Tag | Content |
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EnhancerAtlas ID | HS180-04726 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:226884120-226885590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr1:226885200-226885215 | GGGTGTCAGAGGTCA | + | 6.34 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00103 | chr1:226883705-226886259 | Adipose_Nuclei | SE_03869 | chr1:226882978-226886945 | Brain_Anterior_Caudate | SE_04801 | chr1:226882860-226887506 | Brain_Cingulate_Gyrus | SE_05781 | chr1:226882582-226887714 | Brain_Hippocampus_Middle | SE_06710 | chr1:226882929-226887612 | Brain_Hippocampus_Middle_150 | SE_07746 | chr1:226861943-226887535 | Brain_Inferior_Temporal_Lobe | SE_10211 | chr1:226883113-226887633 | CD19_Primary | SE_10887 | chr1:226873819-226893407 | CD20 | SE_11833 | chr1:226884870-226885986 | CD3 | SE_14432 | chr1:226885121-226886000 | CD4_Memory_Primary_7pool | SE_15808 | chr1:226885089-226885992 | CD4_Naive_Primary_7pool | SE_17296 | chr1:226856971-226887803 | CD4p_CD25-_CD45RAp_Naive | SE_17765 | chr1:226858457-226887760 | CD4p_CD25-_CD45ROp_Memory | SE_18263 | chr1:226857891-226887822 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19160 | chr1:226883999-226886167 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20012 | chr1:226883215-226887069 | CD56 | SE_21910 | chr1:226883715-226886974 | CD8_Naive_8pool | SE_22315 | chr1:226882979-226887479 | CD8_primiary | SE_25774 | chr1:226883181-226887670 | Duodenum_Smooth_Muscle | SE_26570 | chr1:226883956-226887261 | Esophagus | SE_29606 | chr1:226884506-226885789 | Fetal_Muscle | SE_40782 | chr1:226884801-226885783 | Left_Ventricle | SE_48218 | chr1:226884845-226887424 | Psoas_Muscle | SE_50140 | chr1:226884168-226886179 | Sigmoid_Colon | SE_51367 | chr1:226884676-226887386 | Skeletal_Muscle | SE_52562 | chr1:226884081-226886148 | Small_Intestine | SE_53341 | chr1:226884203-226886402 | Spleen | SE_54498 | chr1:226882945-226887509 | Stomach_Smooth_Muscle | SE_58303 | chr1:226819953-226937809 | Ly1 | SE_59629 | chr1:226819233-226928465 | Ly4 | SE_60416 | chr1:226819368-226929640 | DHL6 | SE_61009 | chr1:226812849-226900772 | HBL1 | SE_62233 | chr1:226813614-226929647 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I226695 | chr1 | 226883341 | 226887082 |
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Enhancer Sequence | CCCTGGCACG TAGATAGCAA CTTATTTTAC TATCTTGGAC ACCGGCTTCC ACTTCCGACA 60 AGGCCAAAAC TTAGAGACGA AATGGCACAT GCCCGGCCCC TGTATTTTCT ACTGTTTTCT 120 GAGAACATAA TTTCTAGTTG GAGTATTAAT TACTAGCTTG GAGCATTACT AGCTGCTGCT 180 ATTTCTCAGG GTCCCCTTGG AGACCAAGCA ACCGCTAAGA TGGCTGGCTT TCTCCATAGA 240 ACTCACAGCT AGCACCAGCA ATGAGGAAAT ACGCACACGC GCACACACAC ACACGCAGTC 300 TTTACATCTG GTTAGGGCTC CAAGTATTTC CTAAGTGTCT CATCACACTT ACTAAGGCCT 360 GAGAATCTCA GAGCTGAGAC ACTGCAGAGG TGATGTAGCC CAAGCCATCC CCTGAGGCCT 420 GAGTGTCCTC TGCAGCACCC GACTAGGGGC CGGGGGGTTA GCACAACCTG TCCCCATTCC 480 CAGGAAAAAA CCCAGCACAC AGCTCACACT CAATGATGTC AGCTTCCTAC AGGAAGGACA 540 GGTACAGCAT CACTAATTAA AAAGAGGTCA CAACCACGAA GTTCATTCAT CCAGGCCTCT 600 TGGGAACAAA TCATATCAAC AACCACCAAA CAAATGGATT CATGTTAATT TGGAGGTATT 660 CTTATCTGAG AGCAATAGAA TATAGTTCAC CAAAGCAGAA ACCTGGGCAA GCGTCAACTA 720 AATGTTGGTG GGTCCAGGAA GAAATCCACT GATTCAGGCT AGGTGCCTGT CACAACTTGG 780 TTAGCCTTTC TGAACCTGTT TCCTTGTCTG AAAGATGAAA GTAGCAATAG TTGCTGTGAG 840 GCGTGATTAA GGCATGATGC ATTCAGAGGC ATAGTACAGT GTCTGGCAAA GATTCAAGAA 900 ACTTTAGACT CTTTCCCCTT TCTGCACCAA TAAGCAAATC TGAAAAGATC ATGAATACAC 960 AGTGCTGCAA AATGAGAAAC AGAATTTCCC CCTTTAGACA AGAGAGCACT GTGATGCAGA 1020 CACAGCCCTG GCATCAGCAA GGAAGGCCCT GGTTCCCCTT CTCATCATCC CTGGAGAGAT 1080 GGGTGTCAGA GGTCAGGTGA GGGAATCTCT TTGTGCGTGA TTCTCCAACT CTGCAAACAA 1140 TAGCTGGCCA TTTCTTCTGA GGAATAAGCT GAAATCAAAC ATACCTGATA GGCGAACTGG 1200 GCTTGATGCA GTCCCAAGCA CTCTGCTGAG CACTGAAGCC ACTTTTCCTC ACCACAACTA 1260 TGGGAGCTAG AGAAGGGAGG CGATTAGTGG TGAAGACAGT GGGGACCTGC CCCAGGTGGC 1320 ATTAGTGAAA TAGACAATTC TCTAGGGTCC TCTGCACCAA CCCAGAACTC TCCACATAAG 1380 AGCTGCCCTA GGAACACCAC AGTTCTGTGG CCTGCCCTGG CAGATGTGCC CTCACATCTG 1440 GGTGATAAGG GGTCCCCAAG AGGAGCCAAA 1470
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