| Tag | Content |
|---|
EnhancerAtlas ID | HS104-00433 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:12243860-12246730 |
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: 2 | Chromosome | Start | End |
| chr1 | 12243884 | 12246504 | | chr1 | 12245348 | 12245387 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I012182 | chr1 | 12242459 | 12247879 |
|
Enhancer Sequence | AGCTATCTAT CTATTCTATC TACCTATCTA TCTATCTATC TATCTATCTA CCTACCTACC 60
TACCTACATA TCTATCCATC CTCTCCGATT CCCTCACCAC TGGGTCTCAG ATTCCCTGCC 120
TGTTAAATAA ATGGTCAGTT AACCCTCAAC AGTGATTTTC AATTTTTCAC TTGAGGCCCC 180
CATATTTTGG AAGATTGTAG TTTGCTGAAC ACGCTGACTG AATCAAGTAC TATCCAACTT 240
ATTTCCTCAT TTTAACATGT CAAAGATCCC CTGTGGGGTG AGTGGGGTGT GAATTGGAGC 300
CTCCCCAATC CAAGGCACAG GAACTGGAAG CTTCTGTAGC CCTGCATTTC CTAGAGAATG 360
CTTGCCATGT TTTGGGGACC TCCTGGGGGG CCCCTGTACT GACCAGAGGC CGGCTCCCAG 420
GGCTGTGGTT TGGGCCCAGC CCCCTGCTCC TGGGGACTGC TGCTGTGGAG GGAGTGACCT 480
TTTGTTCTGC TTTGCCAAGG GGCTTTCTGT TCCTCATTGT TTAGCCATGA CAAGGCTGTG 540
GATTTTTTTT TTTTTTTCTG TCCAAGAGAA TAAACAGGCC TGAGATTGCT CAAGGGAGCC 600
GACCCCCTCT GCCAGCTACT GGGGGCTGGA GGCTCACAGA GCCAGGGAGG AAGTCCTACC 660
CCCTCTGCCG GCTACCGGGG GGGCTGGAGC CACACAGAGC CAGGGAGGAA GTCCAGGGAC 720
GGTCACTCAC AGCAAAGCCT CAGACAAGAG AGGAACCTGG AGGGGAGGAG GTGGGAGGCC 780
ACCACTCAGC CGGCCTGGGG GCCATGGGAG TCCAGCTGCC TGCCGTTAGT GGCCAGGAGC 840
CCTCGTCCAT TGCGGCTCTT GAGAGCCCAA ACTTGGCCAC GGCAGGGCTC TTTCCCATCA 900
GGCCCTTTGA GCCCTGATGG GAAACCCTTC CCCAGCCAGG GTGGGATTTC TTGCTGCCGC 960
CTGGAGCCGC CCTGGCCCTG TGGTTCTCAG GCCCTGGAGG AGTGAGGGGC TCCCCTGGTT 1020
ACCCCAAGGG CACTCGTGGG GATGAAGCCC GCGGGATGCA GGATTCCCAC GAGACCTGTG 1080
CTGGCCACTG TGCGGGGTGG GGGGCTGCCA GGGAAGAGGT GCAGCCCCTG CCTGCCTCAG 1140
GGATGCGATC TGAGGGAAGA GGCAGCTGTG TCTGGGAGGC CGTTCGGTCG GAGGGGGATA 1200
GGCACAGCCC CTGCCCTTGG GGAAGCGCCC AGCAGCAGCC TTCAGGGAAG GCAGTTTGGG 1260
GGTTTGCCGA GGGCCAGGAA GACCCTCTGC CGCAGTTAGT ATTCGATGGA ATGGCTTGTG 1320
CAGAGGGAGC TGCAGAAGCT GCCATTTCTC TGGGTTAGGG GCTCCCACAG CCTTTGGATG 1380
CCGGGTCTCG GCCATGAGCC CCCTCCGCCA CCCCTCCCCC AGGTCACCTT GCTCAATCCA 1440
GGAGGCCGGA TGATCAGAGT GTGTTCTGCA AAGGAGCGTG AGAATCACTG GGGAGATTTC 1500
CTTTTTCTTT TTCTTTCTCT TTTTTTAATG GTACAGCTTC CTGGGCCCAC CCCTGAGATT 1560
CTGCACTTGT TTGGGGAGTG GGTGTTGGCT TCATGACAGG CACCCCTGGG TGCTTTGGAC 1620
ACAGGCAGTG AGCTCCCCCC ACACTGTGTG AACCCCTGAG AAGGCTTCTC CTTTTGTCTA 1680
GGGTGCCTGG GAGTCTGCTC CAGCAGCAAA CCGGGGAGGG GAGGGGTACT GGGACCGAGT 1740
GTGTGTGGCA GCACCGTGTC CAGGCAAACT GAGGCTCCAG ACGGGGGTTA CTTCTTCAGA 1800
CCCTGTTATG CAGCATGGTT CCCACTGCCC GTGCCCAGAA TTCACCATAG CTGATGGGCC 1860
TGGGGTGGGC CTCCGGGGCA GGCCAGGGTG GAAAGTGCAT CTGTGTTTGA GCTTTGCGGC 1920
CCTGGCGCTG GAGTTAGATC CCTACAGGAA AGGACATTGT AACCCAGCCC GTGGTTGAGA 1980
CTAGCAGCTG CTGAGCACCT ACGCCCTGCT AGGCTGTGGG GCAACAGCAA AGGGTAACCC 2040
CCAGCCTGCA GCCTCAGGGG GGCTTCCCAT CTAGCGAGGG GCCCAGGGAG GCCATGAGGA 2100
GAGCCATGAG GGAGGAAGGT GGGGACTCTG GGCCTGAGTG ACTCCTTCAG GGTGGGGTGC 2160
GGGCAGGGAG CCTTCAGGAG GGAGGGTACT GCCTGAGCAG GGCTCTTAAG GGACACGTGG 2220
AATTTGTTAC AGGAAGCACC AGGCCATTCC AGGCATAGAA ATCAGCTGGG GTGCAAAGGC 2280
CTGGGGGTCA GAAGAGTGGC AGATTGCTCC ATGGCAGGAA GCCCCAGCTC CTCTGGGTCG 2340
TTCCCGCTGA GGGATTCCAG CTGTTGGCAC CGAGGGGTGC AGCCAGGGCA GGGTGGTGCT 2400
GCCTGCCAGG CTGAGGTGGG AGACAGCTGG GTTTCTAGCC CTGCTTGTCA CTCGCTATAG 2460
GTGCAGCCAA ACGCTCAGCA GGCCCAAACT CTGGGCAGTC CTGACTCCCA GGCAGTGCTG 2520
TGAGGAAGGG GAGGAGGAGG CACACTGAAC CCACCTGCTA CGTTGGCTGG TGGAAATTTG 2580
GCCAGGTCTG CACTGGCCCA GCGGTGCTGG GTGTCGTGAC TGGTGTCTGC TCTGACTGGC 2640
TTGCTGACAG CTGAAGTCCA GGATAGGTCC ATGGCCACGT TGTGCTGGTT TGTTAAATAT 2700
TTTTAGTATC TCCCCTGCTC CTATATGTTA GGTACTGGAG TCCAGAGAGG TTAAGGCACT 2760
TGCCTAAGGC CACACAGCCG CTAAGTGGTG GAGTGAGGAT TTGAAACCAG TTCTTTCTGA 2820
CTCCCTGTAT CCTTATCTAT GGAGAGGCCC CATGACTCGT TCACTAAAGG 2870
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