| Tag | Content |
|---|
EnhancerAtlas ID | HS091-01259 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:36668510-36671400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr1:36669828-36669843 | AGGGCAGGCTGACCT | - | 7.55 | | NKX2-5 | MA0063.2 | chr1:36668699-36668709 | CTCAAGTGGT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:36671235-36671250 | GAGGTCAGGAGTTCA | + | 6.22 | | RREB1 | MA0073.1 | chr1:36669953-36669973 | ATGGTGGGGGTGGGTGGGTG | - | 6.09 | | RREB1 | MA0073.1 | chr1:36669965-36669985 | GGTGGGTGGGTGGGGGGTGT | - | 6.55 | | RREB1 | MA0073.1 | chr1:36669957-36669977 | TGGGGGTGGGTGGGTGGGTG | - | 7.58 | | RREB1 | MA0073.1 | chr1:36669961-36669981 | GGTGGGTGGGTGGGTGGGGG | - | 8.79 | | Tcf12 | MA0521.1 | chr1:36669281-36669292 | AACAGCTGCTG | + | 6.32 |
|
| | Number of super-enhancer constituents: 18 | ID | Coordinate | Tissue/cell |
| SE_03303 | chr1:36668859-36669950 | Brain_Angular_Gyrus | | SE_04066 | chr1:36668642-36670588 | Brain_Anterior_Caudate | | SE_05024 | chr1:36668499-36670996 | Brain_Cingulate_Gyrus | | SE_05887 | chr1:36668484-36671079 | Brain_Hippocampus_Middle | | SE_06862 | chr1:36668431-36670706 | Brain_Hippocampus_Middle_150 | | SE_07920 | chr1:36668568-36670940 | Brain_Inferior_Temporal_Lobe | | SE_26652 | chr1:36668722-36670470 | Esophagus | | SE_31707 | chr1:36668687-36670477 | Gastric | | SE_37181 | chr1:36668315-36671203 | HSMMtube | | SE_42156 | chr1:36668410-36670672 | Lung | | SE_42156 | chr1:36670696-36671441 | Lung | | SE_48111 | chr1:36668314-36670674 | Psoas_Muscle | | SE_48599 | chr1:36668452-36670657 | Right_Atrium | | SE_48599 | chr1:36670712-36671339 | Right_Atrium | | SE_49470 | chr1:36668484-36670597 | Right_Ventricle | | SE_49470 | chr1:36670844-36671269 | Right_Ventricle | | SE_54589 | chr1:36668333-36671420 | Stomach_Smooth_Muscle | | SE_65351 | chr1:36668762-36670397 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I036202 | chr1 | 36668509 | 36670600 | | GH01I036205 | chr1 | 36670697 | 36671441 |
|
Enhancer Sequence | CTAGGCTACA GTGCAGTCGC GCGATCTTGG CTCACTGCAA CCTGCTCCTC CCGGCTTCAA 60
GCGATTCTCC TTGAATCGCT TCCCAAGTAG CTGGGATTAC AGGCGCCTGC CACCATGTCT 120
GCTAATTTTT GTATTTTTAG TAGAGACTAA AACCAACATG ATTGGTCAGG CTGATATTGA 180
ATTCCTGACC TCAAGTGGTC TGCCCGCCTC AGCCTCCCAA AAGGAATGGA ATCTTAAAAA 240
AAAAAAAAAC AGTGATGGGA ACAGGATCTC ACTATGTTGC CCAGGCTGGT CTTGAACTCC 300
TCCTGACTGA ACCTCCCAAA CTGCTGGGAT TACAGGTATG AGCCACCATG CCTGGCCAAA 360
AGTCCCTCAA CTTTCTGTTT TAAAAATTGC CACCAGACTT TTCTGCAATG TCACCTGAAG 420
GGTTCCTGGT CTCACACAAT GCCCACCCCT AAAACACAGC AGCCTAGGCC ACCACGTTCT 480
GCCAGGCGAG GTGTGTGGTA GGAAGAGGGC AGGCAGCTCT GGCCTCAGGC ACAAAGGGCT 540
GAGTCCTGGG TCCTGGGGAC AGGCACTGGC AATTGAATCT GGACACTGAG CACTGGGTCC 600
TAACACAAGA AATCATTTCC TGGCTCAGGG CAGTGATCTC TGGGTCCTAA AAACTAGGAC 660
CAGAGCAGAG ACCATAGGTC CCTTATCTCT GGGCGGAGGG TGCTGGGCTA AGTGGCAGTC 720
ACCCAAGGCA GGGCCAGGGG TAAGGAGATG CCCAGCCCCC AGTTGTTTTG TAACAGCTGC 780
TGGACTGGGC TGGAGGGGAA ATTTAAGGAA CCAGGGGGTG AGGTAAGGAG GAAGAGGTCA 840
GTGGGCAGGG CAAGGCCACT CGGGCATGCT GGATTGGTCC CAGGCCCTGG AGGGCGAGAG 900
AAAGACAGTG GCTGGATCTC TAGGGCTCTC ATTGGCAGAC ACTGGGGCCC CAGGAACTAG 960
GGCAAGAAGA GTGGTGAGGA TAGCAGGGAG TGTGTGCTAC CCCCTACCCC CAACCCCCCT 1020
CTTTGTACCC TCCCCCCTTT GTCAACCTCC TGGCTCCGCT CCCAGGCCGA GGCAGCTGGA 1080
GTGATTAGTG TGGGTGAAGG AGTACAAATG CCAAAGGCTT GTCTCACGTC TCAGAACACA 1140
GGGATCCAGC CAGAGTGGAT GGCACAACTG AGTGAGAAAT GGAGACCGAG AGATAAACAG 1200
AAATAAACAG GGACAACACC AAAGAGATAG AGGAGAGAAG CAGGGCGGGA GACAAAAGAA 1260
GAGACCAAAG GCCCACACAG AGCAAGGGGG TTGTGGGGAG GGAGGGTTCA GTAGCTACAG 1320
GGCAGGCTGA CCTTTTCCTG TCTCTTCTCT GACCCCGTCC TGTCTGAGTT CCCCTCCGCT 1380
GTGTCCCTAT CCCAGGCTTT CTCAACCTCA GCACTGTTGA CATTTGGGGC AGGATAATCT 1440
TGGATGGTGG GGGTGGGTGG GTGGGTGGGG GGTGTTCTGT GCCCTGTAGG ATGTTTAGCA 1500
GCCTCCTTGG CCCTTATCCA CCACATGCCA TTGGCACTCC CCCAACTCCT CTGCTCTTGT 1560
GACAATCCAA ACTGCCTCCA GATATTGCCG GATGTTTCCT GGGAAGGGAT TGCTCCTGAC 1620
TGAGAACTGT CCCCAGGTAG GTTCATGTTC TTGAGAAGAG GCTACCCCAG GGTGTCTGGC 1680
TGGTTCTCCC TTCGGCCCGT GTGCACAGGG CCCCCTGGCT CTAGCATGGC TTAAGTTGCC 1740
CTAAGTCAGA AGCCGGGGAA ACTAGGAGAG CCACTGAGAC TGAAGAGCAG TCTAGGTACA 1800
GCAGTAACGA AGTCCCTGCC CTCATGGAGC TTCTGTTCTT ATTCCACCCA AAAGGCATCC 1860
CAGGTGTGTT TTGGGATGTG CTAGGGGTGT TTCATGAGTG GGTGTGCACT CTCGTCTCTA 1920
AGGGAGGAAG AAGAGATGGG CCCCCAAGTA TGTCTGGACA AGATACAGGT AACAAATATG 1980
CATTTTATTC CATGATGCTT AGATGTAAGA AATGTCCCAT TTATCCAGGC ATGGTGGCTC 2040
ACACCTGTAA TCCCAGCACT TTGGGAGGCT GAAGCGGGCG GATCACGAGG TCAGGAGATT 2100
GAGACCATCC TGGCCAACAT GGTGAAACTC CGTCTCTACT AAAAATACCA AGAAATTAGC 2160
CAGGCGTGGT GGCGGGCACC TGTAGTCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATGG 2220
CATGAACCCG GGAGGCGGTG CTTGCAGTGA GCCGAGATCG CGCCACTGCA CTCCAGCCTG 2280
GGCAACAGAG CAAGACTCTG TCTCAAAAAA AAAAAAAAGA ATTGTCCCAT ATATTTAATT 2340
CTCTAAACCA GATGATCTGC TCCAAAAACC CCCTGCCAGG CTGGCTGGTG AGAAATTCAA 2400
TCACAGTCAT GTTTTGGGAA TCTCTACCCA GTGGTGTGCT GGTGAATGTT TACAAATGGT 2460
TTGGGGTGCA TTAGGGAGGG ACTTGATTTG TCACATTTGC CAACTTCCAT GATGTAAACA 2520
CTCCCACCAT GGCCAATTTC AAGCTGCCAA CATAATGTCA GTGCAGGTGG AGCAGGGAGG 2580
AGTGAGCAAT GGCACACTGT CACACAGGGT ATTCACCCGG CAGATGCCAA CAACTTTAAA 2640
AGGATTGATA ATAGTAAACT GGGCCAGGTG TGGTGGCTCA TGCCTGTAAT CCCAGCACTG 2700
GGAGGCTGAG GTGGGTAGAT CATCTGAGGT CAGGAGTTCA AGACCAGCCT GGCCAACATG 2760
GCAAAACCCT GTCTCTACTA AGAATACAAA AATTAGCTGG GTGTGGTGGC ACAAGCCTGT 2820
AATTTCAGCT ACTCAGGAGG CTGAGGCTGA AGAATTGCTT GAACCTGGGA GATGGAGGTT 2880
GCAGTGAGCC 2890
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