| Tag | Content |
|---|
EnhancerAtlas ID | HS184-00009 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:1003660-1006200 |
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 | | KLF5 | MA0599.1 | chr1:1004157-1004167 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr1:1004196-1004206 | GGGGCGGGGC | - | 6.02 | | Klf1 | MA0493.1 | chr1:1005572-1005583 | TGGGTGTGGCC | - | 6.62 | | 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 | | ZNF263 | MA0528.1 | chr1:1003831-1003852 | CCTTCCTCCTCCTCCTGCTCG | - | 6.88 | | ZNF263 | MA0528.1 | chr1:1003819-1003840 | CCCTCCCCATTTCCTTCCTCC | - | 6.89 | | ZNF263 | MA0528.1 | chr1:1003825-1003846 | CCATTTCCTTCCTCCTCCTCC | - | 7.03 | | ZNF263 | MA0528.1 | chr1:1003822-1003843 | TCCCCATTTCCTTCCTCCTCC | - | 8.3 |
|
| | Number of super-enhancer constituents: 10 | 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 | chr1:1002321-1004360 | HCT-116 | | SE_34539 | chr1:1004454-1006480 | HCT-116 | | SE_41944 | chr1:1001963-1005965 | LNCaP | | SE_58139 | chr1:1003761-1004209 | VACO_9m | | 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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001066 | chr1 | 1001837 | 1006486 |
|
Enhancer Sequence | CCCCGCCCAG TGTGTGTGGG GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT 60
TTCCTTATAA AATAACTGTC CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT 120
TCCCCAGGCA CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC 180
TCCTCCTGCT CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT 240
GTGCCTCAGC CTCCTCCTCC CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG 300
AGCCACAGCG TACGGTGCAG CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG 360
CCGATCCCGC CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC 420
CGCGGGCCGG GCCCATGGTG GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT 480
GCAGATGCAG GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG 540
CGGGGCCACG CGGGACGACG AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC 600
GCCCCCCACT CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG 660
GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC 720
ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT 780
CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC 840
AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA 900
GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG 960
ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC 1020
ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG 1080
GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT 1140
CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT 1200
AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG 1260
GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG 1320
CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC 1380
TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC 1440
GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG 1500
CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC 1560
CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT 1620
GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA 1680
TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC 1740
CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG 1800
AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG 1860
GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG 1920
GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA 1980
GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG 2040
AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG 2100
CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA 2160
TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA 2220
GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG 2280
GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC 2340
TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT 2400
CAGCCCCCGG GCTCTGAACC AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA 2460
AGTGTCCTGG GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA 2520
CTCCAGAAAC CCCCAGCCTG 2540
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