Tag | Content |
---|
EnhancerAtlas ID | HS043-01398 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:54763700-54766420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:54764892-54764903 | CCACACCCTCT | + | 6.02 | RUNX1 | MA0002.2 | chr1:54764137-54764148 | AAACCACAGAG | - | 6.14 | TCF3 | MA0522.2 | chr1:54764328-54764338 | AACACCTGCT | + | 6.02 |
|
| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_01019 | chr1:54763385-54764722 | Adrenal_Gland | SE_01595 | chr1:54763205-54766233 | Aorta | SE_03451 | chr1:54763335-54764813 | Brain_Angular_Gyrus | SE_03451 | chr1:54764968-54767093 | Brain_Angular_Gyrus | SE_04187 | chr1:54762347-54767014 | Brain_Anterior_Caudate | SE_04901 | chr1:54759648-54768125 | Brain_Cingulate_Gyrus | SE_05919 | chr1:54759767-54771349 | Brain_Hippocampus_Middle | SE_07802 | chr1:54760466-54768146 | Brain_Inferior_Temporal_Lobe | SE_08904 | chr1:54763438-54764392 | Brain_Mid_Frontal_Lobe | SE_08904 | chr1:54765775-54766227 | Brain_Mid_Frontal_Lobe | SE_24580 | chr1:54763280-54765674 | Colon_Crypt_2 | SE_25961 | chr1:54763062-54766000 | Duodenum_Smooth_Muscle | SE_26701 | chr1:54761810-54766205 | Esophagus | SE_28122 | chr1:54763260-54766102 | Fetal_Intestine | SE_29698 | chr1:54763517-54764671 | Fetal_Muscle | SE_29698 | chr1:54764992-54767546 | Fetal_Muscle | SE_31383 | chr1:54763224-54766540 | Gastric | SE_33414 | chr1:54760874-54771052 | H2171 | SE_41585 | chr1:54763231-54765192 | LNCaP | SE_41585 | chr1:54765226-54766268 | LNCaP | SE_42582 | chr1:54763182-54765442 | Lung | SE_46626 | chr1:54763560-54764562 | Ovary | SE_46626 | chr1:54764577-54765151 | Ovary | SE_46626 | chr1:54765333-54765708 | Ovary | SE_47967 | chr1:54763774-54764522 | Pancreas | SE_50141 | chr1:54763195-54766115 | Sigmoid_Colon | SE_52383 | chr1:54763209-54766161 | Small_Intestine | SE_54182 | chr1:54763572-54764609 | Spleen | SE_54942 | chr1:54761882-54766050 | Stomach_Smooth_Muscle | SE_63284 | chr1:54754699-54809827 | NCI-H82 | SE_65414 | chr1:54763199-54766030 | Pancreatic_islets | SE_66951 | chr1:54760874-54771052 | H2171 | SE_68686 | chr1:54763342-54765795 | H9 |
|
| 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 |
GH01I054297 | chr1 | 54762821 | 54766370 |
|
Enhancer Sequence | CTTCTGCCCC CTCATGCTCC CCAACCAGTC TCCTAGGAGG CCTGCAGGAA GCCTCCGGGT 60 GCAGGTCAGG GCTTCAACAG CTGCCCAAAC AGGTATGGGC CCAGATTTAA TTGGCCTCTT 120 GGTTAAGCTT TCTAATCTCA TTAAAGCTGC CTCCATCAAG CAGACCGAGG CTCTGAATTG 180 AATCACAGAA GAGCGCTGCC CTGCCCCACT GTAAGCTGAT TAGGTCTGGG GAGGCCTAGC 240 TCGGACCCCT CTCTGCACTA CCATGCCGTA CGGTCACACG GAAGGCACGA ACCCAGACTC 300 ACGAAGAGGG GCACACTGAC GAGGGGGCAG CAGGAAGGAA GTTCAGCGAA GCAGTCCCAG 360 CAAGGGTGTG GTACCAGACC TGCCTACTCC CACCACTCTG GGGAGCCAGT GCTGTCCCCA 420 GGATTTTCAG TAAATACAAA CCACAGAGTA ATCTGATTTC CTATCTTATC AGTGTGCAGT 480 GCCAGAGGCC ACCCGGCTCC AGGAGAAAGC TGCCCTTCTA GGCAGAGCGT GGGACTCACA 540 ATTACCTCTC CAACTTCTTT TCGTAGCTTT AGAGCTCTAC TTCATTCAGA TGGAAAGGAG 600 GCAGCAGAGG GGTGTGGTGT GGGGCCCAAA CACCTGCTTT CCATCTCTAG AAGAGAGGAC 660 TTGTCTTGCC ACTCACTCTC TCCCTGACCC CTTCCACCTC CACAAGGAGC TACACTGCGG 720 CTCTTCTCCG ATCCAGCTCC TGGACGTCAG CTTCAAAAAC ACCATGGTCA GCGTGTGCAA 780 ACAGCCCTGA GCAAATACGC GTCGCCCACT TCTCCATCAT CTCGCTTTAT CTAAATATAT 840 CCCAAGGAAA TAACTTGGCA GTGGTGAGAA ATTCTGCAGA GGCTCCAAAG TAACAAAAAC 900 AAAACACACA CACACACACA CACACACACA CACGAGCTCT GTTCAAGGTG CCACGCTGAG 960 CTGAGGATAG GCATGGAGAT ACAAACACTC ACAAGGAACA GCCACCCAGG GTGTGCTGGG 1020 GGTTCAGTCC CACTGAGGGT TCGTGCTTGG TTGTTATTAA TATTTAATAG GGAAGACAAT 1080 ATTTTAGAAG AGACAGGACT CTGTGCAGGT TGCAGGCCAG GCTAGCATAG ATGCCCTGTC 1140 CAAGGGAGAT GTTAAGGGGG CACGCCTAGC CAAGTACACA CACACACCCA TCCCACACCC 1200 TCTGGGACTT GCTGCAAGAC ACTGGTATTT TCCGCTCCAC TTGCCAAGAA TGGAGCCACC 1260 CTGCCCTGCA TGCTTGATCC TCAAACTCCT GGAAACAAAG GCGGCAGTCA CGGGGGCGTG 1320 CTAGCACACC TCAGGCACTG GTCCGATGTT CCCCTACCCT CTGCCATTTT CACTAAAGGG 1380 GAAACTAAGG CCCAAAGCAG AAGACAGACA TGCCCAGAAC CTGGCCAGGG TCCCTCTTAC 1440 TCCACCACGC TGTCGATAAT TTGGATAGAG GTGGCTTTTT TTTTTTTTAA TGCATTACAC 1500 ACATCTAGGC TATTCACAAT CACCCCCAAG CCCACCCTTG TGGGCACAGG GAAACAAATT 1560 ATTAGGAAAA TGAGAGTCAA AGGGGCTATG GGCAATCCCC CAAATCATGC CAGCTCTCAG 1620 CAGGCCGGCC CACTTTCTCA GGTTCCACAC AACCACCCCA GTGTCTGCCT TCTCCATCTG 1680 CCATCTAGAC ACGGACATGA GGCCTGGACC ACTACATCAG GCCCCTCATT AGTTTATTAG 1740 CCTTAATCTA CTTCTTTCTC CAAACAGATC AAACCCAGAT CGCTCACACG GCAGGCTCAC 1800 AACCTGAGGA TTTTCTGCTC CTTGCCACAC ACCAGCTCAG CCGAGGCCTT CAGGACCTGG 1860 CCTGAACCAA CCCTCATTCC CAGCTCCACC GACATAATTC CTCCTTCCCT GAACACTGCA 1920 TGTCTTTTTA AGCTTCTATG CATTTGTACA GACTTCCCAG ACACTGGAAT GCTCCTATCA 1980 CAGTCTTCCT TCTCAGTCAC CAATACCAGA ACTCAATAAT CAGTGACACC ATCCAATCCT 2040 AGCTATTTAA AGACAAGAAA ATGGAAGGCC GAGAGAGGGT AAGGGAGCGC CACAGAAGAT 2100 AAGGTTAGCA GTGCTGGACT CGTGGCTGGC CAGAGTCTTC ATTGACTCCA AAAGCCCTCA 2160 AAGACCCTCT CCAACTCAAC AGCCCTACAG CAAGATCAAA CCCAGGAGAG GGCCACTGAG 2220 GACCAAATAT CCAAGAAAGA GGGCCCTTAG GGAGTTCTAG AGGCAGCACA GGAAGAGCTG 2280 GCCTGGGGTC TCAGGAGGCC AGCAGAAACG AGATGCATGC TTGGGCCTGG AAGCCCAGAG 2340 AGTGGAGAGT ATCATCATGT CAGTTCAGCT CAGGGGCCCA GAGCAGGTGC TCGGGGAGGA 2400 TGTGCAGAAC GACCAAGAAT GGTACCTGGC ACACGGAGAC ACTCGGTCAA CATTTGCTGT 2460 TGCACACATT AATGACACAA ATGGCCAATG ACAAACCAGT GCAACACAGA GTACCGCACA 2520 GGCCTGTACT CAGCTCCAGG ATCCCAAAGA AAGGAAGGAT TATTTCTGCC GGAGGGTGGG 2580 GCTTCACAGA GCGGTGACAT CTGATCAGAC ACCATCTGTT ATTTTTCTCT AATTGTTCCA 2640 CATGTGTGAA ATTTTGATTC TCAAGCTAGA ACATAGACTC TGAGAGGGCC AAGACCATAG 2700 CTGCTTTCTC TGCCTTCACC 2720
|