| Tag | Content |
|---|
EnhancerAtlas ID | HS051-20671 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr4:2787050-2789740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK4 | MA0076.2 | chr4:2789195-2789206 | GCCGGAAGTGG | - | 6.62 | | Gabpa | MA0062.2 | chr4:2789196-2789207 | CCGGAAGTGGC | + | 6.62 | | MAFK | MA0496.2 | chr4:2787261-2787280 | TAAAGCTGCCTCAGCATAT | - | 6.02 | | NFYA | MA0060.3 | chr4:2787500-2787511 | AGCCAATCAGA | + | 6.32 | | RREB1 | MA0073.1 | chr4:2789093-2789113 | GGGTGGTGGTGGGGGTGGGG | - | 6.06 | | RREB1 | MA0073.1 | chr4:2789120-2789140 | GGAGAGGGGGTGTTTTGGAG | - | 6.55 | | USF1 | MA0093.2 | chr4:2789075-2789086 | GGTCACGTGGC | - | 6.62 | | USF2 | MA0526.2 | chr4:2789072-2789088 | GAAGGTCACGTGGCTG | + | 6.44 | | ZBTB7A | MA0750.2 | chr4:2789194-2789207 | GGCCGGAAGTGGC | + | 7.04 | | ZNF263 | MA0528.1 | chr4:2788563-2788584 | GATGGAGAAGTGGAAGGGGGA | + | 6.06 | | ZNF263 | MA0528.1 | chr4:2788566-2788587 | GGAGAAGTGGAAGGGGGAGGG | + | 6.32 |
|
| | Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
| SE_09219 | chr4:2786593-2791007 | CD14 | | SE_10351 | chr4:2786830-2791603 | CD19_Primary | | SE_11326 | chr4:2786410-2796453 | CD20 | | SE_22654 | chr4:2786826-2791087 | CD8_primiary | | SE_24078 | chr4:2788189-2789107 | Colon_Crypt_2 | | SE_24078 | chr4:2789288-2789846 | Colon_Crypt_2 | | SE_24900 | chr4:2788070-2789176 | Colon_Crypt_3 | | SE_24900 | chr4:2789277-2790629 | Colon_Crypt_3 | | SE_27350 | chr4:2789146-2789983 | Esophagus | | SE_31839 | chr4:2787784-2790022 | Gastric | | SE_42466 | chr4:2787811-2789128 | Lung | | SE_42466 | chr4:2789139-2790922 | Lung | | SE_48033 | chr4:2788590-2789018 | Pancreas | | SE_50306 | chr4:2787606-2790913 | Sigmoid_Colon | | SE_53128 | chr4:2787805-2790877 | Small_Intestine | | SE_53322 | chr4:2787781-2790565 | Spleen | | SE_60153 | chr4:2786744-2817100 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 2787129 | 2789491 | | chr4 | 2788284 | 2789696 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I002785 | chr4 | 2787014 | 2791292 |
|
Enhancer Sequence | AATGGTCTCA TCACAGTTAG AGGAACAAAA CATGAAGAAA ACATCATCAT CCAACTAACT 60
TGACACGGTG AATATGAATT TCACACTGAG ACCAAACAAA TCCATTATGA TGGTGACAGA 120
AAGTGACGCC AGTGCCCAAG GTTTCAGTCA ATCTCTCAAA ATTGAGAGGC TGCCTAAAAG 180
AGGCAAAGGT TAAATTAACT TAAATTTGGC CTAAAGCTGC CTCAGCATAT GGCAAACCCT 240
AACCTGCCTT AATCTGTAAA TAAACTGCAG CCTGGGAGTA TACTCAAGCT GCAGTTTGTT 300
TACAGATTAA GTCAGGTTAG GGTTTGCTAT AGTCACAGGA CTCTTTGGAA GAAGTCACTG 360
AGTCTCGGCC CATCAGAGCA GCTGAGCTTT CAGCCAGTCA CAGGCTGCAA ACTACTCAGG 420
CAGGTTCAAA GAAGGCAAGC ACCCAGTTGT AGCCAATCAG ACGATTTCTG TGTCACTTCC 480
TTTTTCTGTC CATAAATACT GCCTGCCCAA GTTGCTGGAT GGAGCTCTCT GAGCCTCTAC 540
TGGTTCGGGG TGCTGCCTGA TTTAGGAATC ATTTCATTGC TCAAATAAAC TCTGCTAAAT 600
TGAATTCATC TAAAGTGTTT CTTTTCTATT TTTCTTTTCT TTTTCTTTTT TTTTTTTTTT 660
TTTGAGACAG AATCTCGCTC TTGCCCAGGC TGGAGTGCAG TGGCACCATC TCGGCTCACT 720
GCAACCTCTA CCTCCCGGGT TCAAGTGACT CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA 780
TTACAGGCAT GTGCTACCAC ACCTGGCTAA TTTGTGTGTT TTTAGTGGAG ACTGGGTTTC 840
ACCATGTTGG CCAGGCTGCT AAGTAGCTTC AGGGACGAGA AGGTGTAAGG ATGTGAAAAG 900
CACCTGGTAC TGTACCTGGC ACAGCAGGTA CTCCAGGAGG GCTGAGGGTG TGCACATCCC 960
TGACTGGGCC TCACACCATC ACAGGCCAGA CCTTGTTCAG CTCTGCGTCA GCACCTACCC 1020
CCCCACTCCC CTGCCGCCTC TTCAGTGTGA TGGGAAAGTC CCCACCCTTG GGGTCCTGAG 1080
TCTTCTGCTG TTCCCGCCAG CTCTGGGCTG GGTGGGGCAG CTCATCTTTC CAGCTTCACC 1140
CCCTGTCAGA GGCCGGGAGG AGGGGCAGTG CAGGCTGGGG GCTCAGAGAC AGGGCTACTG 1200
GGCCAGAGCC ATTCTGAGCT ACTTGGTGGG CCCCAGTATC ACCGCCGATA GAACCCCACC 1260
CTCCACAGGC TCACTGAGGG CAGCTGGCCA CTCCTGACCC TGGGCTGGGC ACATCAGGGG 1320
TGCCCCTGAG TGGAGAGGTG GCACTGTAGG GCATCACAGT GTTGGGGGTT CGCACATAAG 1380
AGCCCATGTC ATCGGGGAGA GGGTGGCACT TTGGGGAGGG GTGTTCTCAG GGCCGTAGCA 1440
GGGGCCTTTA GGGCTGCCAG CATGGTTTAG GGGACCCACA AGTGTGGAAT TAAGGCCAAG 1500
GTCCACTCCC AAGGATGGAG AAGTGGAAGG GGGAGGGAGT GGTCCTCTGG GTCCTCGGCT 1560
GGGCAGGCGG CTGAAGGCCT GGTGAGACCC CTTCAGAACC CACTTGAGGC CAGGTGGGAC 1620
GGGGAGTTCT GGGTCCCAGT GGGGCGAGTC CCTCATTCAC TCCTGCCAAG GCAGCCCAGT 1680
CCTGCCACGG CCATGGGAGA GGCCTGGGGA GTCGAGGTGG GAGCAGCCCT CAAGTGTCTC 1740
CTGGGGTCCC CTCTCCCAGG AGGCCTCCCA GGCTCATCTG TTCTCTTGTT CCTTCCTGCT 1800
CTGGTCGTGA GGGGCTTTGC TGTCACGCAG GTCACCTTGC ACCCTCATGT CTCAGTGTCC 1860
AGCGCTGGCT GGGGAAGGGC TGGCTGCCTC TCCTGACCCT GGGCTGGGGT GATAGGTGGG 1920
GACCCCTTGG GGTGACGTGG GAACCTCACC ACTGTTGAAG GCCACAGCTT CCCCTTCCCA 1980
AGCCCCACAT GGGCTTCCCC TTCCAGATCT CAGTGTGTTC CTGAAGGTCA CGTGGCTGGC 2040
AGGGGGTGGT GGTGGGGGTG GGGGGTGACA GGAGAGGGGG TGTTTTGGAG GGAGGCGGGT 2100
GGGGCACGCT GTTGTGTACA AACACCCACC TCCCACGGCA CAGGGGCCGG AAGTGGCCCC 2160
AGAATAGAAT GTGCTGCTTT CAAGTTCCAA ATTGGGCTCT GGGGGTGAGA GCAGGCGACT 2220
CTGGATGTAA AAATAGAAAA GCCAGTGCGT GCGTGGGTCC TGGGTCCTCC ACCCACAGGC 2280
CTGGTATTAC AAAATAGAGC TTCCTAATGG GACCTGCCTG ACACTCTCGT TTTATGTAGA 2340
AAATTGACTC AAGCAAACCT CAGAGGACAG AGCCAGCAGC TGACCTGGGC TAGAGGTGTG 2400
GCAGCCAGGC AGGCAGGGCA GGCCCTCCTG GGGAGTGCTG GTGGCCTGGG GGCGCTGGCT 2460
GGCCCTTGAC CTGGCGTGAA CTCTGGCTCT ATTTCCCTCA CTCTGCCCTC TAGCGCTGTG 2520
CCCCTGCCAG GAGAGTCCTC CCAGGTTGTG GGAGCCCAGC TCAGTCCTAC TGTCCCCAAA 2580
GAGCCTTCGC CGACTTCGTC AGCCTTTACC AGCTCTCAGG CTGGCCAGGA AGCCAGGCCT 2640
GTCCCAGGCA CGAGGGGCAG TGGGCAAGCT GGCTGTGGGC CCCACCCTCC 2690
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