| Tag | Content |
|---|
EnhancerAtlas ID | HS145-01586 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr1:151960860-151963310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:151963075-151963085 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr1:151963075-151963085 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr1:151963075-151963085 | ATTTTCCATT | + | 6.02 | | REST | MA0138.2 | chr1:151963182-151963203 | AAAGCTCTCCATGGTGCTTGC | - | 6.59 | | TEAD1 | MA0090.2 | chr1:151962716-151962726 | CACATTCCAT | + | 6.02 | | ZNF263 | MA0528.1 | chr1:151961795-151961816 | CTTCCCCTCCCCTCCTCCCCC | - | 7.84 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00284 | chr1:151951696-151968835 | Adipose_Nuclei | | SE_02826 | chr1:151960179-151963618 | Astrocytes | | SE_09689 | chr1:151958965-151967354 | CD14 | | SE_23217 | chr1:151961002-151967250 | Colon_Crypt_1 | | SE_24041 | chr1:151961119-151961502 | Colon_Crypt_2 | | SE_24041 | chr1:151961532-151962451 | Colon_Crypt_2 | | SE_24041 | chr1:151962505-151962780 | Colon_Crypt_2 | | SE_25129 | chr1:151961024-151962388 | Colon_Crypt_3 | | SE_26790 | chr1:151960243-151968142 | Esophagus | | SE_27992 | chr1:151959711-151968123 | Fetal_Intestine | | SE_28908 | chr1:151959611-151968309 | Fetal_Intestine_Large | | SE_33866 | chr1:151960207-151967313 | HCC1954 | | SE_34778 | chr1:151959926-151968552 | HeLa | | SE_35880 | chr1:151959933-151975921 | HMEC | | SE_43050 | chr1:151960740-151967310 | Lung | | SE_44654 | chr1:151960194-151968465 | NHDF-Ad | | SE_45267 | chr1:151960456-151967435 | NHLF | | SE_47215 | chr1:151938610-151969225 | Panc1 | | SE_50609 | chr1:151960617-151968225 | Sigmoid_Colon | | SE_52876 | chr1:151960623-151968189 | Small_Intestine | | SE_56104 | chr1:151960357-151967571 | u87 | | SE_57650 | chr1:151961137-151963029 | VACO_503 | | SE_58076 | chr1:151961586-151962069 | VACO_9m | | SE_58076 | chr1:151962098-151962413 | VACO_9m | | SE_58076 | chr1:151962967-151963306 | VACO_9m | | SE_64176 | chr1:151960195-151967437 | HSMM | | SE_64341 | chr1:151960135-151968569 | NHEK | | SE_67706 | chr1:151960357-151967571 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 151960875 | 151961433 | | chr1 | 151961675 | 151962369 | | chr1 | 151962584 | 151962808 |
|
Enhancer Sequence | GAAGAGCTCT AATGGGAACC TGAGACATGC TTTGGTCTGG TTCCTATCTC TGAGAGATGC 60
CTGTTCAACA CTGATTCTCA AATGCTATCT TTTACAGAGG AGAAGGTGGA GTGGGTAAAC 120
ATGAGGATTG AGCAATTAAC ACTTAAGAAT TGTAAATTCT ACCCCTTAAT CTCCAGAAAA 180
GTATGGGAAC CAGCAGGCCA AAGAATGCTA TAAATCAGAA TCTGGCATGA GTCATCTGAA 240
AGGCAGTTAG TTATCTTGGA GAGAGCTGCA AATTAATGCT TCAAGGTCTG CTGTGAGATG 300
AATTCCAGGG GAACCACACC CTTTTCCTTC TCTTCTGACA CAGCTCAGAT CTGGCTCATC 360
CCCCATCCCT CATATGGGTT TCAGATGGCA GTGGGCTTAC AGAGAGTCTG CCTTGCCTGG 420
ACTGGTACTC CAAGTCCAGC AATTTAAGAG AACTGAACTG GGCGAGTCAC CTCTGGGAGA 480
AGGACGTGGG ATCCCACCCC AGTTCTTAAA TAACTCAGGA AAGGAGTCAG ACACCACAGA 540
GGTTTAAAAA TACCTGTGCT CAAGTTCAGA GCAGCAGAGC ACTTCAGGAT CAATTCCCAA 600
AGATCCCAGA AATTGGAACT GGGTGGGGTA CCTAGTTTAC TTTTTTCAGA TGACAGGACA 660
GAAGGAAAGT GCAGAATTAA GAAAGGGAAT GCAGCAGGGT AAGGACCTCT AAATTTTAAA 720
AAGGCTAATT TTAGGAGGTT CTAAGAAATA CAAGTTGTCA GCTGAGGAAA TCCTGGCCAC 780
CCTTGAGTAT CTTCTTCAGG AGAGCAAGGT GAGTCTACCT CACACTGTGT GAGTGCTTAG 840
GTCTGAAGTC ACTCAGTCGC ATGCCTCTCT TGCCCACAGC CATTACGAAG TGACGGAGCT 900
TCCTTCTCTG AAGTTACATC CTTCTCCCAC TTGGTCTTCC CCTCCCCTCC TCCCCCAGCG 960
GTTTTATTCA GTGGATGGAT TGTGAATATT GCAGCCAGCT GACTCCCTGT GTGTCCAGTA 1020
GGCCTTCTGC AATAAGGATG CAGAGGAGGG AGTAGCCAGG AGGTGAAAAT AGCATTGAAA 1080
ATCAGTGGAG AAGCCCTTGT CTCCTCAGCA ACCAGTACCC CAAAGGGCAC TGACCAGGGC 1140
CACAGCAAGG AACTCTGTTT TGGGGAAGGA GTTGCACACT GGCTTTAAAA TAAGACAAAG 1200
GAAAGGGGGA AATGTTGTGA TTAAAACTCT GTTCTCTTGG CTAGAGGATG AATCATGTAA 1260
CTCTTGTCTG AGTGCAGCCA ATGGTTGCCC AACTGAGTCA GCCCTGCCTG GCCCTCCGTT 1320
CTTGGGTGGG GCTTGCCTGG GCAGGGCTGT CTGCAGCACT GCTAGCTGCC AAAACTGAAG 1380
TTCTTCAGGG ACTTCAATCT GGCATTTCCA CCCTCACGTA GCCACTCTGC AAGCTCTATT 1440
CCTGGACAGA TGTGGGCTTC CTGCATCCTG GTTAGACACA TTTTGACAGG AGGGCCTTGG 1500
GGCTGGGGCT GAGGGGCTGC AGTGTCCTCT CTATCCCCAA TAACGTACTC TTGCACCTGA 1560
AACATTCAAT TTCATTTAAT TGTTTACTTG TCTGCCTGAG ATTTAAGCTT CTCTTGATTA 1620
AGAACTACAA ATTATTCTGC TTTTATTCAT GGAGCACTAT ATAACTGTTA TGTGCATAAA 1680
TGAACCACAC AATCCCTTGG GCAGTAGCTG AGGTGCAGGT GTGATTACCC AGGACTAGGC 1740
TGAAAGCCTT GTAGCTCAGA GCTCAGGAGG ACGATGTGAG AGCTGGGAAG GGCCAGGAAA 1800
GGGGCCCCAA AAGTGTTCAA CTATGAACGG AACAGTAGAT AGAGTACACA GGAGTGCACA 1860
TTCCATACGC AAAAGGAAAA ATATGTGTCC TGCTAAACAG GTCTAGTCAG AATGACATGA 1920
CTGTGCTCCT TCTCTTCTAA CACTTGCTAT TTTCTCGTGT TTCATTCATC CCATCTTCTA 1980
CTTTTTGCTT TTCTAGTGCT GCTATCTCAC TGCTGAGCTC CACAGGATAA TAACAGCCTT 2040
GCTGTCCACT CACCTTTTAT TGAAGTATTC TAATCTGATG CCTATACATG CCCTCTACAT 2100
GTTTGTCTGA GCAACAGGTC TTAAGAAGGG AGGCGGAGAC ATCTTTCTCT GCATAGTTTT 2160
CTCTATGGAA AACAATTCTG GACTCCACAA ATTTAGTTAC CTTAGGAGGA ATTCAATTTT 2220
CCATTTTTGG TTCTCCCTCC CTGAGCACCT ACTTTGAATG TCCCAGACAT GGTGTTAGGC 2280
ATGAGGGTGT TCACACACAC ATACACACAT GCACACACAC ACAAAGCTCT CCATGGTGCT 2340
TGCCTTTGAG GAGTTCACCA GCTAATGGAA TACTATTAAA GCATTTGGCC TGAATTCTAG 2400
TTATTTGTGT TTCTGTTTCT TTCCTCACTA GGTTGCAGGT TTTTTGAGCA 2450
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