| Tag | Content |
|---|
EnhancerAtlas ID | HS108-03799 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:202074170-202076930 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:202076050-202076061 | ACAGGGTGTGG | - | 6.14 | | KLF5 | MA0599.1 | chr1:202076522-202076532 | GCCCCGCCCC | + | 6.02 | | ZNF263 | MA0528.1 | chr1:202076060-202076081 | GAAGGAGGGGTTGGAGTGGGA | + | 6.1 | | ZNF263 | MA0528.1 | chr1:202075446-202075467 | GGAGGATCGGGGGGTGGGGGG | + | 6.72 | | ZNF263 | MA0528.1 | chr1:202076784-202076805 | GGAGGAGGAGGATGGGGAAAT | + | 7.16 | | Zfx | MA0146.2 | chr1:202074491-202074505 | CCCGCCTCGGCCTC | + | 6.01 | | Zfx | MA0146.2 | chr1:202076012-202076026 | CAGGCCTAGGCCCA | - | 6.22 |
|
| | Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
| SE_23058 | chr1:202074351-202079442 | Colon_Crypt_1 | | SE_23723 | chr1:202074370-202077777 | Colon_Crypt_2 | | SE_24689 | chr1:202074418-202077795 | Colon_Crypt_3 | | SE_27253 | chr1:202074329-202078395 | Esophagus | | SE_27872 | chr1:202072821-202079531 | Fetal_Intestine | | SE_28794 | chr1:202072812-202079552 | Fetal_Intestine_Large | | SE_32199 | chr1:202074329-202079443 | Gastric | | SE_33417 | chr1:202074259-202079545 | H2171 | | SE_34936 | chr1:202073327-202079210 | HeLa | | SE_47709 | chr1:202074443-202079432 | Pancreas | | SE_50637 | chr1:202074313-202079465 | Sigmoid_Colon | | SE_52669 | chr1:202074270-202079462 | Small_Intestine | | SE_57667 | chr1:202074454-202077840 | VACO_503 | | SE_58006 | chr1:202075045-202075484 | VACO_9m | | SE_58006 | chr1:202075707-202076107 | VACO_9m | | SE_65583 | chr1:202074401-202078965 | Pancreatic_islets | | SE_67005 | chr1:202074259-202079545 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 202074201 | 202075946 | | chr1 | 202075010 | 202075191 | | chr1 | 202076459 | 202076551 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I202103 | chr1 | 202072772 | 202079378 |
|
Enhancer Sequence | AAACTCCCAA CCTAAAGTGA TGCATGCACC TTGGCCTCCC AAAGTGCTGG GATTACAAGC 60
GTGAGCCACC GCACGCAGTC TTTTTTTTTT TTTTTTGAGA TAGAGTCTAG GTCTGTCGCC 120
CAGGCTGGAG TGCAGTGGTG TGATCTCAGC TCACTGCAAC CTCTGCCTTC TGGGTTCAAG 180
TGAGTCTCAT GCCTCAGCCT CCTGAGTAGC TGGAATTACA GCTGCACGCC ACCATGCCCA 240
GCTAATTTTT GTATTTTTAT AGAGTCAGGG TGTCACCATG TTGGCCAGGC TGGTCTCAGA 300
CTCCTGACTT CAAGTGATCT GCCCGCCTCG GCCTCCCAAA GTGCTGGGAT TATGGGTGTG 360
AGCAACCACA CCCGGTGGAG TTCTCTTCTA TAATATTTAT ACTTCATCTT TCAAAAATTG 420
AGCCCATATT GCTGCATGCC AAGCATTGTG TGCCCGAGTG ATGCACAGGT CACTTCATTT 480
AATCTTCACA ACAATCCTGT GAGATAGGTA ACCTCATGCC CAAATTACAG AAGAGGCTCT 540
GTGAGGTCAG AAACTGGCCC AGGTCTCACA GCTGACTAGT GAGGAGCTGA GATTTGCTAG 600
GATGACCTGA CACTCTGAAT TCTCTAAATT CCACCTCCTT AACACAATAC ATGTAGTCAG 660
GGAAGGCCTG ACTTTATATT ATTCATTGGC CCCGAGAGCT GACTCAGACT CCTGTGGCAG 720
CCCCAGGAGT CCTGGGTTTC AGAGGGAGTG GGAGGTGGGC AGCAGAGGGG CCCTCGAGTT 780
TCGATAACCC CCCTGCACTT AGGCTACAGG CTGCATTGTA TGATAGCGAC AGACCCAGAC 840
CAGAATCCCT TCACCCTCCT CTCTAGGGTG GAGCCCCTTC CAGCAAAGCT GGCCCAGCCC 900
TGTGATGTCA CACCACTGGG CAGGGCTTCT GGGGATTGGT GACACCCAGC TGACGTCAGG 960
GAGGTGGAGA AGCCGCAGGT CCCTCTTATC CCCAGGGCAG TTCAGGGGCT TGACTGCATT 1020
TTAGCGATGA TTGTAGTTAC AGATTGCTCT CCGAAACACT GGGCAGGAAA AGCTTGCTGG 1080
TGTTCTGCTT TTGGCTCTGG GATTTGAACC CATGACTGGC TCAGGAGACT TGAGATTACC 1140
AACGTGCTTT GTGTCCCCAA CAAGTCACTT GTCCTCTCTG GGCCATCTCT AGAGCACAGC 1200
CTCCTAATTC AATAAAATGA AGAGGCTGGA GGAGAGATTG CCAAGGACTC TTTCAAGAGG 1260
CCCAGATAGG AGAGCAGGAG GATCGGGGGG TGGGGGGGTG TTCTGAGTTG GCCCTGTCAT 1320
GGCCCTAATC TGTCCTTCCC CCATCCTTCA CTCCCCCTCT TATCCCTGGT GGCCCCGGAG 1380
TGAGAACGTG ACTCATCCAG CTCCAGGCAC CCAGTTTCAG CCTTGCCCCA CCCCTGCCCC 1440
GGGCCTCTCA TTTGCTGTTT ACCCCCCAGG AGCAGGTGCA CCTGGGTCAC CTCACCGCAG 1500
GAAGGAGAGA TATAAGGCTC TAGGGCACAG CCTGACTCCA CACCCACAGA TTGCCCAAGG 1560
CCAGCACAGG GGTTGGAGCT CTCTAGAAAG GTGAGGCACT TGGGGAGCAT AAAACAGCTC 1620
CAAGTGGGCC CACCACCCTG TCCAGCTGCT GAGCTCAGCC CGCTGCCTCT CATCTCTTCC 1680
CATGGGTTTG TCTTCATTCA CCCACTGCCC CTAGAGCAGC CCAGGCCCCG CCCTCAGCCT 1740
GAGGACCCTG TGCAGAGCTC AGCCAGTTCC AGGAGGGGAG GGCCTCTTGA AGGCAGTCGG 1800
GGGCCAGGGG AGCTGGTGCT CACATTGAGG AGCTGTGGAA GGCAGGCCTA GGCCCACACA 1860
TCCTGTGCTA AGAAGAGAGG ACAGGGTGTG GAAGGAGGGG TTGGAGTGGG AGACCCATAG 1920
CCTGATTCAG CCCCGAATGG AAAAGTGAAG TTATGGGGGG ACTGAAAGGT TTGGTGACAG 1980
ATACTGGGAT GTGAGTCTGG AAAGCGGCTT TGAGTCATGG CTTGGCATCT ACCCTCCCTT 2040
TGTGACCTTG GCCATGTCCA TTGCCCTCTT ATCCCCATCT GTACAAGGCA GGCGCCTCAG 2100
TGTTCCCATC TGTACAAGGT AGGGGCTCAG CTGGATAAGC CTAGGCTCCT TCTAACCCTG 2160
GCACTCTGTG GTTACCCAGG TGGGCATCCC CACCCCAGTG CCCAACCTTC CCCTATCCCC 2220
ACTAGCTCCC GCATCTCCCC CATGGAGAAA AAGAAACCTC GCTGGGTCAT GGAACATGGG 2280
AAGGGTTGGC AATTCCTGTG TGAGGCAGCC CAAGGCAACC TCGGAGCCCT CCTGCAGATA 2340
CCCAGGGGGC CTGCCCCGCC CCTGGCCCAG GCTCCAGACC ACAGAGCAGA CAACAAAGGC 2400
AGGCAGGTGG AAAATTCCCT CTGGCTCTCC GCCCAGGCAC CCTGGATGGC AACTGTGCCA 2460
GCCTGGGCGG GCAAGAGCCG GGAGTCCAGG ATACCAACAG GCAGCCTGGC AGCCCCAGGG 2520
AGCTGATAAG GGGCCTGTCA AGGTCTCCCC AGTTCAATTG CCCCCCACTG CTCAGACACA 2580
GAAATTGTAT TCTACTCAGG TGGACAAACA GGTGGGAGGA GGAGGATGGG GAAATATGTG 2640
GTTGTTTGAA CTTCTCAGAA GTTGTAGCCC TGAGCCAAGA AGATTATGCC AACTCCTCCC 2700
ACTACCCTGA GCTGAGTGGT CCCTGGGACT CTTAATGGAG GACCGGGGGC TGCAGCTAGT 2760
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