| Tag | Content |
|---|
EnhancerAtlas ID | HS088-45123 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr6:34190360-34193410 |
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 | GGCGGATCAC TTGAGGTCGG GAGTTCGAGA CCAGCCTGAC CAACATGGAG AAACCCCATC 60
TCTACTAAAA AATATAAAAT AAGCCAGGCG TGGTGGCGCA GGCTTCTAAT CCCAGCTACT 120
CGGGAGGCTG AGGCAGGAGA ATCACTTGAA CCTGGGAGGC AGAGGTTGCG GTGACCCAAG 180
ATCACGCCAT TGCACTCCAG CCTGGGCAAC AAGAGTGAAA CTCCGTCTCA AAAAAAAAAA 240
AAAATTTAAA AATTAGCCAG GCCTGGTGGT GTGCACCTGT AGTCCCAGCT ACCTGGGAGG 300
CTGAGGTGGG AGGATGCTTT GAGCCTAGGA GTTCGAGGTT CCAGTGAGGT TCCATCATGC 360
CACTGCGCTC CAGCCTGGGC AAGAGAGCAA ACCCTTGTCT CAAAAAACAA AAAGAGCTTT 420
TTTAGGCTGT GCATCATTCC CCTCATGATT ATCATTTTTG CCCACACCCC TATTCTTGAA 480
GAAGCAGGAT GATGATGGTA AGAGCTGTGA TTTATTGAGC ACTTAATGGA TGCTAAGTCC 540
TGTGCTGCCT CACTTAGTGC TCACCCTGCT GTATAGCAAA CAGGGCCCAG GCAGGAAATG 600
GAATCCAACC AAAGGGTGCA AGAGGCTTTA ATGGAAGGAC GACAGGGGTG GGGGCAGGGT 660
GAAGGGGATC AACCTGGGTA TTGGGACCGG CAGTGATGAC AAGACACTGC AACTTCTGGG 720
CTGAAAGGGC AATGGGAAAA TGCAGTGTTC CCGAGCTGAC ATCATGAGGG GGCATAGCCA 780
CAGTCAGACC AAGGACCAAA ACAGGGCCAG GAGTACCCTG ACTTCTCTCT CGCCTCCCCT 840
CAGGTCGGCT GCATGGGTGC TGCTCAACAG AAAGCCAGCT GGTAAGGGAG CCCGGGCCAC 900
GAAGTCGGCA TGGGAGGGGA AGGGGCGGGG CGAAGGAAGA ATAACAAGCA TAGGGAAGCA 960
GGATTATCCT GCTCCATGCC ATTTCGCAGA TAAGAAGACT GAGGCCCAGA GACATGAAGT 1020
AACCTGCCGG CTGCCACAGA GCTGGGAAGG TGGAGCTAGA GGAGAGCCAG GCTCTGAGGC 1080
CCTCCGCCCA GCCTCCTAAT ACAATCCCAG CCTCAAGGCG CGAGCAGAGC GCGGAGCAGG 1140
CCAGCACCCC ATGCTCCCGG TCTCCCTCCT TTCTCCTCCC TCCCCTCACT GCTCAGCTCT 1200
CCCACCCTCC CACCTTCTGT CTGCCTTAGC TGGGCCTCCC CTGGCCTCCT CTCAAGAAGG 1260
CTGTGGCCCC TTTCCTCTGT GTGCTTCCCC ACTTTGTCTC TCCCTTTTTT CTCAGTCTTC 1320
TTGTCTCCCT CACTCAGTCG CTGTCTTCAT TTCCCTCAGT CTTTCCCTAT AGCAGGCTCA 1380
CAAGGGTGCA TCCTCCTAAG GCTCAGTTTC TTTGCCATTC CCGAGCTCCG CCCCCTCTGC 1440
CCGCCGTGGC CCCGCCCCTG CCGGGCCGCC CTCCCCTGCG CTGGGCGGCG GGCCGGGTGG 1500
CAGGCGGGGG CGGGGCCCGG GCTGGCGCGG CGCCGGCCTG AGTCACACGC ATGAGGCAGC 1560
GTGAGTCAGG CGCGGAGGGA AGTCCCTGCG GAAGGGGCTT TCGGAGCTGC AGTCGAATCG 1620
CAGGGAAAGA GAAAGTGTTC GAAACGCTGC TTTGACACAG TGACCTTGTG TGAGCCCTAG 1680
CTGCACACAC CCCCCCCACC CACGCCCTCC CCGCAGACAG CAGCACGCAC ACCCCCGGCC 1740
GGCTCACGGT ACGCGGCCGC TGCCCGCACT CCCGGGTCGG GCCTGCGCGT CCCTGTGGGG 1800
TTGGGCGAGC GGGGTATCGA GGGTCCAGCA GCCTGGACCC GGCCCCTCCA CAGGGCAGTC 1860
CCTTTTCCAG CTTCCAAAAG CTAGCGTTGC TCACCTACTG CCAGACCCCA GACCCACTTC 1920
TCCCACGAGG TGTAAAGAAG GACCCCTGAG GGTCTTCCAC GTCACCTTGT GGAGCCTCGT 1980
GGAGTATGGC AGAAGGAGGA GGGCAATTTG AGGTCCTGCA GCGCCCGGGG GAACCAGGGA 2040
TGAACTCCCT CCTGCCCCCA GGCTCTCCTC CTCATCCTAG AATCAATCGA TGGGATTCAG 2100
TTACAGAAAT ATTTATTAAA CACCGACTAT ATGCCAAGTT ATAAAAACCT GGGACAAGAT 2160
GGTAAACAAA GCAGGACAGT AAACAAAATA TATTAACCCC TGCCTTTCAG GAACTGGCAT 2220
TCTAGTTAGG TGAGGGAGAT GATAAACAAA AAATAAGCAA ATGATCTAGG CTAGTGCTGC 2280
CCGATAGAAA TAGAAGGGAA GCCATGAATG TAATGTTTAA TTTTGTAGTA ACCATGTTAA 2340
GATGGTAAAA AGAAACACAT GAAATTAACT TTAATTTTTT TTTTTGAGAC CGAGTTTCGC 2400
TCTTGTTGCC CAGGCTGGAA TACAATGATG TCGACTCACC ACAACCTCTG CCTCCTGAAT 2460
TCAAGCAATT CCCCTGCCTC AGCCTCCCAA GTAGCTGGGA TTACAGGTAT TCACCACCAC 2520
TCCTGACTAA TTTTGTATTT TTGGTAGAGA TGGAGTTTCT CCATGTTGGT CAGGCTGGTC 2580
TCGAACTCCC GACCTCAGGT GATCCGCCCG CCTTGACCTC CCAAAGTGCT GGGATTACAG 2640
GCGTGAGCCA CCGCGCCTGG CCAATTTTAA TTTTTTTTTT TAAGGAACCG GGTCTTCTTA 2700
AAGGGTTCCT TAAGGAACCA GGTCTCTACT TTGTGGTCCA GGCTGGAGTT CAGTGGTGCG 2760
ATCATACCTC ACTGCGGCCT CCAACTCCTG ATGCTCCTGC CTCAGCCTTC CAAAGCCCTG 2820
AGATTACAGG CGTGAGCCAC TGGGCTTGGC CAAAATTAAC TTTAATAATG TATTCTATTT 2880
AATCCAATAT ATCCAGATGT TACCATTTCA ACATGTAATC AATATACAAA AAACTATTGA 2940
GTTTTTCTTT TTCTTTTTTC TTGTACTAAG CCTTGTAAAT CCAGTGAGTA CTTATACTTC 3000
CAGCACATTT CAGCTCAGCC TGAACACATT CCCAGCACTC AGTGGCCACA 3050
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