EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-08289 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr10:3847420-3850230 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXC1MA0032.2chr10:3848865-3848876TAAGTAAATAT+6.14
IRF1MA0050.2chr10:3849593-3849614CACTGCTTTCACTTCCCATTT+6.21
RELAMA0107.1chr10:3848569-3848579GGGAATTTCC+6.02
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00402chr10:3845037-3857309Adipose_Nuclei
SE_11882chr10:3844923-3855094CD3
SE_13060chr10:3845435-3848784CD34_Primary_RO01480
SE_13486chr10:3844592-3849669CD34_Primary_RO01536
SE_14165chr10:3844524-3848919CD34_Primary_RO01549
SE_14454chr10:3844440-3855702CD4_Memory_Primary_7pool
SE_15590chr10:3845348-3850761CD4_Memory_Primary_8pool
SE_16065chr10:3845930-3848807CD4_Naive_Primary_7pool
SE_16065chr10:3848912-3850406CD4_Naive_Primary_7pool
SE_16325chr10:3844818-3854942CD4_Naive_Primary_8pool
SE_16945chr10:3845071-3854779CD4p_CD225int_CD127p_Tmem
SE_17898chr10:3842562-3855349CD4p_CD25-_CD45ROp_Memory
SE_18262chr10:3843866-3855308CD4p_CD25-_Il17-_PMAstim_Th
SE_19252chr10:3844144-3855295CD4p_CD25-_Il17p_PMAstim_Th17
SE_20116chr10:3844478-3854992CD56
SE_20771chr10:3844502-3855029CD8_Memory_7pool
SE_21756chr10:3845654-3850022CD8_Naive_7pool
SE_22443chr10:3844580-3856035CD8_primiary
SE_25500chr10:3843057-3856858DND41
SE_26256chr10:3844553-3854705Duodenum_Smooth_Muscle
SE_35818chr10:3845057-3856086HMEC
SE_37615chr10:3845967-3850357HSMMtube
SE_38247chr10:3845355-3854596HUVEC
SE_40296chr10:3847285-3849416K562
SE_41340chr10:3847447-3854927Left_Ventricle
SE_42946chr10:3847414-3854892Lung
SE_44151chr10:3844476-3852068NHDF-Ad
SE_44780chr10:3846400-3850379NHLF
SE_45602chr10:3844807-3850344Osteoblasts
SE_47115chr10:3844078-3857005Panc1
SE_50955chr10:3847406-3852855Sigmoid_Colon
SE_51836chr10:3846166-3851778Skeletal_Muscle_Myoblast
SE_52694chr10:3847404-3854725Small_Intestine
SE_55908chr10:3845063-3850948u87
SE_57501chr10:3847517-3848548VACO_503
SE_57501chr10:3848650-3850714VACO_503
SE_63160chr10:3844860-3855094Tonsil
SE_63583chr10:3846087-3854622HSMM
SE_64398chr10:3845568-3854714NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1038480373849536
Number: 1             
IDChromosomeStartEnd
GH10I003802chr1038445943855677
Enhancer Sequence
CTGTATTTTA CATGTTTCTC TGAAGAAAAT GTATTATTTA GAAAACAAAC AGTGTTGCCA 60
TGTGATAGGT TTTTTTTCAA ATGAGACAAC ACAACGGAAT AAAATATATG ATCTGTAGCT 120
GCTGAGGCTG AGTCAGTTCC TGTTTCAATA ACAAGAGTGT CATCTGCTAA ACTCTAACCA 180
GCACAATTTG TCACCGTGGA TGTGGCTTTA TTTGTACATG TTGCCAGAAA GTTCTTAGGG 240
AAAATTCACT CATAGTTTTC ATACCAAAAA AGAAACTTTT GGTGAGCAGT TCTGGCTCCG 300
GCTGTGGCCT TGTTTATTAT TTATGCTGTA ACCAATGCTT CCCTAATGGA AGGGTAATGC 360
TTGCCTAGCT ACATAAAATA ATGCCTCAGT TTTCTCTGGG GAATTAATAA TTTGCTCATG 420
TCACCCCAAA GCTCTCACAC GCTTGTGCGG TAGTTTTCCA AACAGTGAGC AGTGCGCCCC 480
AATGGCATGG CAGAGAGAAT TCCCAAGCTG AGAATCAGAA GACCTGCAGT TTTGTCTGGC 540
TTTGCTAAGT GACTTTTGGA TCTTGGACTT CTGTTTTCAC ATCTACAGAA TTATGCCATT 600
GAATAACATG TTCTCTATGC TTTCTTCTAG CGAAAAACTC TCTTAATTCT TTTTCTAGAA 660
TCATGAAATT GAGTTGGCAG TCTTTGCTTG GTCAGAGCCT GATGTTTCCT GAATTTAGAA 720
CTTGGTTCCC CCGAGACCCT CTGGACTAAT TTAAAATGAT TCATCCGCGT GAGTCATTGC 780
CCTGCTGCCT TCAGGACAAG ATGTCTATCT ATTGTCTTGC TGCTACCATT TTTTACAAAT 840
AACTCCAGCT CAGCAGCTGC AGACTCGAGA CCCTGCACCT GGTGACATCG GCCGGAAGAC 900
ATCAGCTGGC TCTCTGCAGA CACACCTGGA GGGAGGGTTT GGGAGGAAGG GGGCTGGGGC 960
CTCCGGTCTG ACCACCTCTG AAACACCATC CCAGGCTGTC TCTGAGGTTC ATGTGGTTTG 1020
GGTCAGATTC TCAGTAGAAT GAGAGGCATT TCAGGGACCT TCCAAGTCCT GAAAGAAGCC 1080
ACTGGGCAAA TAATTGGGTG TCACATTCCT TTTAGAGCCA GAAGGAAACA ACATCCTATC 1140
AGAAGGAAGG GGAATTTCCT GCCATGAAAA GGAATCTTAG AGCAAAACCG AGTCATGGTT 1200
TTGCCCGAAT TTTAAAATCC TGTTGCTTAT ATGGAAGCAT ATGGGTCCTA ACAATTTCTC 1260
TTTCAAAATC CTCATAGTGA ATGACATTAT GGCCATGTTT CTCCCTCAAG TGTGTCTTAA 1320
AAATGCATCT AGAGTCTAAC TATAAAGGCA TCATTCAGTT GTAATAATTA ACATCTTATT 1380
TGCATTCAGT ACAATTCTAA GTTCCACATA AGTGTCTAAT CTGGTGATGG GCGTTGTATG 1440
ATTGCTAAGT AAATATTTGC CGTTGGTTAT AAAGAATGAA TAAGATGGGC ACGGCCCTGT 1500
TTTCCTGTTG TCGTAGCCCA GGGTTGCCTT CTCTATAAAC TATGTGTGAC TGCAGCTGAA 1560
TCAGTGAAGC CATCACCACC GGCCTCATGC ATCACTGTCC TGTGGACCTG TGAGTAGTTC 1620
CAACACTCCC ATGTGGTCAG CCTGCTTTAC TTGAAACTCA GTTACATAAA CCTGTTGAAG 1680
ATAATGCTGC TATGTGATTG CTGACAACTT TCCAAATGCC CTGTTTGCTG CTCAAGCTGA 1740
TGTTCCCAAG GAGAGAGTTG CAAGTATTGG AGGAAGCACC ACCCTCAGGG AATGAGCTTG 1800
CAATCTGCTT CTCTGTGGCC CTGGGTCAGT CCCAATGTGA GCATGCCAAA GAGGACCCAG 1860
GCTGACGTTG GGGTTTCCAT CCGTTCAGAA TGACTTGATC CTTCCCTACC AATTAGAACT 1920
AATTAGGGTC TCTGGGTGCC ATGAAGATCA CGAGAAATGC AGAGTCTACT CCTGAATTGC 1980
TTTGTTTCAT CAAATGTCTG TGGCTAGATA TCAACTAGGG TTGCCATTTC CTGCTTCAGT 2040
TCAAATCAGA CCGATAATTG CGTTCTGCAG TTGTCTCCAG CTAGCTGGTC CTCCCTTCCA 2100
GGCCCTCTCT CTGCCAGTCT GCTCTGTGCT TCAGGAGAAT AATCCTCCTG CCATAGATTG 2160
ATGGATGCCT GCACACTGCT TTCACTTCCC ATTTTAAGAC CTCATCCCTC CAGGCAGCCT 2220
CCCTTGGTTT GGAATCTTGG CTGTGAATTG CCAAACCTCA AGCCCCCTGC AGACTTACTT 2280
AGCTCTGCGT CCCTATAACA TCCCATAGCT CCAGCCGTAT CCGTCTGCAT CCCAGCCCGC 2340
AGTGCGGTCA AGAGCTGTAA AGTCACTTCT CTCCTTCTGG CTGGTTGTTT ATGTGGACTG 2400
ACTGTCCTGC TGGCTGCCTT TGCTGATGAG AGTGTTGCCT TCCACAGAGA TCAGGCCACC 2460
TGGGAGAGCC ACTTCTGTCC ACCCATCCCT GAGGGGATGC TTCTCCGTCC CTTCTGCATG 2520
CCTCCTGCAC TCGGTGGCTG TGCTCTGGGA GAGTTACCCT GCGATCTACA CTTTCGGCTG 2580
CACCACCCTC TGCAGTGAAG AGTGTCTAAG GTTTCCCTAC TGCACAGAAC ACTCGAGATC 2640
CGTGGTGTGA CAGGAAGAGC TTTCCAGCTG CGTGGCCTTG GGCCGTCTTA CTCTCTGGGC 2700
CTCAGTTTCC TCATTGGTAG CATGGAGCAC TGAAAGCTAC GAACAGGAGC TGTGAGGGTG 2760
AATGGAGGAT TCATGCCAGA GCCTGGTGGG ATGCCCCTGC AGAGCAGATG 2810