Tag | Content |
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EnhancerAtlas ID | HS180-40562 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr5:173205070-173206520 |
SNPs | Number: 3 | 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 | chr5:173205866-173205881 | AAGTGACTCAGCATA | + | 6.55 | Nfe2l2 | MA0150.2 | chr5:173205864-173205879 | AGAAGTGACTCAGCA | + | 6.16 | ZNF263 | MA0528.1 | chr5:173205918-173205939 | TGAGGAGGAGGAAAAGGAGTG | + | 6.83 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_01236 | chr5:173205832-173206303 | Adrenal_Gland | SE_27986 | chr5:173204852-173206829 | Fetal_Intestine | SE_28759 | chr5:173204743-173206901 | Fetal_Intestine_Large | SE_34749 | chr5:173204578-173211027 | HeLa | SE_38832 | chr5:173204484-173206689 | HUVEC | SE_61346 | chr5:173159769-173218323 | HBL1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I173777 | chr5 | 173204067 | 173211450 |
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Enhancer Sequence | GCAGCTGGGG GCTCTAGGTC CATCCCTGCC CTCCCCGAAG CAGGAGAGTA ACCTTGTAGA 60 CTTCCTGTTA GGGCCCTGGG GTCTCTGGGT GAATTTGATG CAGACTCAGC CATTAGCCTG 120 GCTGGGCCAC AAAATCAGGA AGCTTAGACC AGTGTTGTGG AACCTTGATT CCTGTCCCAG 180 TTTTGTCATT TCCTGCCTCA GCCTCTTTGC AACTCCCGGC CTCAATTGCC TCACCTCCAA 240 AATGGAGGTC TTAATGACAA TGGTCTGGCT TCACTCACAG GGTTATCGTG AAAATCAAAA 300 GAGATTGCTC AGGGAAAAGC CTCTTCAAAC TGGAGCTCCA GGTGATGGTT GTCATCTGTC 360 GATGTTGCTC TCTGGTGAGT TCTTTAAAAA TGGAAATTAC TGTTTGTTTC TAATTACAAA 420 AGTTCAGGAG TTACAGAATA GCACACAGAT TTTTAAACAC GGTTTATTAC CCCACTACTT 480 GTTAATAATC TCTACTAACC TGTTGGTGTA TTTCCTTCCG GATACATAAA GAGAGTTGAA 540 CCCTGAACGA TATGGAAGTT GGGGTGTTGA CCCCCCTCAG AGTTGAAAAT CTGCATACAA 600 CTTTTGACTC CCCAAAACAC TACAGATAGC CTACTGTTGA CTGCAAGCCT TGCTGAGAAC 660 ATAAACAGTC AATTAACATA TTTTGTATGT TATATGTATT GTATACTGTA TTCTTACAAT 720 AAAGGAAGCT AGAGTAAAGA AAATGTTATT GAGAAAATCA TAAGGAAGAG AAAGTATATT 780 TACGTTCACT ACGCAGAAGT GACTCAGCAT AAAGGTCTTC ACCCTTGTCA TCATCAACTC 840 GAGTAGGCTG AGGAGGAGGA AAAGGAGTGG TTGGTCCTGC TCTCTCAGGG GTGGCAGAGG 900 TGGAAGAAAA GTCACCTGTA AGTGGACCTG TGCAGTTCAA ACCTGTGTTG TTTGAAGGTC 960 AACTGTATGA TGATTGCCTA CATAGAACCC GGTAGCTTTC TACAGCACTT GGAAGGAAAT 1020 CCACACTCCT TATCAACACT TCACCTTGAC TTTCAGTCTG TGTGATCTGG CCCTGCTTGC 1080 CTCTCCTACC TCTTCTCTCT CTACTCACAC ATTATTTCTC TTTCTTTTTC CCTCCTAATA 1140 CACCAATGGC ATTTCCCCTC AAGGCCTTCG CCTCTTTGCC TGAAATGCTC TGGATTTCAT 1200 GACTCTGGAA ATCATGACTG GATTTTTTTT TTTTCAGCGT GCAAGTCATG GCCGAAATGT 1260 CACCTCCTTG GATAGTCCCT CCATCTTCAC GCACACTAAA CTAGTCCATC TTGCATGCCT 1320 TTCTTCATGG CATTGTGTGC CATGCTCAGA AATTATCTTG TGTATTCTTA AGTCCATATA 1380 TGTATTACCT GTCTTTCCCT AAACAACTTC CCACCCTGAG CTTGTTCCTG TCCATATTCC 1440 CAGTACCCAG 1450
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