EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS108-32462 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr5:118606500-118609650 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CrxMA0467.1chr5:118607074-118607085TTAATCCTCTT-6.14
OLIG2MA0678.1chr5:118607905-118607915ACCATATGGT+6.02
OLIG2MA0678.1chr5:118607905-118607915ACCATATGGT-6.02
ZBTB18MA0698.1chr5:118608917-118608930AAGCCAGATGTTC+6.19
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_09224chr5:118603212-118615449CD14
SE_10192chr5:118607088-118608487CD19_Primary
SE_10192chr5:118608683-118615243CD19_Primary
SE_11647chr5:118601731-118629910CD20
SE_11852chr5:118605560-118612730CD3
SE_14409chr5:118603151-118612367CD4_Memory_Primary_7pool
SE_15917chr5:118603495-118608314CD4_Naive_Primary_7pool
SE_15917chr5:118608538-118610338CD4_Naive_Primary_7pool
SE_16877chr5:118607266-118608001CD4p_CD225int_CD127p_Tmem
SE_16877chr5:118608134-118610700CD4p_CD225int_CD127p_Tmem
SE_17336chr5:118602883-118628254CD4p_CD25-_CD45RAp_Naive
SE_17778chr5:118602583-118615257CD4p_CD25-_CD45ROp_Memory
SE_18242chr5:118602749-118628149CD4p_CD25-_Il17-_PMAstim_Th
SE_19112chr5:118603127-118615248CD4p_CD25-_Il17p_PMAstim_Th17
SE_20232chr5:118603110-118616440CD56
SE_20766chr5:118602925-118610958CD8_Memory_7pool
SE_22243chr5:118603037-118612666CD8_Naive_8pool
SE_22350chr5:118602970-118626914CD8_primiary
SE_25388chr5:118602919-118611945DND41
SE_30942chr5:118603373-118612790Fetal_Thymus
SE_39376chr5:118604403-118611507Jurkat
SE_50308chr5:118606481-118612025Sigmoid_Colon
SE_55141chr5:118607343-118608158Thymus
SE_55141chr5:118608685-118609683Thymus
SE_58310chr5:118603634-118704575Ly1
SE_59637chr5:118603673-118697862Ly4
SE_61019chr5:118608552-118705688HBL1
SE_62209chr5:118603018-118707327Tonsil
SE_66260chr5:118604403-118611507Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5118608388118609042
Enhancer Sequence
TAATCTAGAT TATGTGATGA TTTAAGAATT ATTAATAAAT CAGTGAATAA AACAAGGTTC 60
TACCAAAAGC ATAGTGATCC TGCACAAATG GGCCTTTTAA ACACTTTCTT TAAGGGCAAC 120
TTTTACTCCG TGTACCTTTT GTTCCAGTGT GTTTAAACTC ACCAAGAAAA GTTGGTGTGA 180
GTTGAGAAAT CTCATGTTTG TTGTCTCTTA ATTTTCTATT TCAGACTATA TTGCTAGACA 240
TAGTCTTTGT TTACGTGTTG AGCTGTCGTG AGGACAGGCT GTCCTGGGAT CCTAAACAGA 300
ATAGCAGAAA CCTGGGGGTG AACACACTGC AGAGGCCAGG AACAGAGTAT TTTATGAGGC 360
CAGTTCTTTG CAATTCTCAT TCTGTTGAAA TGGAGGAAAG GGTGTGTGGA GAGGAATGAT 420
TGCATCCAAA CAGTACTAAT TAGGAAATGC TGAGTTGGGG GAGGAGTGGA TTTCTATGTG 480
ACTTACGGCT TGGAGAACTT CACAGAGGTG ATCTTTAAAG TTGAGTCTGC CACAGTGCCA 540
GGCACTGCAG AGGTCTCATA TTTAATTGAT CCAATTAATC CTCTTTTGCA GAAGATAGCC 600
CAATGTGGTA GTAACACCCT TCCTGGAGAT TTCATTCATT CTCAGAATTG AGCTTTGATC 660
TACCTCATGT AGAATGGTCC ATTCCTCACT GCCTCCATTT ATGCGTGATA GCAGTTGAAG 720
GGGCTGAAAA TGGGATAACC TCCAGGAGAC GGGAGAAGCA GTGATGATAA ATAAGGGCCA 780
CCTGCTTTTT CACAGAGGGG AAGGGCATAG GGGCTATTAG TACAATTCCA GTGCCAGGGG 840
CATTGACTTT GGCAATGGCG ACATGCACAG GGGCCAATCT GGATAACAAA GTGGACAATT 900
TTCCCTGCTT TGGCATTCTC AGGGATCTCT GGCTCTGATA CAGAAGTTAA GGGAAGGAGT 960
TGTGTGGTGC CAGATTAACT TTTATCACCT CACCCCTCCT CACACTGCCC ACATCCTGCA 1020
TTTAATACCA AATGCACACA GCAAGAACTC AACAAACACT GAAAAGGCCC TCGTAACACC 1080
CAACCTTTAT GTTTCCCTCT GGCTAAGAAT TTTCTTCCCA TACTCTTGTC TCTGGTTTTG 1140
ATGACTGTGG CCCTGGAGTC TGAGCCAACT GCAGTTTCTA GGCTTCTATA CTTCAGTTGT 1200
GCTGCCCAGT AGCTGAAAAT GAATAATTTG TAGAGGGTAA AAAACAAAAA CAGAGAACCA 1260
TGTTGCAAAA TGTAAAGGAG GTCAGTTCAT TTTTAGCCTA CATTTTGGCC TGAAGAGGAG 1320
GAAATGAGCT ACAAGTGGAG GGTAGATAAT TCTAGAATAG CAGAGCCAAG GGGTATCTTG 1380
GAAACCACCT GGTCTATGGC CTTACACCAT ATGGTTGCTA TTCCTCAACT TTGGAGGTGT 1440
CCATCTCCTT AAGTCCAGCT TGCAGGAGGA GAGCACCATT CATTCACACA GCAGGCATTT 1500
ATTGAGCTCC TGCTATGTGC CTGGTACAGC ACACCCTTCT CATGTTTACA TGAAATCCTT 1560
GGGATTTGAG AAGGCAGGTA ACTTGCGTAA AGATGTCTGT TGATAAGAAG GAGTCCCTGA 1620
AGGTAAGTTG CTAGTGGCAA AAATGGGTTT GGAATTCTGT TGTGTTTCAC AAGGGCAGTA 1680
GAATGATATT CAAAATATTT GTCTTTCTCA ACAATAAGAA ACTCAAAAGA AGCACATTTC 1740
TGCCAACATC TGTTTCAAAT AACCAGTGGT ATTACTGAAA CAAACCTGAT TCCATAGGAT 1800
TTTGTTTTAC ATCAGACATA AGTTACCTGA GAATTGTTTG AAAATGTCAC AGGCTCAGCA 1860
ATAATCAAAT AATACCCAGC CCATCCTTTT AGACAGCAGT TGTTTTTTCT CTGGAAGCAA 1920
GTGTTTATGG TTCAGAACTA AGGTAGCTGA GGTTCAGAAC CAGCTGCAAA GCTGGGTGTG 1980
TGCCAAAAAG GTTGTTTTCC TAGGCTTGCC CTTTTCCGTA TAGGACAAGG GGGATTAAAA 2040
ACCAACATGG TGATGTTTCT GTCAAGGTGA CGGGGGGCTA GGTGTACAGA TCTTTTCCAC 2100
TAAAAACAAG GGTTGCGGGC AGGTGGTCAC AGGATTGAGA CTCCAGGCTA ACTCGTAAAC 2160
ACCTCTGGGT TCGTTTCTTT AATAACAGAA TGGAATTAAG TTCAAAATTC CACTTGTAGT 2220
TTCCTTAAAC ATTGGGAATA AAGATGACTT TAGTCAAGAA GTAGTTGGTC CAAATGACTT 2280
TGCTGGAATC AGCAGCTCAT GTCTCAGCCC CTGCTGGCTG TGTGGCTTTG GACAATCTAC 2340
TTAGCTCTCT GAGCCTGTTT CTTCACCAGA GTAAAAACTG GGGATAGTAT TTATATTATA 2400
GGATTGTTGT GCAGATTAAG CCAGATGTTC CTCTCCTGTA TCAGTGTGCA GAAGGCACCC 2460
ATTAAGTGGA GGACTTAGTT AGATTGGCCA AATAGGTCTC ATTCCAGTAA GTGTTAGTAC 2520
TGAGCCACAG TGGAGTAGAG AGGGAAAGTA GTAACTTGTG TCATATGTGA TTTTAGCATG 2580
AATTCTTTTT TCCTTTAACA ATGCCAGAGG AGCCCAGAGA ATGGGGTGAA TGTAGCACAA 2640
CTTCAGTGAT TGCTAGCTGC AGGGTCACAT GATTATATAA GGGAAATGTC ACCGCTGCTG 2700
CCAAAGATAA GTGAGCCAGA GCAGGGCATT CGAGTTTTAT GTGCCTGAGA ACGAAGACGA 2760
GCCATAGTAC CCATTAAGCT TCTCTGCATG AGGGAAGCTT TCAAAAGACC TATTACAGTT 2820
AAATTGTGAG CAGTGGGTTG GCCTTTCACA ACTCCCATGT TTAAAACAGG TAGTGAATGA 2880
AACCAGATTA TTTAAGACAG ACAGCTGCCC TTGGTGTTGC AAAGGGAATC GGGCTGGCAT 2940
GTCTTCAGGG GAAGTTGCGT GAGGTCCGGG AGGCCCAGGG CAGGGACCGC ATCTGCAGGA 3000
TTAGGCACCG GGGCAAGGTC TTTTGGGAAC ACAGTACTCA GCAAGGCACA CAGTAGACTC 3060
TTGGATATTT TAAAGGAGCC AAAAAGTAAG CAACAGCTCA CTCTGTCAAT ACCCTCTCTA 3120
AGCCTGGCTC TTACTCCTTC AACCCAAATT 3150