| Tag | Content |
|---|
EnhancerAtlas ID | HS187-18246 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:2786610-2789740 |
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 | | Nr2f6(var.2) | MA0728.1 | chr4:2786718-2786733 | TGAACTCCTGACCTC | - | 6.22 | | 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 | | Zfx | MA0146.2 | chr4:2786743-2786757 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 | CTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGACATGTG CCACCATGCC AGGCTACTTT 60
TGTATTTTTA GTAGACATGG CATTTCACCA TGTTGGCCAG GCTGGTCTTG AACTCCTGAC 120
CTCTGGTGAT CCACCCGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TAAGCCACCA 180
CGCCCGTCCA ACTGTAGTTC TAAATCACCA TCATGTTCCA AAGAAAGACT GACCAACGGG 240
ACTTGAATGC TGTAGAACAG TCTTCATTGC CTGAACTTTG AATTGTTCGG TTTTGATCCG 300
TTTGGTTCAC CGAGCCTCCT GTTAAGGAGT GTGCTTCAGT TTCTTGTATC ATCCTCCCAA 360
AAGCCGTCAG AACAGTCTCT CTGATACGCT GTCCCCTCAA GTGTCTTAAA TGCTTGTATG 420
CAGCCATCCT TAGTACATCA AATGGTCTCA TCACAGTTAG AGGAACAAAA CATGAAGAAA 480
ACATCATCAT CCAACTAACT TGACACGGTG AATATGAATT TCACACTGAG ACCAAACAAA 540
TCCATTATGA TGGTGACAGA AAGTGACGCC AGTGCCCAAG GTTTCAGTCA ATCTCTCAAA 600
ATTGAGAGGC TGCCTAAAAG AGGCAAAGGT TAAATTAACT TAAATTTGGC CTAAAGCTGC 660
CTCAGCATAT GGCAAACCCT AACCTGCCTT AATCTGTAAA TAAACTGCAG CCTGGGAGTA 720
TACTCAAGCT GCAGTTTGTT TACAGATTAA GTCAGGTTAG GGTTTGCTAT AGTCACAGGA 780
CTCTTTGGAA GAAGTCACTG AGTCTCGGCC CATCAGAGCA GCTGAGCTTT CAGCCAGTCA 840
CAGGCTGCAA ACTACTCAGG CAGGTTCAAA GAAGGCAAGC ACCCAGTTGT AGCCAATCAG 900
ACGATTTCTG TGTCACTTCC TTTTTCTGTC CATAAATACT GCCTGCCCAA GTTGCTGGAT 960
GGAGCTCTCT GAGCCTCTAC TGGTTCGGGG TGCTGCCTGA TTTAGGAATC ATTTCATTGC 1020
TCAAATAAAC TCTGCTAAAT TGAATTCATC TAAAGTGTTT CTTTTCTATT TTTCTTTTCT 1080
TTTTCTTTTT TTTTTTTTTT TTTGAGACAG AATCTCGCTC TTGCCCAGGC TGGAGTGCAG 1140
TGGCACCATC TCGGCTCACT GCAACCTCTA CCTCCCGGGT TCAAGTGACT CTCCTGCCTC 1200
AGCCTCCCAA GTAGCTGGGA TTACAGGCAT GTGCTACCAC ACCTGGCTAA TTTGTGTGTT 1260
TTTAGTGGAG ACTGGGTTTC ACCATGTTGG CCAGGCTGCT AAGTAGCTTC AGGGACGAGA 1320
AGGTGTAAGG ATGTGAAAAG CACCTGGTAC TGTACCTGGC ACAGCAGGTA CTCCAGGAGG 1380
GCTGAGGGTG TGCACATCCC TGACTGGGCC TCACACCATC ACAGGCCAGA CCTTGTTCAG 1440
CTCTGCGTCA GCACCTACCC CCCCACTCCC CTGCCGCCTC TTCAGTGTGA TGGGAAAGTC 1500
CCCACCCTTG GGGTCCTGAG TCTTCTGCTG TTCCCGCCAG CTCTGGGCTG GGTGGGGCAG 1560
CTCATCTTTC CAGCTTCACC CCCTGTCAGA GGCCGGGAGG AGGGGCAGTG CAGGCTGGGG 1620
GCTCAGAGAC AGGGCTACTG GGCCAGAGCC ATTCTGAGCT ACTTGGTGGG CCCCAGTATC 1680
ACCGCCGATA GAACCCCACC CTCCACAGGC TCACTGAGGG CAGCTGGCCA CTCCTGACCC 1740
TGGGCTGGGC ACATCAGGGG TGCCCCTGAG TGGAGAGGTG GCACTGTAGG GCATCACAGT 1800
GTTGGGGGTT CGCACATAAG AGCCCATGTC ATCGGGGAGA GGGTGGCACT TTGGGGAGGG 1860
GTGTTCTCAG GGCCGTAGCA GGGGCCTTTA GGGCTGCCAG CATGGTTTAG GGGACCCACA 1920
AGTGTGGAAT TAAGGCCAAG GTCCACTCCC AAGGATGGAG AAGTGGAAGG GGGAGGGAGT 1980
GGTCCTCTGG GTCCTCGGCT GGGCAGGCGG CTGAAGGCCT GGTGAGACCC CTTCAGAACC 2040
CACTTGAGGC CAGGTGGGAC GGGGAGTTCT GGGTCCCAGT GGGGCGAGTC CCTCATTCAC 2100
TCCTGCCAAG GCAGCCCAGT CCTGCCACGG CCATGGGAGA GGCCTGGGGA GTCGAGGTGG 2160
GAGCAGCCCT CAAGTGTCTC CTGGGGTCCC CTCTCCCAGG AGGCCTCCCA GGCTCATCTG 2220
TTCTCTTGTT CCTTCCTGCT CTGGTCGTGA GGGGCTTTGC TGTCACGCAG GTCACCTTGC 2280
ACCCTCATGT CTCAGTGTCC AGCGCTGGCT GGGGAAGGGC TGGCTGCCTC TCCTGACCCT 2340
GGGCTGGGGT GATAGGTGGG GACCCCTTGG GGTGACGTGG GAACCTCACC ACTGTTGAAG 2400
GCCACAGCTT CCCCTTCCCA AGCCCCACAT GGGCTTCCCC TTCCAGATCT CAGTGTGTTC 2460
CTGAAGGTCA CGTGGCTGGC AGGGGGTGGT GGTGGGGGTG GGGGGTGACA GGAGAGGGGG 2520
TGTTTTGGAG GGAGGCGGGT GGGGCACGCT GTTGTGTACA AACACCCACC TCCCACGGCA 2580
CAGGGGCCGG AAGTGGCCCC AGAATAGAAT GTGCTGCTTT CAAGTTCCAA ATTGGGCTCT 2640
GGGGGTGAGA GCAGGCGACT CTGGATGTAA AAATAGAAAA GCCAGTGCGT GCGTGGGTCC 2700
TGGGTCCTCC ACCCACAGGC CTGGTATTAC AAAATAGAGC TTCCTAATGG GACCTGCCTG 2760
ACACTCTCGT TTTATGTAGA AAATTGACTC AAGCAAACCT CAGAGGACAG AGCCAGCAGC 2820
TGACCTGGGC TAGAGGTGTG GCAGCCAGGC AGGCAGGGCA GGCCCTCCTG GGGAGTGCTG 2880
GTGGCCTGGG GGCGCTGGCT GGCCCTTGAC CTGGCGTGAA CTCTGGCTCT ATTTCCCTCA 2940
CTCTGCCCTC TAGCGCTGTG CCCCTGCCAG GAGAGTCCTC CCAGGTTGTG GGAGCCCAGC 3000
TCAGTCCTAC TGTCCCCAAA GAGCCTTCGC CGACTTCGTC AGCCTTTACC AGCTCTCAGG 3060
CTGGCCAGGA AGCCAGGCCT GTCCCAGGCA CGAGGGGCAG TGGGCAAGCT GGCTGTGGGC 3120
CCCACCCTCC 3130
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