| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01598 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:207141580-207143430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFG | MA0659.1 | chr1:207142524-207142545 | TAAGTGCTGATGCAGCACATG | + | 6.1 | | PROP1 | MA0715.1 | chr1:207142443-207142454 | TAATTTGATTA | - | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23166 | chr1:207141832-207143705 | Colon_Crypt_1 | | SE_24017 | chr1:207141819-207142508 | Colon_Crypt_2 | | SE_24017 | chr1:207142691-207143558 | Colon_Crypt_2 | | SE_26377 | chr1:207140549-207143554 | Duodenum_Smooth_Muscle | | SE_28474 | chr1:207140000-207149527 | Fetal_Intestine | | SE_29373 | chr1:207139921-207149527 | Fetal_Intestine_Large | | SE_58988 | chr1:207121014-207154864 | Ly3 |
|
Enhancer Sequence | GACTGAGGCA GTAGAATTGC TTGAACCCAG AAGGCAGAGG TTGCAGTGAG CCCGTGCCAC 60
TGCACTACCA CTTGGGTGAC AGAGCAAGAC TCTGTCTCAA CAACAACAAC AACAAAAAAG 120
ACAGAGATTG TACATTACAC TTCTCTTGTA TTCCCCAGAG GGTATTCATG GATGCTTTTT 180
GATGGATTAA AAATCTACTC TTTGAATCTA TCTATTGCTT CTGTTTCTGA GACCTATAGA 240
TTTTTGAAAA AGCAAACTAA AGTTAGCCGT TGAGTTTTTC TTCCTACTCT AATACGTTCC 300
TCACTACTGT TAAGGACAGG CGCTAACAGT CAATGGTTTG GCCCATGGGC AGAAACCCCC 360
TCACTCCCCA AACAGTTTAA GCCATGCAAA ACCACTGGCC AGTTTGTGAC ACAGGCTGTG 420
CAGGAGGGAA TCACAAAGAG GAAAACAGGG AATAGGGGAA AAGAGAAGGC AGAGGAAGTA 480
GGAGAACAGG GAGAGAAAAG GAGAGGTAGG AGGTGAAAGA AGGGAAAAGG GAAGAGAGAA 540
GACAGAAGCA GAGAAAAGTA GAGAGTCCAT GGGGTGGCCC TGAGCTTGTT TTCCTGCAAC 600
TAGACTTGGC AAGTTGTCCC CTCAGCTTGG CTCTGCCCAG CCCTCTCCAC TAAGGCCTTT 660
CCCTGCTCTA CCCAGTTTGA GCCCCAAGAA TGGCCAGATC TTTAAAAGTC CATAGGCTCT 720
TTATGCATCT TTCTGTGCCT TCGCTGTAGC AAGTCCCCTA GCTTGGGCAC TGCGATGGCA 780
GTCTCAGACC TTTCCCTGCC TTACAAAGCT TCCTGTCCCC ACCTGGAGAC TCTCCCAGGG 840
TGTTTGTTCC TGCACCTAAC TCATAATTTG ATTAATATTC ACCAAGTCCT GGCTGATTCT 900
GGGGCTGGTA CCTAGACTCC CCCGGGTGAA TTTTTCTAAA GCACTAAGTG CTGATGCAGC 960
ACATGTTGGG GCCAAAGTCT CTGCATCATA CCATCCAGTT CCTCTGAAGT CACCGGTGCA 1020
GCAATCTCTG GGCTTCAGGG AGAAAAGCCG GCTCCGTGGG GCAATGAGGA AGCAGGAGTA 1080
TGAGATAAAA TGTTTCCAGG GAGTTATCAG CTTTGATTGG AGGCTGGGAG GATAATACTC 1140
AACGGAATGT CTCCAAGTCA CCCTCTCTGC CAATGACCTT CAGAAATCCT TTCTCCAGGA 1200
GACAGGGGGC CATAATTCAG TAGCCTGGGG CCACAGGCTT CTGTTACTGC ACACTGCGTT 1260
TTAGGGGATG AGACCATATG AGGGGACTCT CTTGTCCCTC TCATCCTGCT GGGAAGGGCA 1320
TGCACCTCAC CTCAGCTTCA GCACAGGCTG CTTGCTGCAT GACTTCCCAG ATGCCTACTG 1380
GCCCTCCGAG CCCCAGTTCA CTCCTATCCC CTCCCCACAT CCCCTGGGCA GCAGATAAGA 1440
AGGGAAGGAG TCAGTGTAGT ATAGAGGAGA GAGCACAGAA CCAGGACTCA GGAGGGGCTG 1500
CAGCAGCCTC AGGCTGCTGC AATAACTTGG CCAATGTTCT GTTCCTCTCC TCTACAAAAG 1560
AAGAGCTTTG ACTGCATGTT CTCCGTGTTT CTTCTCTTTC TAACGTTTTT TTGGTTCTAA 1620
ATTACCCAGG ACTTCTAAGG AACCATGCAC TCTGGTGGGT GTGAGCAGAA TAATAGGGAG 1680
CTGAGAGGGA GCCCCTATGT TCTGGACTCT AGAACCCTTA CCTGGCCTCC TGGGAAGGAG 1740
CCCACCTGCT CTGGGAAGGG CACTGAGGAG CATGTGTGAC AGCTATGGCT GCAGTTCACC 1800
CCCCACATTC AGAGGCAAGA TCCCAACCTC CAGGAGAAAG CATCATTTCA 1850
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