| Tag | Content |
|---|
EnhancerAtlas ID | HS047-00266 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:12243850-12246770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:12245361-12245382 | TTTTTCTTTTTCTTTCTCTTT | + | 6.77 | | ZNF263 | MA0528.1 | chr1:12245259-12245280 | CCCCTCCGCCACCCCTCCCCC | - | 6.22 | | ZNF263 | MA0528.1 | chr1:12246380-12246401 | TGAGGAAGGGGAGGAGGAGGC | + | 6.78 | | Znf423 | MA0116.1 | chr1:12245459-12245474 | GCACCCCTGGGTGCT | - | 6.35 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00369 | chr1:12226565-12247198 | Adipose_Nuclei | | SE_01471 | chr1:12243922-12246504 | Adrenal_Gland | | SE_04546 | chr1:12243735-12246962 | Brain_Anterior_Caudate | | SE_06521 | chr1:12243738-12246994 | Brain_Hippocampus_Middle | | SE_09154 | chr1:12224797-12249846 | CD14 | | SE_10696 | chr1:12243928-12245111 | CD19_Primary | | SE_14553 | chr1:12243811-12245422 | CD4_Memory_Primary_7pool | | SE_14553 | chr1:12245589-12247318 | CD4_Memory_Primary_7pool | | SE_17827 | chr1:12231021-12246713 | CD4p_CD25-_CD45ROp_Memory | | SE_18389 | chr1:12226183-12250288 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19117 | chr1:12243746-12249924 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20048 | chr1:12243749-12245373 | CD56 | | SE_20873 | chr1:12243794-12244892 | CD8_Memory_7pool | | SE_22347 | chr1:12243335-12245917 | CD8_primiary | | SE_26251 | chr1:12243680-12246989 | Duodenum_Smooth_Muscle | | SE_27503 | chr1:12243903-12246642 | Esophagus | | SE_30788 | chr1:12243698-12246708 | Fetal_Muscle | | SE_32030 | chr1:12243891-12246634 | Gastric | | SE_38661 | chr1:12243533-12246545 | HUVEC | | SE_41498 | chr1:12243811-12247059 | Left_Ventricle | | SE_42336 | chr1:12243813-12247305 | Lung | | SE_48967 | chr1:12243799-12246749 | Right_Atrium | | SE_50250 | chr1:12243815-12247081 | Sigmoid_Colon | | SE_52522 | chr1:12243745-12249859 | Small_Intestine | | SE_53313 | chr1:12243756-12247385 | Spleen | | SE_55394 | chr1:12243888-12244461 | Thymus | | SE_55394 | chr1:12244622-12245112 | Thymus | | SE_61096 | chr1:12184746-12245090 | HBL1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 12243884 | 12246504 | | chr1 | 12243852 | 12244671 | | chr1 | 12245348 | 12245387 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I012182 | chr1 | 12242459 | 12247879 |
|
Enhancer Sequence | CTATCTATCT AGCTATCTAT CTATTCTATC TACCTATCTA TCTATCTATC TATCTATCTA 60
CCTACCTACC TACCTACATA TCTATCCATC CTCTCCGATT CCCTCACCAC TGGGTCTCAG 120
ATTCCCTGCC TGTTAAATAA ATGGTCAGTT AACCCTCAAC AGTGATTTTC AATTTTTCAC 180
TTGAGGCCCC CATATTTTGG AAGATTGTAG TTTGCTGAAC ACGCTGACTG AATCAAGTAC 240
TATCCAACTT ATTTCCTCAT TTTAACATGT CAAAGATCCC CTGTGGGGTG AGTGGGGTGT 300
GAATTGGAGC CTCCCCAATC CAAGGCACAG GAACTGGAAG CTTCTGTAGC CCTGCATTTC 360
CTAGAGAATG CTTGCCATGT TTTGGGGACC TCCTGGGGGG CCCCTGTACT GACCAGAGGC 420
CGGCTCCCAG GGCTGTGGTT TGGGCCCAGC CCCCTGCTCC TGGGGACTGC TGCTGTGGAG 480
GGAGTGACCT TTTGTTCTGC TTTGCCAAGG GGCTTTCTGT TCCTCATTGT TTAGCCATGA 540
CAAGGCTGTG GATTTTTTTT TTTTTTTCTG TCCAAGAGAA TAAACAGGCC TGAGATTGCT 600
CAAGGGAGCC GACCCCCTCT GCCAGCTACT GGGGGCTGGA GGCTCACAGA GCCAGGGAGG 660
AAGTCCTACC CCCTCTGCCG GCTACCGGGG GGGCTGGAGC CACACAGAGC CAGGGAGGAA 720
GTCCAGGGAC GGTCACTCAC AGCAAAGCCT CAGACAAGAG AGGAACCTGG AGGGGAGGAG 780
GTGGGAGGCC ACCACTCAGC CGGCCTGGGG GCCATGGGAG TCCAGCTGCC TGCCGTTAGT 840
GGCCAGGAGC CCTCGTCCAT TGCGGCTCTT GAGAGCCCAA ACTTGGCCAC GGCAGGGCTC 900
TTTCCCATCA GGCCCTTTGA GCCCTGATGG GAAACCCTTC CCCAGCCAGG GTGGGATTTC 960
TTGCTGCCGC CTGGAGCCGC CCTGGCCCTG TGGTTCTCAG GCCCTGGAGG AGTGAGGGGC 1020
TCCCCTGGTT ACCCCAAGGG CACTCGTGGG GATGAAGCCC GCGGGATGCA GGATTCCCAC 1080
GAGACCTGTG CTGGCCACTG TGCGGGGTGG GGGGCTGCCA GGGAAGAGGT GCAGCCCCTG 1140
CCTGCCTCAG GGATGCGATC TGAGGGAAGA GGCAGCTGTG TCTGGGAGGC CGTTCGGTCG 1200
GAGGGGGATA GGCACAGCCC CTGCCCTTGG GGAAGCGCCC AGCAGCAGCC TTCAGGGAAG 1260
GCAGTTTGGG GGTTTGCCGA GGGCCAGGAA GACCCTCTGC CGCAGTTAGT ATTCGATGGA 1320
ATGGCTTGTG CAGAGGGAGC TGCAGAAGCT GCCATTTCTC TGGGTTAGGG GCTCCCACAG 1380
CCTTTGGATG CCGGGTCTCG GCCATGAGCC CCCTCCGCCA CCCCTCCCCC AGGTCACCTT 1440
GCTCAATCCA GGAGGCCGGA TGATCAGAGT GTGTTCTGCA AAGGAGCGTG AGAATCACTG 1500
GGGAGATTTC CTTTTTCTTT TTCTTTCTCT TTTTTTAATG GTACAGCTTC CTGGGCCCAC 1560
CCCTGAGATT CTGCACTTGT TTGGGGAGTG GGTGTTGGCT TCATGACAGG CACCCCTGGG 1620
TGCTTTGGAC ACAGGCAGTG AGCTCCCCCC ACACTGTGTG AACCCCTGAG AAGGCTTCTC 1680
CTTTTGTCTA GGGTGCCTGG GAGTCTGCTC CAGCAGCAAA CCGGGGAGGG GAGGGGTACT 1740
GGGACCGAGT GTGTGTGGCA GCACCGTGTC CAGGCAAACT GAGGCTCCAG ACGGGGGTTA 1800
CTTCTTCAGA CCCTGTTATG CAGCATGGTT CCCACTGCCC GTGCCCAGAA TTCACCATAG 1860
CTGATGGGCC TGGGGTGGGC CTCCGGGGCA GGCCAGGGTG GAAAGTGCAT CTGTGTTTGA 1920
GCTTTGCGGC CCTGGCGCTG GAGTTAGATC CCTACAGGAA AGGACATTGT AACCCAGCCC 1980
GTGGTTGAGA CTAGCAGCTG CTGAGCACCT ACGCCCTGCT AGGCTGTGGG GCAACAGCAA 2040
AGGGTAACCC CCAGCCTGCA GCCTCAGGGG GGCTTCCCAT CTAGCGAGGG GCCCAGGGAG 2100
GCCATGAGGA GAGCCATGAG GGAGGAAGGT GGGGACTCTG GGCCTGAGTG ACTCCTTCAG 2160
GGTGGGGTGC GGGCAGGGAG CCTTCAGGAG GGAGGGTACT GCCTGAGCAG GGCTCTTAAG 2220
GGACACGTGG AATTTGTTAC AGGAAGCACC AGGCCATTCC AGGCATAGAA ATCAGCTGGG 2280
GTGCAAAGGC CTGGGGGTCA GAAGAGTGGC AGATTGCTCC ATGGCAGGAA GCCCCAGCTC 2340
CTCTGGGTCG TTCCCGCTGA GGGATTCCAG CTGTTGGCAC CGAGGGGTGC AGCCAGGGCA 2400
GGGTGGTGCT GCCTGCCAGG CTGAGGTGGG AGACAGCTGG GTTTCTAGCC CTGCTTGTCA 2460
CTCGCTATAG GTGCAGCCAA ACGCTCAGCA GGCCCAAACT CTGGGCAGTC CTGACTCCCA 2520
GGCAGTGCTG TGAGGAAGGG GAGGAGGAGG CACACTGAAC CCACCTGCTA CGTTGGCTGG 2580
TGGAAATTTG GCCAGGTCTG CACTGGCCCA GCGGTGCTGG GTGTCGTGAC TGGTGTCTGC 2640
TCTGACTGGC TTGCTGACAG CTGAAGTCCA GGATAGGTCC ATGGCCACGT TGTGCTGGTT 2700
TGTTAAATAT TTTTAGTATC TCCCCTGCTC CTATATGTTA GGTACTGGAG TCCAGAGAGG 2760
TTAAGGCACT TGCCTAAGGC CACACAGCCG CTAAGTGGTG GAGTGAGGAT TTGAAACCAG 2820
TTCTTTCTGA CTCCCTGTAT CCTTATCTAT GGAGAGGCCC CATGACTCGT TCACTAAAGG 2880
TTATGGATCT CGATCTTGTA CTGGCCACAT GACTGCAGCT 2920
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