| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04282 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:206752380-206754730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:206754168-206754186 | CCTTCCTTCCCACCTTCA | - | 6.75 | | HSF1 | MA0486.2 | chr1:206753661-206753674 | GAAGCTTCTAGAA | - | 6.28 | | HSF1 | MA0486.2 | chr1:206753666-206753679 | TTCTAGAATTTTC | + | 6.71 |
|
| | Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
| SE_09327 | chr1:206745188-206758382 | CD14 | | SE_10603 | chr1:206747310-206756416 | CD19_Primary | | SE_11004 | chr1:206727079-206757887 | CD20 | | SE_11917 | chr1:206750311-206757762 | CD3 | | SE_14503 | chr1:206746009-206758997 | CD4_Memory_Primary_7pool | | SE_16490 | chr1:206750757-206757114 | CD4_Naive_Primary_8pool | | SE_16959 | chr1:206748089-206757504 | CD4p_CD225int_CD127p_Tmem | | SE_17411 | chr1:206724289-206760065 | CD4p_CD25-_CD45RAp_Naive | | SE_17843 | chr1:206723887-206758306 | CD4p_CD25-_CD45ROp_Memory | | SE_18269 | chr1:206723684-206769868 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19128 | chr1:206746389-206766399 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20034 | chr1:206746357-206757932 | CD56 | | SE_20823 | chr1:206746904-206757454 | CD8_Memory_7pool | | SE_22080 | chr1:206746077-206757652 | CD8_Naive_8pool | | SE_22390 | chr1:206744356-206757869 | CD8_primiary | | SE_25703 | chr1:206752909-206754508 | DND41 | | SE_27304 | chr1:206752644-206753579 | Esophagus | | SE_27304 | chr1:206753679-206754504 | Esophagus | | SE_31229 | chr1:206751813-206754781 | Fetal_Thymus | | SE_39708 | chr1:206752855-206753614 | Jurkat | | SE_39708 | chr1:206753678-206754514 | Jurkat | | SE_50667 | chr1:206747343-206754765 | Sigmoid_Colon | | SE_53261 | chr1:206746644-206756568 | Small_Intestine | | SE_53552 | chr1:206746429-206757806 | Spleen | | SE_55221 | chr1:206751935-206752738 | Thymus | | SE_55221 | chr1:206752840-206754343 | Thymus | | SE_59167 | chr1:206727342-206757447 | Ly3 | | SE_62534 | chr1:206724532-206763666 | Tonsil | | SE_65624 | chr1:206751492-206752726 | Pancreatic_islets | | SE_65624 | chr1:206752745-206755870 | Pancreatic_islets | | SE_66615 | chr1:206752855-206753614 | Jurkat | | SE_66615 | chr1:206753678-206754514 | Jurkat |
|
| | 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 |
| GH01I206573 | chr1 | 206746529 | 206757654 |
|
Enhancer Sequence | ACCCCTAGCA CCCAGCCTCT TTACATGGCT GTTCCCCAAT CACCTCCAGA GCTAAAAGAA 60
GACATTGCCC TTTTCCACCG CATAGGACAT GTGAGCACAA ACCTGTTTTT CACCAGTGCC 120
CTGGACATGC CAAGTGCATT GGGAACAGCT CAGCCATCTG CCACCAATGC CAGGGGCTTA 180
ATCGGAATAG ATGAATTCCA TGCCAGATGC ACTGAGATGT GTGAGCCCCC AGGAGAGACA 240
CCTCACATGC CAATGTCTAT ATTTGTTAAA TCATAACAGA GTTCCCTATT CTGTCTCTAT 300
CTTGGGCCAC CCCAAGAGGC AAAACTGTCT GCTTGGTTTC TCGCTTTGTA CCCGTGGACA 360
GATCCTTAAG AATCTGGCAG GTGAATAGGA ATCAGAGTCT TTGTCTTATC CTCTGAAGAT 420
TGCTATAGTA TCGATCTCGC TCTCATGGCA GATAGTGCCT GTTAGGTAAA CCTTTGGGGT 480
GTTTGTGTGT TTCTTGGCAC CAAGTGTTAA TTCAGCAGCT GGATGAAGAC CCTTGAGGTC 540
TGGAATTGTT GTGAGGGGTC TGTCTATTTC AGTTCTTTTC GAATGTTGCT GCGAATTAAA 600
ATCAACTAGG AGATTTTTAA AATTCCCATG CCCAGACTGC ACCCCAGACC AATTAAATCA 660
GAATCTCCAG GGATGAAGCC CAGGCAGCTA AGTTTCTAAA GATCCCCCAG ATGATTGCAC 720
TGTGCAGACA AGTTTAAGAA CCACTGGTCT GGATTATACG CCATCTCTTG GGTGGAAAAA 780
GGATCCGTGA GCCCTCGTGG CTGTGGCTGG CTGGCCTAAT TCAGGAGGTG ATTCATTTGG 840
TCCATGGGTC ACATCTTGTC TGCCAGATAT TTTTGTGGGC AGCAGCCATC CCAGACCTGG 900
GTGCTGGCAT TCCATGGCTG TGACATTCGT AGTGTTGGCT ACACACGGGG CTCCTGGCAC 960
TCCCAGACAG GGCTTCCCAT CACCAGCCAG AGGGCCAGGC CTCAGAATGG TGAGGTCAGG 1020
GCTGCTGTCT TTTGAGTCAG CCCTGGAAGG CAGAGGTGCC TGTGGCCACT TGCGTCACTT 1080
CCCCGCGTTT GTGGTGGGAA GGGGAGAGAT AGATGGGTCT ATCTGCTGAA GAAAGGGGAA 1140
CAGGAAGAAG AAACCCTAGG CTAAGGCAGC TTTGCTTCTC ACTGTATTCA AAATCAAGCC 1200
TTTGAAAGCC ACAGCACAGC TGCCTTTTCT TACGGGGAAA TGGCTCTAGC TTGATTGGAA 1260
ACTATGAGAG GAGATCTTTC CGAAGCTTCT AGAATTTTCT TTCCATTACT TATTTTTTAT 1320
AGACAAGTAT GAGAAAGCTA TTACCTCCTG AGGAGCAATA GCCTACATGC GTCAGAGACA 1380
GAGTGAGTGT ATAATAGTAA CCAGACAACG GGGTCTTTCT AATTAGAAGC TCCCAGCGGG 1440
AAGGTATAGG GGTAGGGCCA GGGTCAGGCA CATCTGGTCC CATAGACATG TGCTCAGCTG 1500
GCAAGGACTG AGGATGGGGA GCTCTGGGAG CTACCCAAGG GAAGGGATGA GGAAAATGAG 1560
AGGCTTCACT GTGAGAGTCC CCGGGTTAAT GGACTGACAG TGAATGAAGA GAGTCTGTGA 1620
GGCTCACACT ACTTGCTACT CACCTCCGGC AAGTGGGAGA TGGCCAGAGC TGCTTGCCCT 1680
TGGGTGGTCT GCAACAGAAT CAAGGTTCAG TTCCAGAGAC CTGGGAAGGC ACACAGGAGA 1740
AGGCTGGGCC CTGCATCCTG GTGGCTGCAT CTCACTTGAG TTAGAAGTCC TTCCTTCCCA 1800
CCTTCACAGG TGACATGGTG CCTCTGGGGC CTGACCCGCT GCTTAGACTC ATCTTAGATG 1860
AACATTTCAC AGATCAGGTA ACTTACAGGC TTTGGTTTAA CAGCTGCTCA TCCCAGCCCC 1920
GCAGCACAGA GTTTCAGTGA TCATTATGGG TGTGGCAGGC CGGCCCCTTC AGCAAAAGAT 1980
GCCGTCCCAT GGTGGCTACA TGGTGAATTG AGAAGAGCAT GGGCCTTAGA TGGATTTGAT 2040
TCCAGTTCCT ACTTAGCTTC TTACTAGCAG GGGACCACAG GCATGTTTCT TAAACTCAGC 2100
CTCAGTTTTG TTATCTGTGA AATAAGAATG ACATACATAG TATGTAAGAG AAGGTATGTG 2160
AAAGTACCCA GCACAGGCTG TTATTAATAG GTCAGGACCC CTTGGGGAGA GTACAGCGGG 2220
AGCAGACAGG CCAGGGAACG ATGCCACGAT GGAAAGAGGA TGTCAGAAGC TGGGTGCGGT 2280
GGCTCACACC TGTAATGCCA GCACTTTGGG AGGCCAAGGC GGATGGATCA TTTGAGGTCA 2340
GGAGTTCGAC 2350
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