| Tag | Content |
|---|
EnhancerAtlas ID | HS053-01121 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:39623670-39626710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr1:39624486-39624498 | GGTGACGTCACT | + | 6.22 | | CREB1 | MA0018.3 | chr1:39624486-39624498 | GGTGACGTCACT | - | 6.22 | | Foxq1 | MA0040.1 | chr1:39624109-39624120 | TATTGTTTATT | + | 6.62 | | Hnf4a | MA0114.3 | chr1:39624505-39624521 | GTGGTCAAAGTCCAGT | + | 6.51 | | KLF4 | MA0039.3 | chr1:39625567-39625578 | ACAGGGTGTGG | - | 6.14 | | Nkx3-2 | MA0122.3 | chr1:39625399-39625412 | AATAAGTGGTTTT | - | 6.14 | | ZNF263 | MA0528.1 | chr1:39625134-39625155 | TGGGGAGGAGGGTGGAGGGAG | + | 6.03 | | ZNF263 | MA0528.1 | chr1:39625137-39625158 | GGAGGAGGGTGGAGGGAGGAA | + | 7.19 |
|
| | Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
| SE_02052 | chr1:39623700-39625273 | Aorta | | SE_06399 | chr1:39623194-39625443 | Brain_Hippocampus_Middle | | SE_08441 | chr1:39623554-39625364 | Brain_Inferior_Temporal_Lobe | | SE_14598 | chr1:39623413-39625353 | CD4_Memory_Primary_7pool | | SE_25799 | chr1:39623252-39625649 | Duodenum_Smooth_Muscle | | SE_30410 | chr1:39623509-39626362 | Fetal_Muscle | | SE_32006 | chr1:39623632-39626196 | Gastric | | SE_35822 | chr1:39623459-39627010 | HMEC | | SE_36947 | chr1:39622990-39632657 | HSMMtube | | SE_37973 | chr1:39623508-39626483 | HUVEC | | SE_42256 | chr1:39623665-39625283 | Lung | | SE_42256 | chr1:39625384-39626180 | Lung | | SE_45768 | chr1:39623568-39627263 | Osteoblasts | | SE_47164 | chr1:39622875-39627546 | Panc1 | | SE_51765 | chr1:39623560-39625373 | Skeletal_Muscle_Myoblast | | SE_53123 | chr1:39623552-39625824 | Small_Intestine | | SE_54583 | chr1:39623552-39625585 | Stomach_Smooth_Muscle | | SE_63563 | chr1:39623442-39625404 | HSMM | | SE_64261 | chr1:39623623-39625416 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr1 | 39623945 | 39625358 | | chr1 | 39626499 | 39626706 | | chr1 | 39626344 | 39626656 | | chr1 | 39623773 | 39626200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I039157 | chr1 | 39622978 | 39627255 |
|
Enhancer Sequence | TAATGCAGAT GAGCCATTTT GAGTTCCTTA CAACAAAGAT GCTGTGGAAA TTTCAGGATT 60
TTCCCCCTTT AGTTATAATA TGGGTAGCTT ATCCTAAGAA CCTGTGACTA TTGGGATGGT 120
CATCTTTTTG AGGCCAGCAG TAGAAAGAAA TTTGCAGTAG TGACTGACAC ATTAAAGCAA 180
CCCCGAAACA AATCAGAGTG AAATAGTGTC CTGGAGTTGG GGATATGTGG GTGATATCTG 240
GGCTGCATTT TCTCTCTAGG TATCCATGGA GAGGGTCCTG TCTCCCTGAA TGGTTGTGCT 300
TTCAACAGTT AGGGAATGAG CTTGACAGTT TCTGCTTCTT CCCTCCCCTT GCCTTGAACT 360
GCCTTGATAT GCAGTGCCTC CTCTGTTGTG TGGCTGTATT CCAGTCCGTA AACATGACTG 420
CTGTAAGGAG AGTACAGAGT ATTGTTTATT TTGTAAAACT TGTCTCATTG CCATGTAATA 480
TTTGCTCAAG AGCTCCTGTT GTGGTGATAT TCTTGTGGTG AGCATGGCCC TTTAAAGATT 540
TTGTTCTCAA ATGTTAAATG AGCCCCTGAC TGGTGTCCTG AAAAGCATTT AAGCTTCTCT 600
CCCTAGAGTT TAAGCAAGAG GAGCAGTAAT CCCAGTGGAG CCTGGGCTGG GGTCTAGAGA 660
GAAGGTGGCA GATGAGGTGG CAGATGACAG GCAGGGGCGG TTGTGGTCCC GTAGCTCATT 720
TGCACAAAGG AGGGGCTGGC CTCTCCTGGG GAGGTATTTC CGCTCACTGG AACAAATGAG 780
GGCGCTCAAA AGGCTGTAAT GTAATGAGGC TTCTCTGGTG ACGTCACTTG TAAATGTGGT 840
CAAAGTCCAG TTCTTGGGGG CTAGTAGAAG CGGGAGTAGA GATCATTCGG TTTGCATGCT 900
TTCACTTCTC AGCTGTCACT GTGCCATGGT GCCTACTTTC AGCCAGTGAA CCAACTCAAC 960
TGGGCCGGGC ATGAACGCTT ACAAGTATCA GAAGTTCCTG GAGGGACTCA ACAACCTTAG 1020
AGGTATTACA AGGCTTCAGG CTCCCTACCC TTTGTCCTTG CTGATCGTGT GAGCACTTAT 1080
TATGGTGTGT ATTGTATAGG GTCTGTAAAA CCCTCCTGCT CTGAGCTGGC CCTATTTTTT 1140
ATGCGTTTAG GCAATTAAAC AGAAGGGATA GAGTTTGTAA ATGCAATCCT AAGTGAGTAG 1200
GAGAGAATCT CCTTAGGTAC TTCAGCAACA GCCTGTTGTC TTGCTTGAAC GGACAAGTAA 1260
GAAATGTCCC CTGTATTCTT GAGCTCAGAG GGCTCAGGGC ACTCCCTGTT TTCTTTGAGG 1320
TGGCCAGACA GTGTGGGTGG AGGGCTCTTG CCATAGGGCC CTGCAGCCTC ACCTAGGTGT 1380
AGTTATGTTT CTTGGGCCAG GTTTTCCAGT TGCTTGTGTC TACAGTGAGT CAGAGTCCCA 1440
TTTGGAGAGA ACTGGAGTTG GGAGTGGGGA GGAGGGTGGA GGGAGGAATG CAGGTTGATG 1500
GGCTATTTGT AAGCCCATTG TAAAGTAAGC CTTTGTAAAG AGTAAAACAA TGACTTTGAA 1560
AGAGGAAGCT TTTTATTAAA GTTTTAAAGG AAATAGTGTT TTCTTTGCAT CATGGGCAAA 1620
TTCTTCACTG ACCAGACATG AGAAGAATGT ACTCAGATGT GATGTAGGAC TCTTTTTGGA 1680
TATTAAAGAG AAAAATGAAT GAAATCTTTT TACTTTCCCT TCTCTAATTA ATAAGTGGTT 1740
TTATTTCCAT TTGCAGAGGA GGGTGCTTAA ACCATTTTTC TTTCATCAGT AGTTAGGATT 1800
CTGGACCCAG AGCAACCATG GGGTGTGGAG AGAGTGGGAG GGGGTAGAGG GAGGAAAGGA 1860
GTAAACTGGG TTTTTTCAGG GATGAGGAAA GTGGCAGACA GGGTGTGGGC AGGAGATCTG 1920
TACTCCCTTC TTGCCAGGGT ATGTAGATGT TTTACTTTCT TTCACTATCT GTTGAAGAAC 1980
TCTGGTTCTA AGAAATATAT ATGGAGAGCT TTGTATGCTA TAAAGGGATA TACAGGTCGG 2040
GCATGGTGGC TCGCACTCGT AATCCCAACA CTTTGGGAGG CTGAGATGGG AGGATCGCTT 2100
GAACCCAGGA GTTCTAGACC AGCCTGGGCA ACATAATGAG ACCCCCATCT CTACAGAAAT 2160
GTTAAAAAAT TAGCTGGGCA TGGTGATATG CACCTGTACC CTTAACTACT TGGGAAGCTG 2220
AGGTGGAAGG ATCACTCTGA GTTCATCTTA GAGGTACAGA ACCCAAATAA CACAGCAAAG 2280
AGCCCCAGAG TCTGGAGTGA GAAGAGTGCT GCTCTCTGGT GCTAGAGACC ATGTGAAGAA 2340
GGGAAGAATA CCCACATCTG ACTAAGCATA TGTGTAAATG CACCTTCCTC TCTGAGACAA 2400
AGAGCTGTAG TATGGGGCTT TAGAGTGAAG GTAATAGATC TTTTCTCTCC ACACTACTAC 2460
TCACCTTGAA TGGAGTTCTG TTTTCTAATC TTTCATTCAC TATTGTTTGC TTCATTCACT 2520
TATATACACT GTATAATAGT CTTTATAGCA TAAAACATAC AATATATAGC AGTTTCTCTT 2580
GTTGACCCAA AGAAAGGATC AGATTTAAAC TCTTCTTTGC TCCTGCAACC TGAGTCTTTT 2640
TCAGGTGGGA GAAGTTCCTG GAAAGAGGAC ATGTAGTTTT TTTGGTTTAG TCCTTATCAT 2700
TTTTTGGAAT GTTGCTATAG GTCTTAGACA ACTATTCCCC CAATTCTGGG CTGCCAGGCA 2760
GAGAGTTAGA TACAAACCAT TGCCTTTGTC AAATCCTCCT GTGGGTTGAG TTTCACCCAC 2820
TGTGCCCCCT GATTAAGGTG AATGGTTACT TCCCTTCTTC TTTTCACTTA ATATCTTTGT 2880
GTATTCCAGA AGGGCTGATG GAAAGAGGTA ATTGGCTCCC CTCTTCATTT AGTTACTGAC 2940
TGTTGCTTTT CTTGGCATGG TTCAGCTTGT AGACATTCCT CCATCTAGTG GGTAACTGTT 3000
GAAGGGAATC CAGTGGGAGA ATAGAGACAT TGTACAAGTT 3040
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