| Tag | Content |
|---|
EnhancerAtlas ID | HS118-00486 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:44036460-44039360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLIS1 | MA0735.1 | chr1:44038702-44038718 | TGACCCCCCAAGTAGG | + | 6.19 | | GLIS3 | MA0737.1 | chr1:44038703-44038717 | GACCCCCCAAGTAG | + | 6.06 | | LMX1B | MA0703.2 | chr1:44036477-44036488 | TTAATTAAAAC | - | 6.14 | | LMX1B | MA0703.2 | chr1:44036517-44036528 | TTAATTAAAAC | - | 6.14 | | LMX1B | MA0703.2 | chr1:44036474-44036485 | AATTTAATTAA | + | 6.32 | | PHOX2A | MA0713.1 | chr1:44036473-44036484 | TAATTTAATTA | + | 6.62 | | PROP1 | MA0715.1 | chr1:44036473-44036484 | TAATTTAATTA | - | 6.32 | | PROP1 | MA0715.1 | chr1:44036473-44036484 | TAATTTAATTA | + | 6.62 | | Phox2b | MA0681.1 | chr1:44036473-44036484 | TAATTTAATTA | + | 6.62 | | Znf423 | MA0116.1 | chr1:44038128-44038143 | GGCACCTAAGGGGCC | + | 6.41 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_00616 | chr1:44036802-44039405 | Adipose_Nuclei | | SE_03403 | chr1:44038611-44039097 | Brain_Angular_Gyrus | | SE_04240 | chr1:44038071-44039804 | Brain_Anterior_Caudate | | SE_05040 | chr1:44033899-44037467 | Brain_Cingulate_Gyrus | | SE_05040 | chr1:44037598-44040003 | Brain_Cingulate_Gyrus | | SE_05962 | chr1:44033964-44040045 | Brain_Hippocampus_Middle | | SE_07193 | chr1:44038175-44039985 | Brain_Hippocampus_Middle_150 | | SE_08033 | chr1:44036769-44039793 | Brain_Inferior_Temporal_Lobe | | SE_27645 | chr1:44037146-44038216 | Fetal_Intestine | | SE_28595 | chr1:44037272-44038173 | Fetal_Intestine_Large | | SE_33537 | chr1:44038191-44039825 | H2171 | | SE_41575 | chr1:44036638-44039606 | LNCaP | | SE_52524 | chr1:44037150-44038079 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 44037830 | 44038114 | | chr1 | 44038690 | 44038861 | | chr1 | 44039223 | 44039320 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043570 | chr1 | 44036639 | 44041999 |
|
Enhancer Sequence | GTGTTAGCTC ATTTAATTTA ATTAAAACTC AACAAGATGG AGGCAGCTGT AGCGCAGTTA 60
ATTAAAACAG CCATAATCAA GGCAGCAAAC GGCCGGCAGT GTTTGTGGCC GCTGCCCAGC 120
GCAGCACAGC GGCCAGCACG GTTCGGCTCC TCTGCATTTT CTCATAGTTC CTCCAGGCAG 180
GCTCCCCAAG CAGCCAGACG CTCCTCCCTG CTGGCCTGGG CCCCTCCACA GAACCACATG 240
GACTTGTCTG GCAGCAGCTC TGGGAAGGCT CGCTCACACA TTGGTTCATC TAGTATTTAT 300
ATAGTGCTTG GGGTGCCCGG CCCTGGGCCA CCCCTTCCTT GCCTATCACT CCACTGGATG 360
CCACTCAGGC CCCATCCTCC TTGTCCTCTC GGCAGCAGCT AACATTCCTC CCTCCTTCCC 420
AACCACACTC CCATTTTTCC CTAGCCTTTC AGGGCTCTGT CTCTTGCGAC TTCCCTCTTC 480
CTAGTGCCCC TTCCCTGCAG CAGCATCTTC CCTTCCACCA AGCCCTGCCT TTGCCCTATG 540
GACACAGCCT TGCCCTGGAC GAGCTCACCC CCTCCTAAAG CTCCAACTGC CATCTCCTCA 600
CCTGCAACTC TAGCTTTAGT CTTTCCAGCC CAAACCTCTT ACCTGAGCTC TAGATCCAAA 660
ATTCGACCTG CCTTCTGGTC ACCCTGACCA GTGGTGATCA GTGATGAGTG ATGACCTTCT 720
TTTCAGACAG CTGTACCCTC TTTCCATAAG TGGCACCCTC CAACCTGGAA CATGGGTCTC 780
AAGTTGGTTT GAGAGCTCTC AAATGTACCA CCCTCGTGGC TCTCAAATTG GCCCCCTTCT 840
CCCCTCCTGC TGCGTCAGTC CTATCCCAGG CACCAGACAC TGCTTTCCCT GCCTCCGGGC 900
CCTCCCGAGA ATCCATCATC CTGTAGGTCA GGTTTGCTGC TCATACCTTC CTGTGCCTCA 960
GTGGTGTCTC CTTGCCTACC TGGTCAAGTG ACGCTCCCAA GCAAGGCTTA GAGGGCCCTT 1020
CTTGGTCTTC CCCTGCCCGT GTCTCATCGG GTCCTGGCTA CACCACTTAC CAGCTCTCTG 1080
GCATTGGTTA ACTTTTTCGT GTGTCAGTTT TCTCATGTTT GAAAAGGAGT TACAGTAAGC 1140
AGTGAGTGAG TCAATGGCAG TCAAACCTTG AGTTGATGGC CTGGCCTCTG GTAAGGGCTT 1200
CATGGAGCTC TTTCTACTTT CTGTGCCCTT GACCCTCCTA ACACTGAGCT GTGCTGACCC 1260
GTCCTTGGTC CTTGCCCACC TCCGGCCCTC TGCTCACCTT CCGGCTGCTC CACTTGAAAA 1320
CCTCCACCCT GCTCAGCCTC TGGCTGCTGC CTCAGGCCTC ACCTTGCTTT ACATTGTCAC 1380
CATCTGGCTC CAGTTCTGCT CAGCTAGGCC TTGCAGGGAG GGCCTGGGTC TGATCACACT 1440
TGGTGAGGTC AGCTGTAGGA CAGGTCTTCT CTGAGCCCTT GTCAAGTGAA TGATTTCATG 1500
AACTTGACCT TTGGCACTTG TCCCTGTAGG CTAATATCTG CTCTAATGTT CACTCCTCCT 1560
TCTGCTTTCC AGGTCCAAGG AAGACTTCCT TATTTGTCTT CCTGCCACCT GGAAGTTGTG 1620
ACCTCAGGGT CGTGGGCCCA GGGTCCAGCT CCTGGGATGG AGCCAGATGG CACCTAAGGG 1680
GCCTCAACCA TCCCACCTCT GCAGTAATAA CTGGGCTCTC TCCCCTCCCT GCCTGACCTG 1740
GCCTGGGACC GTTGGCCTCA GTTGTTGCTG GCCTTATCCC ATTACCATTT AGAAGGGTGC 1800
TAAGGCTATT CCGTGCACAT TTTTCAGGGA CAGCCCTTCA TGGAGTGGAC TCAGGCCCCT 1860
GAGCACTCAG CTGTTTACCG GGACCTTTAC GGTTTACGCA TCACCGACAG TTTACAACAG 1920
AGCTTTCCCC GCTTTTGTTG CAGCTGATTC TCTTGCAGCC CTGTGAAGTA GGACAGGCTG 1980
TGATTACCAT GCCCCCTTCA CAGCTGAGTT AAGGGAGTCA CTTGGGGTCA CACATCGAGA 2040
CTCGGCCTAG GAGCTCCCCT GTGAGATCAC CTCAGGACCT AGTATCACAA TAGCAAACCT 2100
GGGGACCTGA GGAGCAGCTG GACCCTTCTG GGGCTTCAGA GCTGCACATT CCCAGCTTCT 2160
CCAGACCCCA GGCCCCCACT GACCAGTACC CAGAAGTCCT CCACCATCTG CAACCTGAGC 2220
CACAGCACAT CTAACCAGGG CATGACCCCC CAAGTAGGAG CTGGACAGGA GGTAGCTGAC 2280
GGCATGCGCT GCCCAGATGT GAGCTCTGCT CAGCAGGCCT TTTCTTCTCT GTAGTGATGT 2340
GACATGCTGC CAAAACCACC TCCTGGAGAA TTGGAACTTG AGACCGGGGT AGGCCCAGGA 2400
GGAACAGGAA CAAGCTTATA GAGTGGAAAT GGAGTTGTGA GCAGGGGCTC AGAGCCCCTG 2460
CTGGGTCCTG AGAGGAGCTG TTGGCCTGCA GGCTGTGCCG AGCCTGGACA GGGCTTGAGG 2520
AGATTCCCGC ACTCCTGCTG TGGCCTGAAC ATATGAGCTG CCATCCTTTG TCGTAGAGGA 2580
CAGCCTAACT CACTAAGTCC ATGTGCTCAT CCAGAGAGCA GTCTCTTCCC CACCCCCAGC 2640
ACCCTGAGGC GAAACCTGGG GGTCTTAAGA AGAGATGCAG CATCTGGCTG CAGGAGGAGG 2700
CCCGTGGGTG GGACGCAGAG GGCTTGCAGC CCCTCACCCT GCTGGCTGGC CCCAGCTCTG 2760
GCTGGAAGAG CCTGTCCCCA CCCCACTCTG CTCTGCCATC TGCGGGGCCT GCCAGGAAGG 2820
CACACTGCCA GTGCATGCTC ACAATTTCCC TTTGGCCCAG AGCTCCCTGG CACCTCTTGG 2880
ACACGAATAC ACCCCTAAGG 2900
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