| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01833 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:39623360-39626090 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I039157 | chr1 | 39622978 | 39627255 |
|
Enhancer Sequence | TTACTTAACC TCTGTCTATT TACTTTTTCT TTTTTTGAGA CAGGGCCTCA CTTTGTCACC 60
AAGGCTAGAG TGCAGTGGTG TGATCTTGGC TCACTGCAGC CTCAACTTCC CAGGTTCAAG 120
CGATCCTTCA TCCTCAGCTC CCCAAGTAGC TGGGACTGCA GGAACGTACC ACCACACCCA 180
GCTAATTTTT TGGAGTTTTT GTAGAGACGG GGTTTTGCCA TGTTGCTCAG GCTGGACTTC 240
TGTCTGTTTT CTCATCTGAT AATGAAAAGT TGCAATTATT TTCACAAGAT ACTTTCAAAG 300
ATGAGTCTAA TAATGCAGAT GAGCCATTTT GAGTTCCTTA CAACAAAGAT GCTGTGGAAA 360
TTTCAGGATT TTCCCCCTTT AGTTATAATA TGGGTAGCTT ATCCTAAGAA CCTGTGACTA 420
TTGGGATGGT CATCTTTTTG AGGCCAGCAG TAGAAAGAAA TTTGCAGTAG TGACTGACAC 480
ATTAAAGCAA CCCCGAAACA AATCAGAGTG AAATAGTGTC CTGGAGTTGG GGATATGTGG 540
GTGATATCTG GGCTGCATTT TCTCTCTAGG TATCCATGGA GAGGGTCCTG TCTCCCTGAA 600
TGGTTGTGCT TTCAACAGTT AGGGAATGAG CTTGACAGTT TCTGCTTCTT CCCTCCCCTT 660
GCCTTGAACT GCCTTGATAT GCAGTGCCTC CTCTGTTGTG TGGCTGTATT CCAGTCCGTA 720
AACATGACTG CTGTAAGGAG AGTACAGAGT ATTGTTTATT TTGTAAAACT TGTCTCATTG 780
CCATGTAATA TTTGCTCAAG AGCTCCTGTT GTGGTGATAT TCTTGTGGTG AGCATGGCCC 840
TTTAAAGATT TTGTTCTCAA ATGTTAAATG AGCCCCTGAC TGGTGTCCTG AAAAGCATTT 900
AAGCTTCTCT CCCTAGAGTT TAAGCAAGAG GAGCAGTAAT CCCAGTGGAG CCTGGGCTGG 960
GGTCTAGAGA GAAGGTGGCA GATGAGGTGG CAGATGACAG GCAGGGGCGG TTGTGGTCCC 1020
GTAGCTCATT TGCACAAAGG AGGGGCTGGC CTCTCCTGGG GAGGTATTTC CGCTCACTGG 1080
AACAAATGAG GGCGCTCAAA AGGCTGTAAT GTAATGAGGC TTCTCTGGTG ACGTCACTTG 1140
TAAATGTGGT CAAAGTCCAG TTCTTGGGGG CTAGTAGAAG CGGGAGTAGA GATCATTCGG 1200
TTTGCATGCT TTCACTTCTC AGCTGTCACT GTGCCATGGT GCCTACTTTC AGCCAGTGAA 1260
CCAACTCAAC TGGGCCGGGC ATGAACGCTT ACAAGTATCA GAAGTTCCTG GAGGGACTCA 1320
ACAACCTTAG AGGTATTACA AGGCTTCAGG CTCCCTACCC TTTGTCCTTG CTGATCGTGT 1380
GAGCACTTAT TATGGTGTGT ATTGTATAGG GTCTGTAAAA CCCTCCTGCT CTGAGCTGGC 1440
CCTATTTTTT ATGCGTTTAG GCAATTAAAC AGAAGGGATA GAGTTTGTAA ATGCAATCCT 1500
AAGTGAGTAG GAGAGAATCT CCTTAGGTAC TTCAGCAACA GCCTGTTGTC TTGCTTGAAC 1560
GGACAAGTAA GAAATGTCCC CTGTATTCTT GAGCTCAGAG GGCTCAGGGC ACTCCCTGTT 1620
TTCTTTGAGG TGGCCAGACA GTGTGGGTGG AGGGCTCTTG CCATAGGGCC CTGCAGCCTC 1680
ACCTAGGTGT AGTTATGTTT CTTGGGCCAG GTTTTCCAGT TGCTTGTGTC TACAGTGAGT 1740
CAGAGTCCCA TTTGGAGAGA ACTGGAGTTG GGAGTGGGGA GGAGGGTGGA GGGAGGAATG 1800
CAGGTTGATG GGCTATTTGT AAGCCCATTG TAAAGTAAGC CTTTGTAAAG AGTAAAACAA 1860
TGACTTTGAA AGAGGAAGCT TTTTATTAAA GTTTTAAAGG AAATAGTGTT TTCTTTGCAT 1920
CATGGGCAAA TTCTTCACTG ACCAGACATG AGAAGAATGT ACTCAGATGT GATGTAGGAC 1980
TCTTTTTGGA TATTAAAGAG AAAAATGAAT GAAATCTTTT TACTTTCCCT TCTCTAATTA 2040
ATAAGTGGTT TTATTTCCAT TTGCAGAGGA GGGTGCTTAA ACCATTTTTC TTTCATCAGT 2100
AGTTAGGATT CTGGACCCAG AGCAACCATG GGGTGTGGAG AGAGTGGGAG GGGGTAGAGG 2160
GAGGAAAGGA GTAAACTGGG TTTTTTCAGG GATGAGGAAA GTGGCAGACA GGGTGTGGGC 2220
AGGAGATCTG TACTCCCTTC TTGCCAGGGT ATGTAGATGT TTTACTTTCT TTCACTATCT 2280
GTTGAAGAAC TCTGGTTCTA AGAAATATAT ATGGAGAGCT TTGTATGCTA TAAAGGGATA 2340
TACAGGTCGG GCATGGTGGC TCGCACTCGT AATCCCAACA CTTTGGGAGG CTGAGATGGG 2400
AGGATCGCTT GAACCCAGGA GTTCTAGACC AGCCTGGGCA ACATAATGAG ACCCCCATCT 2460
CTACAGAAAT GTTAAAAAAT TAGCTGGGCA TGGTGATATG CACCTGTACC CTTAACTACT 2520
TGGGAAGCTG AGGTGGAAGG ATCACTCTGA GTTCATCTTA GAGGTACAGA ACCCAAATAA 2580
CACAGCAAAG AGCCCCAGAG TCTGGAGTGA GAAGAGTGCT GCTCTCTGGT GCTAGAGACC 2640
ATGTGAAGAA GGGAAGAATA CCCACATCTG ACTAAGCATA TGTGTAAATG CACCTTCCTC 2700
TCTGAGACAA AGAGCTGTAG TATGGGGCTT 2730
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