Tag | Content |
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EnhancerAtlas ID | HS047-35004 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr9:130878630-130879980 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr9:130878641-130878651 | ACCACTTGAG | + | 6.02 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_23076 | chr9:130874973-130879280 | Colon_Crypt_1 | SE_23771 | chr9:130878517-130879308 | Colon_Crypt_2 | SE_24841 | chr9:130878562-130879306 | Colon_Crypt_3 | SE_25948 | chr9:130875257-130879294 | Duodenum_Smooth_Muscle | SE_27710 | chr9:130875276-130879436 | Fetal_Intestine | SE_28658 | chr9:130875225-130880296 | Fetal_Intestine_Large | SE_31462 | chr9:130874952-130880613 | Gastric | SE_53121 | chr9:130874806-130879385 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I128112 | chr9 | 130875084 | 130880679 |
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Enhancer Sequence | GAGGTGGGTG GACCACTTGA GCCTAGGAGT TCAAGGCTGC AGTGAGCCAT GATCGTGCCC 60 CTATACTCTA GCCTGGACAA CAGAGCAAGA CCCTGTCTCA AAAAAAAAAA AAAATGAACA 120 GACACACAAA AGCAAACCCG CACCCTCCCC ATGAGCTCAC TCTCCTCAGG GAGGACGGAG 180 CTTGCTGTTC TCAGGACTCT TTCCATTCTT ACTTCCTGGA GTCCTTGACC TGGAGCTCTT 240 TAAGCCAGTG GGGAACACAG CAGGGCATGT GTTCTGAGAA CAGACAGCAG ACCCTACCAG 300 CTTCATAAAT AGACCCCTCG AATATTGACT CTGTGTATCG TCATCCAAAA CACCTTCCCA 360 GCCCTGGCCT TACCCGCCCA CGGAGGTTTA CTAATGCCAT TTCCCAGTCA GTAAGGGGCT 420 TGCCCAAGGG CACAGTGGGC AGCGGCCGGG TCCTGAACTC AGGCCTTCTG AAGCCATCAA 480 GACCACAGGG GACCGTGAAT GGTGGCTCAC ACCTGCAATC CTAGCACTTT GGGAGGCCAC 540 GGCGGAAGGA TTGCTTGAGG CCAGGAATTT CAGACCAACC TGGCCAACAT AGCAAGAACC 600 TGTCTCTATG TTTTATTATT TATTTGTTTA GAGATGAAGT CTCCCTCTGT CGCCCAGGCT 660 GGAATACAGT GGCACAGTCT TGGCTCACTG CAGCCTCCAT CTCCCAGATT CAAGCGATTC 720 TCCTGCCTCA TCCTCCTGAG TAGCTGGGAT TACAGGCATC CACCACCAGA CCCGGCTAAT 780 TTTTGTATTT TTAGTAGAAA CAGGGTTTCG CCATGTTGGC AGGCTGCTCT CTCAAACTCC 840 TGACCTCAAG TGATCCACCC GCCTCACCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC 900 ACTGCTCCTG GCCTCTTTTT TTTTTTTTTT TTGAGACGGA GTCTTGCTCT GTTGCCCAGG 960 CTGGAGGGCA AGTGGCGCAA TCTCGGCTCG CTGCAACCTC CCCGGCCTCT ATTTTTTAAA 1020 CAAAGAAAGA AAAAATGACC ACAGGGGCCA TGCCGTGACC TGAGGATGGC ACTAATGGGC 1080 CATGGAATCC TGGCTTGGGG CCCGTTCCTA AGAAGAGACA TTTCTTCTTC TTTTTTTTTT 1140 TTTTTTGAGA GGGTCTCACT TTGTCACTCA GGCTGGGGTG CAGTGGGACA ATCATAACCT 1200 CACTGCAGCC TCAAACTCCT GGGCTCAGGT GACCCTCCCA CCTCAGCCTC CTGAAGTGCC 1260 GGGCTTACAG GGATGAGCCA CTGTGCCCAA CCTCAAGAGA CATGTTTTTT CCTAGCCACT 1320 CATCTTTGGA CCCTTACAGC TAAGCCCATT 1350
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