| Tag | Content |
|---|
EnhancerAtlas ID | HS139-46864 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr6:34190280-34193370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr6:34190862-34190873 | AGCTGTGATTT | - | 6.14 | | KLF16 | MA0741.1 | chr6:34191865-34191876 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr6:34191808-34191818 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr6:34191281-34191291 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr6:34191866-34191876 | GGGGCGGGGC | - | 6.02 | | RREB1 | MA0073.1 | chr6:34192052-34192072 | CCCCCACCCACGCCCTCCCC | + | 6.77 | | SP2 | MA0516.2 | chr6:34191278-34191295 | GAAGGGGCGGGGCGAAG | - | 6.18 | | ZBTB18 | MA0698.1 | chr6:34193249-34193262 | TATCCAGATGTTA | + | 6.21 | | ZNF263 | MA0528.1 | chr6:34191525-34191546 | CTCCTTTCTCCTCCCTCCCCT | - | 6.01 | | ZNF263 | MA0528.1 | chr6:34191521-34191542 | CTCCCTCCTTTCTCCTCCCTC | - | 6.52 | | ZNF740 | MA0753.2 | chr6:34192046-34192059 | ACACCCCCCCCAC | + | 6.82 |
|
| | Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
| SE_15387 | chr6:34190899-34193011 | CD4_Memory_Primary_7pool | | SE_18188 | chr6:34190627-34193089 | CD4p_CD25-_CD45ROp_Memory | | SE_19450 | chr6:34191031-34191947 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_19450 | chr6:34191975-34192963 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_26784 | chr6:34190782-34192566 | Esophagus | | SE_32269 | chr6:34191136-34192580 | Gastric | | SE_32924 | chr6:34190866-34191738 | H1 | | SE_32924 | chr6:34191898-34192442 | H1 | | SE_34365 | chr6:34190859-34192745 | HCT-116 | | SE_38509 | chr6:34190839-34193085 | HUVEC | | SE_40020 | chr6:34190944-34192835 | K562 | | SE_57546 | chr6:34192000-34192434 | VACO_503 | | SE_63029 | chr6:34190859-34207435 | Tonsil | | SE_65500 | chr6:34190860-34193304 | Pancreatic_islets | | SE_68752 | chr6:34190784-34192504 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr6 | 34191726 | 34192136 | | chr6 | 34190705 | 34191000 | | chr6 | 34190903 | 34191051 | | chr6 | 34193144 | 34193230 | | chr6 | 34192400 | 34192927 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I034223 | chr6 | 34190863 | 34193565 |
|
Enhancer Sequence | TGGCTTGAGG TCAGGAGTTC GAGACCAGCC TGGGCAACAC AGTGAGACCC CTGTCTCTAC 60
AAAAAATTTA AAAACAAGCA GGCGGATCAC TTGAGGTCGG GAGTTCGAGA CCAGCCTGAC 120
CAACATGGAG AAACCCCATC TCTACTAAAA AATATAAAAT AAGCCAGGCG TGGTGGCGCA 180
GGCTTCTAAT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATCACTTGAA CCTGGGAGGC 240
AGAGGTTGCG GTGACCCAAG ATCACGCCAT TGCACTCCAG CCTGGGCAAC AAGAGTGAAA 300
CTCCGTCTCA AAAAAAAAAA AAAATTTAAA AATTAGCCAG GCCTGGTGGT GTGCACCTGT 360
AGTCCCAGCT ACCTGGGAGG CTGAGGTGGG AGGATGCTTT GAGCCTAGGA GTTCGAGGTT 420
CCAGTGAGGT TCCATCATGC CACTGCGCTC CAGCCTGGGC AAGAGAGCAA ACCCTTGTCT 480
CAAAAAACAA AAAGAGCTTT TTTAGGCTGT GCATCATTCC CCTCATGATT ATCATTTTTG 540
CCCACACCCC TATTCTTGAA GAAGCAGGAT GATGATGGTA AGAGCTGTGA TTTATTGAGC 600
ACTTAATGGA TGCTAAGTCC TGTGCTGCCT CACTTAGTGC TCACCCTGCT GTATAGCAAA 660
CAGGGCCCAG GCAGGAAATG GAATCCAACC AAAGGGTGCA AGAGGCTTTA ATGGAAGGAC 720
GACAGGGGTG GGGGCAGGGT GAAGGGGATC AACCTGGGTA TTGGGACCGG CAGTGATGAC 780
AAGACACTGC AACTTCTGGG CTGAAAGGGC AATGGGAAAA TGCAGTGTTC CCGAGCTGAC 840
ATCATGAGGG GGCATAGCCA CAGTCAGACC AAGGACCAAA ACAGGGCCAG GAGTACCCTG 900
ACTTCTCTCT CGCCTCCCCT CAGGTCGGCT GCATGGGTGC TGCTCAACAG AAAGCCAGCT 960
GGTAAGGGAG CCCGGGCCAC GAAGTCGGCA TGGGAGGGGA AGGGGCGGGG CGAAGGAAGA 1020
ATAACAAGCA TAGGGAAGCA GGATTATCCT GCTCCATGCC ATTTCGCAGA TAAGAAGACT 1080
GAGGCCCAGA GACATGAAGT AACCTGCCGG CTGCCACAGA GCTGGGAAGG TGGAGCTAGA 1140
GGAGAGCCAG GCTCTGAGGC CCTCCGCCCA GCCTCCTAAT ACAATCCCAG CCTCAAGGCG 1200
CGAGCAGAGC GCGGAGCAGG CCAGCACCCC ATGCTCCCGG TCTCCCTCCT TTCTCCTCCC 1260
TCCCCTCACT GCTCAGCTCT CCCACCCTCC CACCTTCTGT CTGCCTTAGC TGGGCCTCCC 1320
CTGGCCTCCT CTCAAGAAGG CTGTGGCCCC TTTCCTCTGT GTGCTTCCCC ACTTTGTCTC 1380
TCCCTTTTTT CTCAGTCTTC TTGTCTCCCT CACTCAGTCG CTGTCTTCAT TTCCCTCAGT 1440
CTTTCCCTAT AGCAGGCTCA CAAGGGTGCA TCCTCCTAAG GCTCAGTTTC TTTGCCATTC 1500
CCGAGCTCCG CCCCCTCTGC CCGCCGTGGC CCCGCCCCTG CCGGGCCGCC CTCCCCTGCG 1560
CTGGGCGGCG GGCCGGGTGG CAGGCGGGGG CGGGGCCCGG GCTGGCGCGG CGCCGGCCTG 1620
AGTCACACGC ATGAGGCAGC GTGAGTCAGG CGCGGAGGGA AGTCCCTGCG GAAGGGGCTT 1680
TCGGAGCTGC AGTCGAATCG CAGGGAAAGA GAAAGTGTTC GAAACGCTGC TTTGACACAG 1740
TGACCTTGTG TGAGCCCTAG CTGCACACAC CCCCCCCACC CACGCCCTCC CCGCAGACAG 1800
CAGCACGCAC ACCCCCGGCC GGCTCACGGT ACGCGGCCGC TGCCCGCACT CCCGGGTCGG 1860
GCCTGCGCGT CCCTGTGGGG TTGGGCGAGC GGGGTATCGA GGGTCCAGCA GCCTGGACCC 1920
GGCCCCTCCA CAGGGCAGTC CCTTTTCCAG CTTCCAAAAG CTAGCGTTGC TCACCTACTG 1980
CCAGACCCCA GACCCACTTC TCCCACGAGG TGTAAAGAAG GACCCCTGAG GGTCTTCCAC 2040
GTCACCTTGT GGAGCCTCGT GGAGTATGGC AGAAGGAGGA GGGCAATTTG AGGTCCTGCA 2100
GCGCCCGGGG GAACCAGGGA TGAACTCCCT CCTGCCCCCA GGCTCTCCTC CTCATCCTAG 2160
AATCAATCGA TGGGATTCAG TTACAGAAAT ATTTATTAAA CACCGACTAT ATGCCAAGTT 2220
ATAAAAACCT GGGACAAGAT GGTAAACAAA GCAGGACAGT AAACAAAATA TATTAACCCC 2280
TGCCTTTCAG GAACTGGCAT TCTAGTTAGG TGAGGGAGAT GATAAACAAA AAATAAGCAA 2340
ATGATCTAGG CTAGTGCTGC CCGATAGAAA TAGAAGGGAA GCCATGAATG TAATGTTTAA 2400
TTTTGTAGTA ACCATGTTAA GATGGTAAAA AGAAACACAT GAAATTAACT TTAATTTTTT 2460
TTTTTGAGAC CGAGTTTCGC TCTTGTTGCC CAGGCTGGAA TACAATGATG TCGACTCACC 2520
ACAACCTCTG CCTCCTGAAT TCAAGCAATT CCCCTGCCTC AGCCTCCCAA GTAGCTGGGA 2580
TTACAGGTAT TCACCACCAC TCCTGACTAA TTTTGTATTT TTGGTAGAGA TGGAGTTTCT 2640
CCATGTTGGT CAGGCTGGTC TCGAACTCCC GACCTCAGGT GATCCGCCCG CCTTGACCTC 2700
CCAAAGTGCT GGGATTACAG GCGTGAGCCA CCGCGCCTGG CCAATTTTAA TTTTTTTTTT 2760
TAAGGAACCG GGTCTTCTTA AAGGGTTCCT TAAGGAACCA GGTCTCTACT TTGTGGTCCA 2820
GGCTGGAGTT CAGTGGTGCG ATCATACCTC ACTGCGGCCT CCAACTCCTG ATGCTCCTGC 2880
CTCAGCCTTC CAAAGCCCTG AGATTACAGG CGTGAGCCAC TGGGCTTGGC CAAAATTAAC 2940
TTTAATAATG TATTCTATTT AATCCAATAT ATCCAGATGT TACCATTTCA ACATGTAATC 3000
AATATACAAA AAACTATTGA GTTTTTCTTT TTCTTTTTTC TTGTACTAAG CCTTGTAAAT 3060
CCAGTGAGTA CTTATACTTC CAGCACATTT 3090
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