Tag | Content |
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EnhancerAtlas ID | HS050-41670 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr20:31161980-31163310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR2 | MA0472.2 | chr20:31163168-31163179 | ACGCCCACGCT | + | 6.02 | FOSL2 | MA0478.1 | chr20:31162460-31162471 | ATGAGTCATCC | - | 6.62 | JUNB | MA0490.1 | chr20:31162460-31162471 | ATGAGTCATCC | - | 6.62 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_14018 | chr20:31161563-31163410 | CD34_Primary_RO01536 | SE_14522 | chr20:31161352-31164028 | CD4_Memory_Primary_7pool | SE_17373 | chr20:31161305-31164383 | CD4p_CD25-_CD45RAp_Naive | SE_18583 | chr20:31161382-31163568 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19594 | chr20:31161911-31163138 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22524 | chr20:31162102-31163256 | CD8_primiary | SE_33583 | chr20:31161380-31165717 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I032573 | chr20 | 31161714 | 31163971 |
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Enhancer Sequence | CCGCCTTCTG GATGTCCCTA CAGTGGCTCT GCCCAGTCAA GAGCCCCTGT TGCCCGGGGA 60 GACCCCTCTT CACATCCTCA TGACAATGAC AATCCCACGA GTTAAACATT TCACATGGAT 120 TCTTGCCTTT AGTTTTTCCC AACAACCTGC AGGGGAGGGG CAATCATCAC ACCCATTTTA 180 CAGACGAAGA AACTGAGGCA CCCAGTGGTT GCTTAGCTGG GGGCCCAGCA GAGCCTGTGC 240 CTTGGTTTGC TAACCTGTAG AATGGGGTCA TAACACAGCC TTGCAGGGTG CTTGAGGACT 300 GTGCAAGGCT GTGGAAGCCA GGGGCTCTCG GAAACACCCC TGAGGGCTGT CCTCAGACAA 360 GGCCGGAGGC CCGATTGTGT TTTTCTCGAC TCGCCAGCAT CCAGTCAGGG CCTGGCCTGC 420 TGAAGGAAGG GCCCCATGTC TCCTTGAACA TTTCCTCAGC CCGGGGATGC CGAGAAAACG 480 ATGAGTCATC CACCCAAGCA GAGGCCTCCC AGGAGCTTGT GTCGGGTCCC AGCCGGGAGG 540 GGAGGGCTCC AAGCTGGAGA GGGGGCCCGG GTAACACGAT GACTCCCGCG CTGGCCCCGA 600 GGCCTAAGTC ACGGGGTCCC CTCCACGGCC TCCCACCGCC ACAGGCTGCC AGCCTACCGG 660 ACACCCTTGG ATGCTGTGCC CCAGATCCTG CCCCTGCGCC TTCACCCCAG ATCTGCACCC 720 CGGTTTCCTA AACCACTCTT CCCACCCACG AATCCCAGGG TTGCCTGCGA CCCTCTAGCC 780 TCCCTCACCC CACTCCCACC TCACCTAGCC CCAGCCACTC AACCGCTGGT CCGTCGAGGA 840 AACCCGTCAC GCCTTTCTCC CCTCACCTCA CTATGCCTCT GCCTGGTTTT CCTTCTCCAT 900 CGCCCTCTTG CCTCTCACCA CAGAATCTGA GCGTTCCTTC TAAAACCCCA ACGTGACCTT 960 AGCTCCCTCC ACGTGAGAAC CCTCCTGTGA GCTCCCTGCT GTGCCTGATG CGATGGGCTC 1020 TTCAGATCTC TCTCCTCCAT CTGGCCCCAA CCAATCTTGC CAGCTCACCC CTTCAGGACC 1080 CCACTGTGGT TCTCAAGCTG ACTTGGCCAT TTACTCATCT CCACTCCATC TAGAATGTTC 1140 TTCCAAACAT GCTTCTCTAA GAAAATTGGC CCTGGGATCC GTCGTACAAC GCCCACGCTG 1200 ACCCCGCCAA AACCAGTCCC ACCCCCCGGA ATGAGCTTCC CTATGCTCTG CTCTTGCTGA 1260 AAAGTTCTTT TTGGACTTCA AGGTCCAGGT GAAATGTCAC TTTCCCAAGG ACTTCTCAGG 1320 CCCTGTCCCG 1330
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