| Tag | Content |
|---|
EnhancerAtlas ID | HS180-27263 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr2:127841320-127843970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr2:127842205-127842216 | AGAGATAAGAA | - | 6.32 | | Gata1 | MA0035.3 | chr2:127842205-127842216 | AGAGATAAGAA | - | 6.32 | | KLF5 | MA0599.1 | chr2:127842613-127842623 | GCCCCGCCCC | + | 6.02 | | Zfx | MA0146.2 | chr2:127843341-127843355 | CAGGCCTCAGCCCC | - | 6.21 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_00572 | chr2:127838207-127846198 | Adipose_Nuclei | | SE_00914 | chr2:127837091-127843980 | Adrenal_Gland | | SE_03157 | chr2:127840812-127842608 | Brain_Angular_Gyrus | | SE_03157 | chr2:127842878-127844118 | Brain_Angular_Gyrus | | SE_03883 | chr2:127821506-127844236 | Brain_Anterior_Caudate | | SE_04777 | chr2:127820278-127857314 | Brain_Cingulate_Gyrus | | SE_05775 | chr2:127806116-127867885 | Brain_Hippocampus_Middle | | SE_06689 | chr2:127821297-127857092 | Brain_Hippocampus_Middle_150 | | SE_07740 | chr2:127821073-127849400 | Brain_Inferior_Temporal_Lobe | | SE_08942 | chr2:127842192-127842509 | Brain_Mid_Frontal_Lobe | | SE_19824 | chr2:127842348-127843293 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_22831 | chr2:127841008-127845265 | CD8_primiary | | SE_24390 | chr2:127841733-127843718 | Colon_Crypt_2 | | SE_29563 | chr2:127836160-127857245 | Fetal_Muscle | | SE_31713 | chr2:127837676-127844066 | Gastric | | SE_36991 | chr2:127828440-127865759 | HSMMtube | | SE_41757 | chr2:127841273-127843893 | LNCaP | | SE_48048 | chr2:127806769-127857236 | Psoas_Muscle | | SE_50749 | chr2:127840740-127843883 | Sigmoid_Colon | | SE_51095 | chr2:127817891-127857315 | Skeletal_Muscle | | SE_54239 | chr2:127840923-127843925 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I127071 | chr2 | 127828680 | 127857094 |
|
Enhancer Sequence | TGTTATCCAT TTTTTTTCTT TCGTGATACT GGTATCTTTT TAAGAGTGCA AACCAATCAC 60
TTGGAGAATG CCCCACACTC TGGATCCATC TGATTGTTTC CTTGTGAGGA AGTTCAGGTT 120
AAAGGCTGCT TTGGCAAGAG TCCTGCAGAG GGAGGCTGAG CCTTCCCACC GCACCACAGC 180
TGTGTTAGGC TTGACCGCCG GGTCTGAGTC GTGTTTGCCA GATCTCTTGG AAAGGAAGGT 240
CACTTTTCTC TTAGTCATCT GCAGGACAAT CACGGTCACT GTGGCAAGGC AAAAAGTTGT 300
TGAAATTTTT GCACAGTGCC TTTACTATCC ATCATTCTTT GCTATTCAGT GTGAGGTCTG 360
TGGGCAGCTG CATGACAGTC TTCCAAGAGC CTGGAGGAGA AAAAAAACTG CAGACCTGCT 420
GAACCAGAGT GTTCCCTTTA ACAAGTCCCC CTGGCGCACC GTATGCGCAG TGAAGTCTGA 480
GAAGCACTGC AATAGCATCT TGGCTGGAAC CCGCTGTTAC CCAATCTCCT CCACGTGACC 540
CGGCATTCCA CAAACACGAG CCTCCCCTGG TCTTGCCTTT GCGAGGAGGG TGGTGAGGAT 600
ATCGTGAGTC CTTCGTTTTG CGTTCGTGAT TCATTTTGAT GCTCAAACAT CCCAAGTGCG 660
ACCAGTGGGA GGTTTCGGAC ACGTCCTCAT TCATCTCCAG GCGCTTCCTT ACTTTCTGGC 720
ACTAGCAGAT TCTCCAGGCT CAGCCTGCAC TGTCCCTGCC CCAGCCCTGG CATCAGCCAT 780
TTCTCCAAGG AACCCTGATT TCCTTCGGTG GAGAGGCATG CTCATTGCTC TTAGGCATTT 840
CAGCGTTCCC TCATGCTCAG AGCCGCAGAT TATTACCCCT GCTTTAGAGA TAAGAAAGGA 900
AAGGCTGCGG CACTGAAGGA TTTGGCTCTG CAGCGAAGAA GCGACCGAGC TCAGATTCTG 960
TGGCTTTGTG GTGGTGGTGA ACAAGCATCA TCACTCAGGT CTGTCTGCTT CAAGAAGTGA 1020
GAAAGGAGAC AGACCCATGG CCTAGCAGCT GCCCTCTGAG CCCATTGCAG TGTTCCTTAG 1080
GAGGCCACAC TGACTGTGGG CTGTGGCACC TGCCCCAGGC TGGTGACTGC ACAAGGGGCA 1140
GCTTCCTGGT CTCATCCAGC CCAGGGAAAC TCTCTTCCTC CTCAGAACCC AGTGAAGTCA 1200
CACGTACAGA GGCGTCTTCA GAGCAGCAGT GCTTAACCCA GAAGCTAGCA GTCTCCTGGT 1260
GACGATTGAG GCCTTGTTCT CCCTCCATCC CCCGCCCCGC CCCACCCCAG AGCTGCTGCT 1320
TCACCCTCAG GTTGGGAGGG GAGGGCACCC AGACCTGCAG CCAAGGACAG AGGGGCTAGA 1380
ATGAGGGTCC CAGACTCCTT GGGAAAGCTA CGGGCAGCTG GGCCCCTTGC AGCAGCCCCA 1440
GCTGTGGCTG CAAAGGGGAG AAGTGGCCCA GGTTCCTGCT GGAGAGCAGA GCCCAGGGGC 1500
ACCGGGAAGT GAGTCCCAGG AAGCAAGCCC AGAACACACA GCACACTTCT TAGCGGCTAG 1560
CCACCCTTCA GGCTATGCCT TCCAACTTCT CAAAGGCACA ATGACTTTAA AGATAAGTGC 1620
ATTCCATCTG GAGGCAAGAA CGCTCCCCAG CCCTCAGGGC CCCACACAGC AGCACAAGCT 1680
CGGCCATGTA CATGCAGCAA GCACCTCCAG TGTGAGATGA CGCCCACACA CGCTCACACA 1740
CACCCTCCCT GGCAGAGCCA CCTGTTCATG GCCCTCCTGG GCACAGTAGG AAAGTGGAGG 1800
AACCACGAAG AAGCCACAGA GACAAGCAAG AGGCAGAGGG AGGCCCGGGG AGAGCCCATA 1860
ATGAGGAAGG AGCCCGAAAG AAAACCAGAG ATGGGGAAAC CAAGAGCGAG CCCAGGGTGG 1920
CCAGACGCAC CCCCAGCAGG AAGGGCCCAG CACCTCTGGG GGAATGGGGT CCTCCCCCTC 1980
AGCTCACACC CTCAGGGCTG CTCCGAAAGG GGGAGCTGAG CCAGGCCTCA GCCCCCTTCC 2040
CTAGCTCCTC TGTGCCCCCA TACCTGGGGC CCCCATGTCC CCTGGGCTGG ATATGAGGTG 2100
GTGGCAGGAG GGGCTGGCTC TAGGGACAGG CATCTGTCAA CCTGCCCTCC CTCGAGGGAG 2160
ATGCTGCCAG CTCAGCTCTC ACTTCAGAGG GGACTCCCTC CCCATCAAAT TCCTTCCCTA 2220
TGGAGCCCAG TTGAGGCCCC CACATGTGCC CCTCTAGGTA AGCTCCACAA AGCTCACAGT 2280
GCAAAGCATG ACCACCAGGG AATCTCTCCT CCAAGGACTC ACCTTGGGGG ACACATCACC 2340
CTTGAACCCC CTCCCGTTGG GTTCATATCC CTAGGCCACC CTGAGGTGAT GACCGTTGGT 2400
CCTATTTTAC AGATGAAGAA ATCGAGGGTC AGGGCGGTCA CTCAGCTAAT GAGCTCTAGA 2460
GCCAGGATGC CACACCTGAT CAGTTCCAAA GCCCAGACTC AACTTTTGAC TCCCAAACTG 2520
GGGCACACAG ACACTGGGGG GAGCGGGCGT GTGTCTGGAG CTTGCTGAAG AAGATTCACA 2580
CTCCATCTTG CTTTGATCCA AAGATCGAAC TGGTAAAGAA AACACTTTTG TGACATAACC 2640
AACATAGACA 2650
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