Tag | Content |
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EnhancerAtlas ID | HS187-22511 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:29324430-29325790 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr7:29325192-29325207 | AGTGCTGACTCATAC | - | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_04956 | chr7:29323688-29325844 | Brain_Cingulate_Gyrus | SE_60318 | chr7:29309085-29339482 | Ly4 | SE_63452 | chr7:29310842-29333310 | NCI-H69 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 29324852 | 29325382 | chr7 | 29325062 | 29325307 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I029284 | chr7 | 29324501 | 29325832 |
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Enhancer Sequence | GTTCTGTAGC AATAACAGAT GAATGCACAA GGATCTGAAC CTCGTGATTC TGGCTGCAGA 60 GCTCACATGC ATCCTCCCTT CTCCAGGCAG CCTCTTCAGA GACGTCATCT CAAAAATCAC 120 TAAATCCTGG AACTTCAGGG TTGAATGGGG AACTTTGATC TAGCCCAGTT GTTTAATCAA 180 ACTTTTCCTT TGCAGCAGAT GGCCACTGTG CAAGCAGACT GGGGGAGCTG CTCTACTTGC 240 TGTGGGGTGT GTGAGCCGCT TCTGTTCTTT GCACTCCTCT CCTTGAGGAA TCTCTGGGGA 300 ACACAGTTTG AGAACCACTG ATCTGATCCA ACAACTCATC TTTACATTTC CCTCTACAAC 360 ATCCTGACAC CTTGTTCCTT TGGAAAGTCT TCTGTGGCAT TGAAATCTGG CTCACCGTAA 420 TTCCCACTAT TGGTCCAGGT CCAGTCATAG GTGATACACA GAGCAAATGG AACTCTTTTT 480 CCATAGGAGA ATGCATCACT CATTAAAGAC AGTTCTCACG TTTCATGGAA GCCTTCTATT 540 TTCCAGACAA AACATCTCCA TGACCACAAA GGAGCTGCCA GTCCCTTCTC TCCTAGTGTT 600 TGCCTGTGTT TCTCTTAGAG TCAGGTCAGG AACTAAGCAC AAAATTTTTG GTGTGGTCTG 660 CTTCACATAA AATACGGCAA GCCTAGCATA AGCCACAGTC TAAATATTCT GTTTCCATGA 720 ATGCAGCGTT AGACCACATT TGCTTTTTCG CAACCACAAT GCAGTGCTGA CTCATACCAC 780 ACGCAGAGTC AATCAAAATT CCCTTTTCAC ATATGTGGTT GCTAGGGTAT GTCTTCACCA 840 ACATGTACTT AGGTGTGTTT ATTTTAACCT GAATACAGGC TTCACATTCA TCACCATTGT 900 GTCTCATCAG GGATCTGGTG CATATCTTGG ATGATCCTGA TTATGTCATC CAACAATATT 960 GCTCTTCTCC CTAGCATCAC CTCAACTCTC AATTGGACAA ATATGCCATA AATATCCTCA 1020 TCGGAGTTAT TGACAGAATT TTGGAACCAG ACAGGGCTGA GGTCAGAGCC CTCTAGCACC 1080 ATATTGATGA CTATTCCCAG TGTTTGGGTC CTTCAAAAAC TTACAAATCC AACTAATTGT 1140 ATCATCTAAT GGCAGTGATC CAACTCATAA AGGTACCACC AGAAACATAA TGAACTATTT 1200 CCTGGCCGCC AAGTACAGGC ATTAAGTCCA TTTCTCTGCC TTCCCAAGCC AGGAGGTCAC 1260 TAGAGCTCCT CCTGCATGCC CACAAACATG TAGGAGCCTC TTTTCGAGGA TGTGCCTCAT 1320 ACCCACCCTT TTATAGTTTG CTCCTCCTTA GATAAACACC 1360
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