Tag | Content |
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EnhancerAtlas ID | HS048-22134 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:219942930-219945120 |
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) |
NFAT5 | MA0606.1 | chr2:219943453-219943463 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr2:219943453-219943463 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr2:219943453-219943463 | ATTTTCCATT | + | 6.02 | Zfx | MA0146.2 | chr2:219945018-219945032 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_23646 | chr2:219942713-219945079 | Colon_Crypt_1 | SE_24654 | chr2:219943304-219943643 | Colon_Crypt_2 | SE_24654 | chr2:219943744-219944996 | Colon_Crypt_2 | SE_25299 | chr2:219942754-219945191 | Colon_Crypt_3 | SE_27657 | chr2:219942446-219945134 | Fetal_Intestine | SE_29068 | chr2:219942660-219947974 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I219078 | chr2 | 219942797 | 219945056 |
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Enhancer Sequence | GTAAGAGAGA GGAGATACTG TCATTGGTTA CACTGTATTG CTAGAGAAGC GATCTAATAC 60 CCCACATGCA GAACCGGCAT CAACCCCAAA TGAATTAATA TAAAGCAGTT AGATCCAATA 120 GGGGGCGACC ATATCCAAGC CTGGTGGCAA CCAATATAAA GATTTCTTGG GACATCTCCT 180 CTGAAGGGCA ACTCCAAATG TATATCTTAT TTCCCCTAAT CCTTAGGTCT ATTATGTTTT 240 CCCATGAATA CCCTATAGAT TTCTAGGCTC TTTTTCCAAA GGGATGATTT CTTAGAAGGC 300 TATTTTAGGA AATTATTTCC CCTAAATTTT CCCTGAGCTG AACAAATTAC TATTTTCATT 360 AAATTCATTC ATAAACTAGA GAAAAATGAT AAAATTCAGG ATAAAGGAGA GAGAGCAAAA 420 TGGTAATGAC AGACTGAGAG GCAAGAAACA ATTATGGAGC TGTGATGTTC AGGCAGAGGA 480 GACAGGAAAA ACAAAGCTGA CAAAGCTTTT GAGGCCCCCG GCCATTTTCC ATTCCCCACT 540 GCTGTCCCAC CCTCCTTTAC TATCACCCAC ATGCTCACAG TGGGCTGGCT GAGATTCCCC 600 CAAGGGAGTG AAAACTGTTC TTGAGGGGTA AAAAAAACTG ACTCTTTTAA AGTATAAAGC 660 GTGCACACAC ACACACACAG TACATAAATA GATTTTTTGG TATACCTGTG GCATTAAAAT 720 TTCCTGATAG GGAGTGATTA GGCAAAAAAT GTCTTAAAAG GTTCCTTAGG GAAGTGATAA 780 TTTTTAAAAG GCTGAGAAAC ACTGCTATGA TTACATTATA TTTATCTGTT TCCTTCACTA 840 CAGAATGAAC TGTGGACTTA CATCCACAGC AAAATACTTT GCCTAGTTGT AGTTTCATAC 900 ACTTGGCTGA ACTGCGTTGA GGTAATGGCT GAAGACTGAA CAAAGTGCGA TAAAAATGAG 960 ATGAAAGAGT AGAGTGTCTA GTGGTCCCAA ACCTGGCTGC ACTTCGGAAT CTTGGAAAGG 1020 GCCCAGAACT ATTTCACCTG TCCCTAGGCG TGCAAATCAC CATGGTTCCC AGCCAAGTTA 1080 GCAGGTCCCC AAGAGCAGCC ATGCCAGCAG CTCACATGAG AACCAACCCA AGAATCCTGG 1140 ATTGGCCCAT ACCTTGGGTC AAGGGCACCT TTTTGTGCTG TAAGGGCATT CATTTCTGAA 1200 AGCCCTCTCA TGGGAGAAGA ATAGAAGAGA GAAAGTGTGA GAAGCAGGAA AGCAGGTGCT 1260 GAACCAGTCA GGATAGCTGA AAACCTTGTT GATTACCAGG AAATGTCACA TACATTTCTA 1320 CTCCAACCCT ATCCCCACAA AGACTATATC AGGCCTGGAC TTTCACTGGA AACCACAGGC 1380 AATGAATCAG AGCCCCGAGT CCAAACTTTG CCTCTAGCCA GTAATCACAC TAGAGTCTAA 1440 CAGCCCTCTG GCAGCATTCC CTGAGGAATG AACTGAAACA GGGAAGGTAA ACTATCAGGC 1500 CACACCACCT CTACCCTACC TCACTCTCAG GAGTTCAGCT CTCTAACTCC CAAGACACCG 1560 CCTTCAAAAG AGGGTTCTCT CCTCCATAGC CAGAGAGCCC TGATGGTGGG GAGGCAAACA 1620 GCTGCCCTCC TTCCTTATAT ATTGACCTCT AGCATCTCCC TTCATACTAC CCAAGAAATG 1680 ATGCCTCTCT TAGGGTCACT CATACATGAC TTGGTAGGCA CTGTGCTGTC TACATAAATG 1740 GGTTAGGCAG AATGAGGCAG TCCAGAGTCA TTTCCTCCTG CCCTTTCCAT GGAATCAAAC 1800 AGATTCATCA ATTTTTCAGG GCGACCTTCA CTCAGCTCAA GTATTTAACC TCAAAACGAA 1860 GTGCTAGAAA TGCTGCACCT GGGTCTAAAT GTGGAACCTA ATCTAAGCCC TTCCGCTGTC 1920 CTTCCCCTTC TCAGAGAGAT CTGGTCCTGC AGTTGCTGGC AAAGTTATTC CACCTGACTA 1980 TTCTCAGAAA AGTCCTAGGA ACAGCATATT GCTAGAATTG TCGAATACTT AATATATGCT 2040 AGACATGGCC GGGCATGGTG GCTCACACCT GTAATCCCAG CACTTTGGGA GGCCGAGGCG 2100 GGCGGATCAC AACGTCAGGA GAACGAGACC ACGGTGAAAC CGCATCTCTA CTAAAAAAGA 2160 CAAAAAATTA GCCGGGCACG GTGGTGGGCG 2190
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