EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-29158 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr22:47144910-47147620 
Target genes
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GFI1MA0038.2chr22:47146497-47146509TGCAGTGATTTC-6.74
JUND(var.2)MA0492.1chr22:47145695-47145710GATTACCTCATTTTA-6.02
ZNF263MA0528.1chr22:47147178-47147199CTTCCTCCTCCCTCCTTCTCC-6.68
ZNF263MA0528.1chr22:47147193-47147214TTCTCCAGCTCTTCTTCCTCC-6.74
ZNF263MA0528.1chr22:47147175-47147196CTCCTTCCTCCTCCCTCCTTC-6.78
ZNF263MA0528.1chr22:47147171-47147192CTTCCTCCTTCCTCCTCCCTC-6.82
ZNF263MA0528.1chr22:47147161-47147182CTCTCCCCTGCTTCCTCCTTC-7.08
ZNF263MA0528.1chr22:47147158-47147179TCCCTCTCCCCTGCTTCCTCC-7
ZNF263MA0528.1chr22:47147205-47147226TCTTCCTCCTTCCTCTCCTCC-8.21
ZNF263MA0528.1chr22:47147208-47147229TCCTCCTTCCTCTCCTCCTCA-8.31
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_09349chr22:47144642-47146146CD14
SE_09349chr22:47146611-47155259CD14
SE_14697chr22:47144264-47146714CD4_Memory_Primary_7pool
SE_17674chr22:47143988-47146667CD4p_CD25-_CD45RAp_Naive
SE_17901chr22:47143964-47147106CD4p_CD25-_CD45ROp_Memory
SE_18695chr22:47144222-47146665CD4p_CD25-_Il17-_PMAstim_Th
SE_19505chr22:47144496-47147106CD4p_CD25-_Il17p_PMAstim_Th17
SE_20325chr22:47144278-47146904CD56
SE_23520chr22:47145642-47147839Colon_Crypt_1
SE_24287chr22:47145756-47147832Colon_Crypt_2
SE_27442chr22:47144546-47147395Esophagus
SE_28432chr22:47144830-47147523Fetal_Intestine
SE_29215chr22:47144680-47147544Fetal_Intestine_Large
SE_31641chr22:47144513-47147527Gastric
SE_38281chr22:47144111-47147905HUVEC
SE_40789chr22:47146281-47151406Left_Ventricle
SE_42260chr22:47143628-47151410Lung
SE_48916chr22:47146130-47148345Right_Atrium
SE_50233chr22:47144229-47151380Sigmoid_Colon
SE_51682chr22:47146652-47147838Skeletal_Muscle
SE_52427chr22:47144299-47147958Small_Intestine
SE_53517chr22:47144622-47151886Spleen
SE_58383chr22:47122081-47199614Ly1
SE_62483chr22:47129710-47188820Tonsil
SE_65427chr22:47146494-47147656Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr224714524547145535
chr224714580647146214
Number: 1             
IDChromosomeStartEnd
GH22I046748chr224714409547151296
Enhancer Sequence
TCTAGCTCTG TCTTAAATAT ATTGCTAGTT TCTAGGCCTC AGTTTGCCCA CCCACAAAAT 60
GGGAGTATTG GAGGCAGGAA TCTAAGGTGC CCACCTGCTC TCATACTCCA AGGCTCCTTG 120
GGCACATCCT GAGTCCGCCG TTTCCCACAG ACACAGCCGA CTGCCTGCTG CTTTCTCTGT 180
ACGTTTTGTG ACTTCCCTGG GAGCAACATG GAGGAAGGGC CAAGTTTTGA GGTACACAGA 240
GCTTGCTTTA TCTCATGAAG GAAAAAAAGT TCCATGCTTT AATCTTCCTC TTCCAGTAAA 300
GAAACAGCCT GAAGTGGCCT GTCTGCGAGT CACAGTGTTA ACTCAGATCC ACAGGAAGAT 360
GTTCACCGGA TGCTCCTTGG CCAGGCTGCC ATCATCCACT CGGGGGTAAA CAGTCTCCGA 420
ATCAGGGCTG GCTGGCGGCT GACAGCCAGG GCAGGAAGTC TGCAGGGCAA GCTGCAGGAT 480
GTCACCCGAA GGAAATATTT TGTGTTGTGC ATTGCGGTGG AGAAGTGCAA TGAGGCTTAG 540
GGGTTGTGAA AACAGATTCC TCAAGCCTTC ACGGAGGACC TCTGTGCTGG AGGTCTCACC 600
CAACAGGTCT TGCAGGCTGG TCTCAGAGAA GTTCCTAGAG CTGCGTGTGG AGTCACCCAG 660
CCTTCTCCCC CATTCAATAC GGATCCCAGA CATTTGTGGG ATACTTGCAT CTCCCTATAG 720
CACTTTCCCA TGTATCGTCT CATCTGATCT TTAGAAGAAC CCTCCTAGGC ATGCAGGACA 780
GTGCTGATTA CCTCATTTTA CAGATGGGAA GGTGATGCTC AGAGAGGGGG CTGGGATGTG 840
TCCATGTCAC ATGGAATTGG GGCCAACTGA CCCTTGGCCA GCTCTTTGGC TGCATGTGGC 900
ATTTCCAGAT TTCCAGTGGG TGATATGAGG CTTGTGACTC AGAGGGGTGC CCCAGAGATG 960
AAGGGAGAGG AGGCGTGGGG CAGCTCTGGG GTAACTGCCT TGCAGGGGAT GAAGGGAGAG 1020
GAGGCGTGGG GCAGCTCTGG GGAAACTGAC TCGCAGGGGT GCCCCGGAGA TGAAGGGAGA 1080
AGAGGCGTGG GGCAGCTCTG GGGTAACTGC CTTGCAGGGG ATGAAGGGAG AAGAGGCGTG 1140
GGCCAGCTCT GGGGAAACTA ACTCTCAGGA TGTGCGTCAG GGGCTTTCCC AGGCGTCCAG 1200
TGGCATCCAG CATGGTATGG GGCTAGGGTC ATGGGGGCAG GGCGTCAGGA GGCTGGCACT 1260
CCTGCCGTGG GTGGATGGCA TGAGGAAAGG AGGCTTCAGG CATCTTCCTG CATGGGAGAA 1320
ACAACGCCTA GTCCCTTAAC AAGTCCCTGA ATCCTTCAGC TGCTAGCACT CCCCAGCCCA 1380
TTGTCTGTGC CCACTAGAGC CCGTGTGGGT GGTGATTCTG CCCTGTAGGA GCTCCCCATG 1440
GGAGTGGAGG GGAAAGGCCA AGTTCCCCAA AGACAATGTC AGTTTATACT CAGGGAGGGG 1500
CCCACAGGAG GTAGCAGGCC CTGGAATCTG GGGGCTGGAA GTCTGGAGCT GGGCGTGGGG 1560
TGAGGTGTTT GCCTGGGCCT CAAAGCATGC AGTGATTTCA GTGAGTGAGG GTGCAGGGTG 1620
AGGGACGGCT CCCAGGCAGA GGGCACCAGC AACAGACACG CTGGAGTGTG TTGAGGGACA 1680
GAGTACTGGG CAGTGGCAAA AGAGGAGCCC CCAACCTGGA GAGGCCTTGG GTACCAGAGT 1740
GAGGAGTCCG CCGTTTCCCA CAGACACAGG CAGCCCCTGA TGGCTCTTGA GCAGAATGTT 1800
TTACGATGGG AGGTGCTGGG CAGCAGTCAT TGGGGAGGGC CATGGGGAGA GGCCAGCAGG 1860
GGACCAGGGC CCCCTCTCTT GGCTCTAACA GCCCCGCTGT GCCATGGGCA GGATGCCTGG 1920
CAGGTCCAAT TCCAGGCATG GCCGAGGCCA GCAGCCATGG AAGAGTGTCT GGGGTCAGTG 1980
GCTGACAGGA GTGAACGAGG AAACGAGGAA ATGGGGCAGG GCGGGGAGGG CGTGGCACGC 2040
ACTCCACCAG GCCCCAACAG GTGCCCAGTC TGCCACGCAC CCCTGGCCTT GGCCTGGTGC 2100
CTGATAGCTG CCCCTGCTAG GACATGGGGG TGTCGCCCAG CTCTGACAGC TCTGGGAATG 2160
AATCCTGGGC TAAGAGCCAC GAGTCCTCTT CAGGGTTCAG CTGCTCCGCT GAGGCTTAAA 2220
CCAAAAGGTC ATCAGCTCCC GTTCAGCCTC CCTCTCCCCT GCTTCCTCCT TCCTCCTCCC 2280
TCCTTCTCCA GCTCTTCTTC CTCCTTCCTC TCCTCCTCAG GCTCCCTCCC TTCTCCCTTG 2340
ATCTTTAGAA GAATCCTGGG AGAGGGGCAG GACAGTGGCA GTTATCTCCC TCTGACACAG 2400
GGGGAAGGTG AGACCCAGAG AGGGGCTGGG ACTTACCCAG GCCACTTTCC CTGCTCCCTG 2460
CTTCCCACGC CATACCAAAT CACACTGCGC ACTGGGAACA GTATACACGA GAACCTTGGG 2520
CCCTCCTAAG TGGAGCTGCT TTTCCTAGAA TTGCCATCAA CATTTCTAAA CAATGTGGCC 2580
CATCTGGGGG CAAAGCCTCC TCCTTTGGGA ATGACCCCTG CCACAGTGAG GGCCTGACCC 2640
TTTGCAGACC ATTGCAGTCC GCTGGCTTGA CTCTGCCTTC TGGCAACAGA GCTGGGGGAA 2700
GGCCCAGGAA 2710