| Tag | Content |
|---|
EnhancerAtlas ID | HS187-02729 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr10:3916310-3919220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr10:3917526-3917547 | CTGCTTTTTCACTTTCCTTTT | + | 6.19 | | Nr2f6(var.2) | MA0728.1 | chr10:3917098-3917113 | TGAACTCCTGACCTC | - | 6.22 | | Pou2f3 | MA0627.1 | chr10:3917620-3917636 | TGGTATGCAAATACAA | + | 6.23 | | Sox6 | MA0515.1 | chr10:3918632-3918642 | AAAACAATGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_00402 | chr10:3915033-3916720 | Adipose_Nuclei | | SE_00402 | chr10:3916891-3918409 | Adipose_Nuclei | | SE_11993 | chr10:3914330-3920413 | CD3 | | SE_12963 | chr10:3914381-3918104 | CD34_Primary_RO01480 | | SE_13708 | chr10:3913755-3918567 | CD34_Primary_RO01536 | | SE_14266 | chr10:3914210-3918013 | CD34_Primary_RO01549 | | SE_14266 | chr10:3918860-3919875 | CD34_Primary_RO01549 | | SE_14734 | chr10:3913700-3920543 | CD4_Memory_Primary_7pool | | SE_16571 | chr10:3915092-3920110 | CD4_Naive_Primary_8pool | | SE_17072 | chr10:3914206-3920417 | CD4p_CD225int_CD127p_Tmem | | SE_17970 | chr10:3913366-3920978 | CD4p_CD25-_CD45ROp_Memory | | SE_18564 | chr10:3913804-3920617 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19317 | chr10:3913870-3920544 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_21176 | chr10:3914759-3920435 | CD8_Memory_7pool | | SE_22812 | chr10:3914892-3920406 | CD8_primiary | | SE_36602 | chr10:3916048-3916883 | HMEC | | SE_38245 | chr10:3918683-3920350 | HUVEC | | SE_46298 | chr10:3918669-3920257 | Osteoblasts | | SE_47115 | chr10:3915930-3916787 | Panc1 | | SE_47115 | chr10:3916952-3918159 | Panc1 | | SE_47115 | chr10:3918398-3923064 | Panc1 | | SE_53169 | chr10:3916146-3916808 | Small_Intestine | | SE_53169 | chr10:3916860-3919399 | Small_Intestine | | SE_64554 | chr10:3916133-3917028 | NHEK |
|
| | 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 |
| GH10I003871 | chr10 | 3913478 | 3920369 |
|
Enhancer Sequence | AGGCTTTTGC ATAGTAAACA TGATACCAAT TTTATTCACA AGTTATAAAA CACTGTAATT 60
TAATAAGAGG ATATTCCAAT ACATGAGACA GACGCAGGCA GAGGCTCACT GTCTTCAGAT 120
TCAAATGACT ACTTTTCCGT TGGCTGGATG ATTTAGCCTC CCCAAACCTC CACAGTCGTT 180
TATAACCTAC CCACGGTGAT CATTACCTTT GCCATTTTTG CATTTTAAGT CATTTCTACC 240
AGTCTTGTCT TTTATTTCAT AGCCCCAAAG GAACAGCTCT GAAATAGATT TCAAGGAATC 300
TTTACTACTT CCTATTTTGC TCCAACTGAA ACAAAAGAGA AAAGTAACTT TATTAGATTT 360
TTGTTTTTTG CCTTTAAATT TGTTTATCAT TATCTTTATT TTTATTTTAT TTTATTTTTT 420
GAGACAGAGT TTCCTTCTTG TTGCCCAGGC TGGAGTGCAG TGGCATGATC TTGGCTCACT 480
GTAACCTCTG CTTCCTGGGT TCAAGTGATG CTCCTGCCTC AGTCTCAGAG TAGCTGGGAT 540
TACAGGCATG CACCACCACG CTGGCTAATT TTTTTTTTTT GCTTTTGAGA CAGAGTTTCA 600
CTCTTGTTGC CCAGGCTAGA GTGCAATGGC ACGATGTTGG CTCACTGCAA CCTCCACCTT 660
CCTGGTTCAA GTGATTCTCC TGACTCACCC TCCAGAATAT CTGGGATAAC AGGCATGCAC 720
TGCCATGCCC GGCTAATTTC TGTATTTTTA GTAGAGACAG GGTTTCTCTA TGTTGGTGAG 780
GCTGGTCTTG AACTCCTGAC CTCAAGTAAT CCTCCTGCCT TGGCATCCCA AAGTGCTGGG 840
ATTGCAAGCA TGAGACACCG CACCTGGCCC ATCATTAACT TTAATTTCTT CTCTGAGAAG 900
CAAATCTTGT GGACTCCTTT AGAAACGGAA CTGAGCCTTA CCTCCAGCTC ACAACCCACG 960
TCCGGTAAAA TAGTTTTGTG TAATTGATTA AATTTGACTC CTAGGGGTGA GTTTTCAGCT 1020
CACATAGGGA AAGGAGGGAA GCAGTGCCCA TCACAGCGGA AATGTGGACA CTGCTTTTAT 1080
TTGAGGGAAG GAAGGGGAGC TGTCTGCACA ATCCCATGAC ATTGTGGTTT TCTGCCAGAT 1140
GCTTGGAGAC AATGTACTCC AGTGCGCACA CCTGCTTCTT TACACTCTGA CCCATTTAAC 1200
AAGCTATGTC AGAAGCCTGC TTTTTCACTT TCCTTTTGAG TATGTCCTCC TTTAAGGACA 1260
TATTTATTAA TAAATGGGGT TTCCCTCCTA AATTTGGCAC TAAAAGGGAT TGGTATGCAA 1320
ATACAACATA GTACTTGGCA AATGTAAAAA AAAAAATTGT ACTGCTTTGG GGGAAGGGTC 1380
AACAATGAAC TAAAGGTGGT GACAAATGTA AACTCAGGAT GCCTTAGAGT GTGGGTGTTA 1440
GGCAGTCAGA CAGGTAAGTG TGAACCCCAG CTCAGACATT TAGTAGCTGT GTGAATTGGG 1500
GCCCTGACTA GACTCCCCTG AGCCTTGGTT TCCTCATCTG TAACATAAGG AAAATACCAC 1560
CTACTGTGCC GAGTTGTTGA AAAATCTGAG ATGTTAGAAG TCACCTGCAT TTTGAAACTT 1620
GAAGTGATGC ATTTTTTCAT CATTTCTGAT TTGTCCCATG CCTACAGGAA GAGAGTGTGC 1680
CACCTTTGAT CACAGAGTAC TTTCATTTTG CTGTATCTGT GGTTACATTT TATTGATGTG 1740
CATGGCCATT GTTACATTTT ACTGATTTTC CTTCCTTATC AATTGGATCT CGAGGTTCAG 1800
AAAGTGCCAG ATTCCTCTGT ATCTGCACGA AGATGCATCT ATGGAAGTGC ATCTCCCCTG 1860
TCATGGAGAT CCTCCAGCTC CTCCAGCTCC TCCAGCTCCT CCAGCTCCTC CAGCTTCTGC 1920
CCATCACCTT TCCATCTCCT GACCTGACTC CTGGCTGAGG TAGTGTTTTC CAATCAAGAC 1980
AAAAGCTCCT GAGAGCTTCC ATCAGTGTGG TTCCCGGAAT AGTCAGCTGA CTTGTAAATG 2040
GAAAGCCCTA GAGAAAAACA AGTCCTTCTC TGATCTCAAT CTTAGCAGTA TCACCTAAGC 2100
CAGTGTTTCC AACCTTTCAT GCACACAGTG ATCACCCATG GGCCTTGTTG AAAGGCAGAT 2160
TTTGGCTCAG CAGGCCTGGG TGGGAGTTGA GCCTCTGCCT GGCTGATGAG CTCTCAGGGG 2220
ATGACCAAGT ACCTGGTCTA GGAGCCTCAC CTCCAACGGG AAACTCTCCA AAACACAGAT 2280
TTTTATCAAA TTTGTTCAAG CCCTAATTAG AGGCCACCAC CCAAAACAAT GGGTCCCCAG 2340
ATGACTTTAG CCTGGGCATA TTTGGGGTTT TTCTTCTAGT ATAAGATTCA GGCTATCCAG 2400
CCTTTTTTTT TTTTTTTTTT TTTTTGAGAT AGAGTCTCAC TCTGTCTCCC ACGCTGGAGT 2460
GCAGTGATGT CATCTCGGCT CACTGCAACC TCTGCCTCCT GGATTCAGGC GATTCTCCTG 2520
CCTCAGCCTC CAAGTAGCTG GGATTACAGG CACCCACCAC TGCGGCTGGC TAATTATTGT 2580
ATTTTCAGTG GAGACAGGGT TTCACTATGT GGGCCAGGCT GGTCTCAAAC TCCTGACCTT 2640
AGGTGATCCT CTCATCTCAG TCTCCCAAAG TCTGGGATTA CAGATGTGAG CCACCCTGCC 2700
AGGTCGGTCC AGTCTTAGTT GAATTTGGCT TCCTTGTACG ATAAAGAGAC TGGGCTGACT 2760
GGAATCTCTC GGGTCCTTTT CAATAAGCAA ATGCAGCATA CTTTCTTCTT ACAGAGGTGG 2820
GACAGATCAG GGAAGATGCA AAATTCATCT GTTCACATTG TCATTACCAA ATTCCTTTCA 2880
GCTTACCGAA ATCTTCTCTG AGCCTTAGGA 2910
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