944 | chr1:1001963-1005965 | LNCaP | | SE_58139 | chr1:1004236-1004768 | VACO_9m | | SE_58139 | chr1:1004812-1005267 | VACO_9m | | SE_65935 | chr1:1001682-1006445 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1005293 | 1005547 | | chr1 | 1006044 | 1006328 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001066 | chr1 | 1001837 | 1006486 |
|
Enhancer Sequence | CGGGACGACG AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT 60
CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT 120
CGTGATTGAC ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC 180
CCCCCGCCCT GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC 240
CCACCCCTCA GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC 300
CCTCATCAGC AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC 360
AAGCGCGCTT GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG 420
TTTGGCGGCA GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG 480
CGCTGCAGCG GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC 540
CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG 600
CGAGCCGCCT CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG 660
CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC 720
CTCTGGGAGG GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC 780
CCCGCAGCCC TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG 840
CAGGGAACCC CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT 900
CCAGGACAGA GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC 960
GACAGGCTGC GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC 1020
ACTCCGTGCG GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG 1080
TCTGGGATGT GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA 1140
GTGAGGTGTG TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC 1200
CGATGACAAG GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG 1260
CTGTGACCCG TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT 1320
GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG 1380
CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC 1440
TGGTTGGAGC AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG 1500
CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT 1560
GGGGCTGATG ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT 1620
AGCTGACCTC TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG 1680
ATCTGCAGGC TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT 1740
CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG 1800
GCCTAGTATG GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG 1860
GCTCTGAACC AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG 1920
GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC 1980
CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC TTGGGCCCAC 2040
CTGTCCCAGT GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA 2100
GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC CAAAGATGGA TACAAATAAT TTATTTTAAA 2160
AGGTACAATT CACAAGGTTG GAGGGGTAGC TGGAAGTTTC TGTGGTTACC TTGCACTGGG 2220
GGGCTGCCCT GCCTCCACTC TCTCCCCACA GTCCGAGGGC AAGATGAGCA CCCCCACCCA 2280
ATGGCAGGAC CAGCCCTGCG GGGAAATGTC AGCATGAGTG GAAGCACGGC AAGGCCCCTT 2340
CCTTCTTGGC AAGGGGCTTC CCTGGCAGGC AGTTCACAGG GTGTGTGGGT GGGGGGGATG 2400
CTGACCAGCT GCTCTCCTGG ACCCTTCCTG TACGAGCCTG TTTTTTTTTG TTTTGTTTTG 2460
AGACAGGGTC TCCCTCTGTC GCCCAGGCTG GATGCAGTGG TGCAATCTTG GCTCACTGCC 2520
ACCTCCACCT CCCCGGTTCA AGCAGTTCTC CTGCCTCAGC CTCCCCAGTA GCTAAGAGGC 2580
ACCCACCACG ATGCCCGGTT AATTTTTGTA TTTTTAGTAG AGATGGGGTT TCACCATGTT 2640
GGCCAGGCTG GTGTCAAAAT CCCGACCTCA AGTGGTCTTT CTGCCTCAGC CCTCCAGAGT 2700
GCTGAGATGA CAGGCGTGAG CCACCGCGCC CGGTGAGACT GTGGTTCTTG GAGGCTTTGG 2760
GGATCCTCTT GTCCACCCCG TCAGGACCCA GCCTGGAGAA TGAGGGGTGG ACAAGCTAAA 2820
TGGAGCCTGG TCTTGGTGGG GCCCCGGTGG AGTCCTCAGA GATGCCAGGC TCCTTTCGCG 2880
TCCTCGGGGA CCGACTTCCA GTGGCTGCTG 2910
|
