| Tag | Content |
|---|
EnhancerAtlas ID | HS179-00667 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:36668650-36671380 |
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 | TAGAGACTAA AACCAACATG ATTGGTCAGG CTGATATTGA ATTCCTGACC TCAAGTGGTC 60
TGCCCGCCTC AGCCTCCCAA AAGGAATGGA ATCTTAAAAA AAAAAAAAAC AGTGATGGGA 120
ACAGGATCTC ACTATGTTGC CCAGGCTGGT CTTGAACTCC TCCTGACTGA ACCTCCCAAA 180
CTGCTGGGAT TACAGGTATG AGCCACCATG CCTGGCCAAA AGTCCCTCAA CTTTCTGTTT 240
TAAAAATTGC CACCAGACTT TTCTGCAATG TCACCTGAAG GGTTCCTGGT CTCACACAAT 300
GCCCACCCCT AAAACACAGC AGCCTAGGCC ACCACGTTCT GCCAGGCGAG GTGTGTGGTA 360
GGAAGAGGGC AGGCAGCTCT GGCCTCAGGC ACAAAGGGCT GAGTCCTGGG TCCTGGGGAC 420
AGGCACTGGC AATTGAATCT GGACACTGAG CACTGGGTCC TAACACAAGA AATCATTTCC 480
TGGCTCAGGG CAGTGATCTC TGGGTCCTAA AAACTAGGAC CAGAGCAGAG ACCATAGGTC 540
CCTTATCTCT GGGCGGAGGG TGCTGGGCTA AGTGGCAGTC ACCCAAGGCA GGGCCAGGGG 600
TAAGGAGATG CCCAGCCCCC AGTTGTTTTG TAACAGCTGC TGGACTGGGC TGGAGGGGAA 660
ATTTAAGGAA CCAGGGGGTG AGGTAAGGAG GAAGAGGTCA GTGGGCAGGG CAAGGCCACT 720
CGGGCATGCT GGATTGGTCC CAGGCCCTGG AGGGCGAGAG AAAGACAGTG GCTGGATCTC 780
TAGGGCTCTC ATTGGCAGAC ACTGGGGCCC CAGGAACTAG GGCAAGAAGA GTGGTGAGGA 840
TAGCAGGGAG TGTGTGCTAC CCCCTACCCC CAACCCCCCT CTTTGTACCC TCCCCCCTTT 900
GTCAACCTCC TGGCTCCGCT CCCAGGCCGA GGCAGCTGGA GTGATTAGTG TGGGTGAAGG 960
AGTACAAATG CCAAAGGCTT GTCTCACGTC TCAGAACACA GGGATCCAGC CAGAGTGGAT 1020
GGCACAACTG AGTGAGAAAT GGAGACCGAG AGATAAACAG AAATAAACAG GGACAACACC 1080
AAAGAGATAG AGGAGAGAAG CAGGGCGGGA GACAAAAGAA GAGACCAAAG GCCCACACAG 1140
AGCAAGGGGG TTGTGGGGAG GGAGGGTTCA GTAGCTACAG GGCAGGCTGA CCTTTTCCTG 1200
TCTCTTCTCT GACCCCGTCC TGTCTGAGTT CCCCTCCGCT GTGTCCCTAT CCCAGGCTTT 1260
CTCAACCTCA GCACTGTTGA CATTTGGGGC AGGATAATCT TGGATGGTGG GGGTGGGTGG 1320
GTGGGTGGGG GGTGTTCTGT GCCCTGTAGG ATGTTTAGCA GCCTCCTTGG CCCTTATCCA 1380
CCACATGCCA TTGGCACTCC CCCAACTCCT CTGCTCTTGT GACAATCCAA ACTGCCTCCA 1440
GATATTGCCG GATGTTTCCT GGGAAGGGAT TGCTCCTGAC TGAGAACTGT CCCCAGGTAG 1500
GTTCATGTTC TTGAGAAGAG GCTACCCCAG GGTGTCTGGC TGGTTCTCCC TTCGGCCCGT 1560
GTGCACAGGG CCCCCTGGCT CTAGCATGGC TTAAGTTGCC CTAAGTCAGA AGCCGGGGAA 1620
ACTAGGAGAG CCACTGAGAC TGAAGAGCAG TCTAGGTACA GCAGTAACGA AGTCCCTGCC 1680
CTCATGGAGC TTCTGTTCTT ATTCCACCCA AAAGGCATCC CAGGTGTGTT TTGGGATGTG 1740
CTAGGGGTGT TTCATGAGTG GGTGTGCACT CTCGTCTCTA AGGGAGGAAG AAGAGATGGG 1800
CCCCCAAGTA TGTCTGGACA AGATACAGGT AACAAATATG CATTTTATTC CATGATGCTT 1860
AGATGTAAGA AATGTCCCAT TTATCCAGGC ATGGTGGCTC ACACCTGTAA TCCCAGCACT 1920
TTGGGAGGCT GAAGCGGGCG GATCACGAGG TCAGGAGATT GAGACCATCC TGGCCAACAT 1980
GGTGAAACTC CGTCTCTACT AAAAATACCA AGAAATTAGC CAGGCGTGGT GGCGGGCACC 2040
TGTAGTCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATGG CATGAACCCG GGAGGCGGTG 2100
CTTGCAGTGA GCCGAGATCG CGCCACTGCA CTCCAGCCTG GGCAACAGAG CAAGACTCTG 2160
TCTCAAAAAA AAAAAAAAGA ATTGTCCCAT ATATTTAATT CTCTAAACCA GATGATCTGC 2220
TCCAAAAACC CCCTGCCAGG CTGGCTGGTG AGAAATTCAA TCACAGTCAT GTTTTGGGAA 2280
TCTCTACCCA GTGGTGTGCT GGTGAATGTT TACAAATGGT TTGGGGTGCA TTAGGGAGGG 2340
ACTTGATTTG TCACATTTGC CAACTTCCAT GATGTAAACA CTCCCACCAT GGCCAATTTC 2400
AAGCTGCCAA CATAATGTCA GTGCAGGTGG AGCAGGGAGG AGTGAGCAAT GGCACACTGT 2460
CACACAGGGT ATTCACCCGG CAGATGCCAA CAACTTTAAA AGGATTGATA ATAGTAAACT 2520
GGGCCAGGTG TGGTGGCTCA TGCCTGTAAT CCCAGCACTG GGAGGCTGAG GTGGGTAGAT 2580
CATCTGAGGT CAGGAGTTCA AGACCAGCCT GGCCAACATG GCAAAACCCT GTCTCTACTA 2640
AGAATACAAA AATTAGCTGG GTGTGGTGGC ACAAGCCTGT AATTTCAGCT ACTCAGGAGG 2700
CTGAGGCTGA AGAATTGCTT GAACCTGGGA 2730
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