EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-20233 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr22:47145220-47148030 
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GFI1MA0038.2chr22:47146497-47146509TGCAGTGATTTC-6.74
JUND(var.2)MA0492.1chr22:47145695-47145710GATTACCTCATTTTA-6.02
RELAMA0107.1chr22:47147762-47147772GGAAATTCCC-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: 3             
ChromosomeStartEnd
chr224714524547145535
chr224714580647146214
chr224714768347147890
Number: 1             
IDChromosomeStartEnd
GH22I046748chr224714409547151296
Enhancer Sequence
GAAGTGGCCT GTCTGCGAGT CACAGTGTTA ACTCAGATCC ACAGGAAGAT GTTCACCGGA 60
TGCTCCTTGG CCAGGCTGCC ATCATCCACT CGGGGGTAAA CAGTCTCCGA ATCAGGGCTG 120
GCTGGCGGCT GACAGCCAGG GCAGGAAGTC TGCAGGGCAA GCTGCAGGAT GTCACCCGAA 180
GGAAATATTT TGTGTTGTGC ATTGCGGTGG AGAAGTGCAA TGAGGCTTAG GGGTTGTGAA 240
AACAGATTCC TCAAGCCTTC ACGGAGGACC TCTGTGCTGG AGGTCTCACC CAACAGGTCT 300
TGCAGGCTGG TCTCAGAGAA GTTCCTAGAG CTGCGTGTGG AGTCACCCAG CCTTCTCCCC 360
CATTCAATAC GGATCCCAGA CATTTGTGGG ATACTTGCAT CTCCCTATAG CACTTTCCCA 420
TGTATCGTCT CATCTGATCT TTAGAAGAAC CCTCCTAGGC ATGCAGGACA GTGCTGATTA 480
CCTCATTTTA CAGATGGGAA GGTGATGCTC AGAGAGGGGG CTGGGATGTG TCCATGTCAC 540
ATGGAATTGG GGCCAACTGA CCCTTGGCCA GCTCTTTGGC TGCATGTGGC ATTTCCAGAT 600
TTCCAGTGGG TGATATGAGG CTTGTGACTC AGAGGGGTGC CCCAGAGATG AAGGGAGAGG 660
AGGCGTGGGG CAGCTCTGGG GTAACTGCCT TGCAGGGGAT GAAGGGAGAG GAGGCGTGGG 720
GCAGCTCTGG GGAAACTGAC TCGCAGGGGT GCCCCGGAGA TGAAGGGAGA AGAGGCGTGG 780
GGCAGCTCTG GGGTAACTGC CTTGCAGGGG ATGAAGGGAG AAGAGGCGTG GGCCAGCTCT 840
GGGGAAACTA ACTCTCAGGA TGTGCGTCAG GGGCTTTCCC AGGCGTCCAG TGGCATCCAG 900
CATGGTATGG GGCTAGGGTC ATGGGGGCAG GGCGTCAGGA GGCTGGCACT CCTGCCGTGG 960
GTGGATGGCA TGAGGAAAGG AGGCTTCAGG CATCTTCCTG CATGGGAGAA ACAACGCCTA 1020
GTCCCTTAAC AAGTCCCTGA ATCCTTCAGC TGCTAGCACT CCCCAGCCCA TTGTCTGTGC 1080
CCACTAGAGC CCGTGTGGGT GGTGATTCTG CCCTGTAGGA GCTCCCCATG GGAGTGGAGG 1140
GGAAAGGCCA AGTTCCCCAA AGACAATGTC AGTTTATACT CAGGGAGGGG CCCACAGGAG 1200
GTAGCAGGCC CTGGAATCTG GGGGCTGGAA GTCTGGAGCT GGGCGTGGGG TGAGGTGTTT 1260
GCCTGGGCCT CAAAGCATGC AGTGATTTCA GTGAGTGAGG GTGCAGGGTG AGGGACGGCT 1320
CCCAGGCAGA GGGCACCAGC AACAGACACG CTGGAGTGTG TTGAGGGACA GAGTACTGGG 1380
CAGTGGCAAA AGAGGAGCCC CCAACCTGGA GAGGCCTTGG GTACCAGAGT GAGGAGTCCG 1440
CCGTTTCCCA CAGACACAGG CAGCCCCTGA TGGCTCTTGA GCAGAATGTT TTACGATGGG 1500
AGGTGCTGGG CAGCAGTCAT TGGGGAGGGC CATGGGGAGA GGCCAGCAGG GGACCAGGGC 1560
CCCCTCTCTT GGCTCTAACA GCCCCGCTGT GCCATGGGCA GGATGCCTGG CAGGTCCAAT 1620
TCCAGGCATG GCCGAGGCCA GCAGCCATGG AAGAGTGTCT GGGGTCAGTG GCTGACAGGA 1680
GTGAACGAGG AAACGAGGAA ATGGGGCAGG GCGGGGAGGG CGTGGCACGC ACTCCACCAG 1740
GCCCCAACAG GTGCCCAGTC TGCCACGCAC CCCTGGCCTT GGCCTGGTGC CTGATAGCTG 1800
CCCCTGCTAG GACATGGGGG TGTCGCCCAG CTCTGACAGC TCTGGGAATG AATCCTGGGC 1860
TAAGAGCCAC GAGTCCTCTT CAGGGTTCAG CTGCTCCGCT GAGGCTTAAA CCAAAAGGTC 1920
ATCAGCTCCC GTTCAGCCTC CCTCTCCCCT GCTTCCTCCT TCCTCCTCCC TCCTTCTCCA 1980
GCTCTTCTTC CTCCTTCCTC TCCTCCTCAG GCTCCCTCCC TTCTCCCTTG ATCTTTAGAA 2040
GAATCCTGGG AGAGGGGCAG GACAGTGGCA GTTATCTCCC TCTGACACAG GGGGAAGGTG 2100
AGACCCAGAG AGGGGCTGGG ACTTACCCAG GCCACTTTCC CTGCTCCCTG CTTCCCACGC 2160
CATACCAAAT CACACTGCGC ACTGGGAACA GTATACACGA GAACCTTGGG CCCTCCTAAG 2220
TGGAGCTGCT TTTCCTAGAA TTGCCATCAA CATTTCTAAA CAATGTGGCC CATCTGGGGG 2280
CAAAGCCTCC TCCTTTGGGA ATGACCCCTG CCACAGTGAG GGCCTGACCC TTTGCAGACC 2340
ATTGCAGTCC GCTGGCTTGA CTCTGCCTTC TGGCAACAGA GCTGGGGGAA GGCCCAGGAA 2400
GGATCAAGAG GGTTCCAGGC CCTGGAGCCC TATCTCCCCA CTTCCCTCAG GTTACATCCA 2460
GTGCACTTGC CAAGTATGTC ATCAATGACC AAGTGAGGAC CCCGGGAAGC TCGGTGGGGA 2520
AGGCGGGGGG CTATGACCTA CTGGAAATTC CCATAGCCAG AGTGATGGGG ATGAAGGAGA 2580
GGTGCTGGTT TGGGACACAG CCTGCTGCAG GGACTCGCAG AGCCAAGGAC AGAGCAGAGC 2640
AGGCATGGCA GGCGGTGTGA GGACCCGGCC CTGGCAGCTG GGAGGGTGCC TGGATGATGG 2700
TCCCCCTGCT GGAGACCCCC TCTCTTGCCT GTCTCAGTTG GCCTGGGCTT TGTCCTCCGC 2760
TGACCAACAC CCTCCACACA TTGCTTGACA CTCACAGTGG GGAGGTGTCC 2810