EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS044-05672 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr17:38698030-38700310 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RFX2MA0600.2chr17:38699070-38699086AGTTCCCATGGAAACG-6.06
TCF3MA0522.2chr17:38698108-38698118AGCAGGTGTT-6.02
ZNF263MA0528.1chr17:38698539-38698560CTCCCCCTCCTTTCCGCCTCC-6.32
Number of super-enhancer constituents: 52             
IDCoordinateTissue/cell
SE_00517chr17:38687646-38700726Adipose_Nuclei
SE_00798chr17:38698005-38698497Adipose_Tissue
SE_01363chr17:38696079-38700112Adrenal_Gland
SE_02998chr17:38697429-38700114Bladder
SE_03777chr17:38698044-38698792Brain_Angular_Gyrus
SE_06594chr17:38696184-38700427Brain_Hippocampus_Middle
SE_08685chr17:38697766-38699954Brain_Inferior_Temporal_Lobe
SE_10931chr17:38696534-38700426CD20
SE_12200chr17:38696282-38699352CD3
SE_14639chr17:38696043-38699986CD4_Memory_Primary_7pool
SE_16947chr17:38696413-38699287CD4p_CD225int_CD127p_Tmem
SE_17295chr17:38695285-38699870CD4p_CD25-_CD45RAp_Naive
SE_17919chr17:38695762-38700313CD4p_CD25-_CD45ROp_Memory
SE_18283chr17:38695786-38700667CD4p_CD25-_Il17-_PMAstim_Th
SE_19186chr17:38695615-38700360CD4p_CD25-_Il17p_PMAstim_Th17
SE_20639chr17:38694387-38700386CD56
SE_20960chr17:38695933-38700003CD8_Memory_7pool
SE_21909chr17:38695980-38699596CD8_Naive_8pool
SE_22423chr17:38696028-38698879CD8_primiary
SE_25403chr17:38691460-38700381DND41
SE_25943chr17:38691615-38700599Duodenum_Smooth_Muscle
SE_26577chr17:38695474-38700326Esophagus
SE_29882chr17:38697403-38700604Fetal_Muscle
SE_31181chr17:38694605-38700325Fetal_Thymus
SE_32359chr17:38696450-38700283Gastric
SE_35821chr17:38697585-38700292HMEC
SE_37372chr17:38697904-38700552HSMMtube
SE_38887chr17:38696233-38700332IMR90
SE_41480chr17:38693853-38700350Left_Ventricle
SE_42403chr17:38688893-38700340Lung
SE_44181chr17:38697136-38700351NHDF-Ad
SE_44928chr17:38697958-38700201NHLF
SE_45551chr17:38687599-38700884Osteoblasts
SE_46930chr17:38697620-38700272Ovary
SE_47885chr17:38697952-38698590Pancreas
SE_47885chr17:38699322-38699689Pancreas
SE_48754chr17:38694072-38700335Right_Atrium
SE_50356chr17:38695576-38700335Sigmoid_Colon
SE_51567chr17:38691551-38700708Skeletal_Muscle
SE_51937chr17:38698102-38700248Skeletal_Muscle_Myoblast
SE_52624chr17:38693869-38700302Small_Intestine
SE_53520chr17:38688782-38700318Spleen
SE_54860chr17:38691653-38700606Stomach_Smooth_Muscle
SE_55173chr17:38695466-38700190Thymus
SE_56221chr17:38698121-38700059u87
SE_58835chr17:38672665-38782311Ly3
SE_61067chr17:38687460-38781557HBL1
SE_61495chr17:38672564-38757231Toledo
SE_62232chr17:38671160-38782171Tonsil
SE_63720chr17:38698056-38700229HSMM
SE_64249chr17:38698592-38700071NHEK
SE_67770chr17:38698121-38700059u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr173869872138700000
chr173869920538699580
chr173870000038700103
Number: 1             
IDChromosomeStartEnd
GH17I040528chr173868498238700734
Enhancer Sequence
GTAACAACAG CCAGGCTCTG GCAGTCGCAC TTTCACACCG GAGTCCTCAC CTCGCCCACA 60
GTGCCCTGGA AGCATGAGAG CAGGTGTTAT TGTTGAGGGC ACTGAGAAAG AGAGAGAGAG 120
GGGCCAAAGA GCTAGTTCAA AGGCATCCCG GTTCTCACTC TGGCCTCAGA CTCCCCTTCT 180
GGGGTCCTTG AGGGCCCCTA GGCCACCCCG AGGGGTTGGA GGAACACTTT GTCCATTCCC 240
CGTGGCAGAT GGAAGGACTC CGGAGCATGT CAGCTGCAGC CTGGGCCTCT GTTGGGTCCT 300
CGGCTCTGGG TCTCTCACAG GCGGCCATCA AGGTGTTGGC TGGGGCCTTG GTCATCTCAA 360
GGCTGGAGCA GGAAAGGACC TGCCTCCCCA GGCCCTAAGC TTGAATGGTG CTGGGGACAG 420
GGGGCAGCAC TCTTCTGGCA CGGCAGCCCC TCCTCCGTCC TCTTGGCATC TTGTCCTTAA 480
AGTTCATCGT TGCCTCGTCC GCTAACCTCC TCCCCCTCCT TTCCGCCTCC ATCTCCCCAA 540
GTCCTTCTCG CCTCTGCTTT TGCTTCCACG GCTGTTTCCT CACGGAGGCT CAGACAATAG 600
AGGCTAATGA TCCAACTGCT GAGAGCACAC CCTCCTCTAG CAGCCAGAAA TCATCTGTTA 660
CCCATCGCCC GCCCTCCCTG GGGCCCAGGC TTCCAGACTG AGACCTTTTC CTTCCCTCCC 720
ACTTCTTACT GGAAATGAGC CCCCGTCCTT CCACTCCCCC CTAACCCCCC AGGCCTCCCT 780
TAGGGAGGTT CAAGGACTCG TCTCTGACTC CACCTATCTA CTGGGTACCC CTCTGCAGGG 840
GGGAGGCAGG GGCTGGTGCC CACGAACTCT GGAGGCCCTT CTGGGAGCAC AGTCTTGCCA 900
TGACCTCTCT AGGTCAGCTC AGCTCCCTGT GCTGGACACA GACCCGGAGA ACAGCTCAGC 960
ACGAGGTTAC CAGGCTGACG TTGCACAGAC TGTGCTGGAA ATTACAGAGT GCCTTGGAGG 1020
GAAAAACAAA CTGGGGTTTC AGTTCCCATG GAAACGACAT CTATTTGCAG AGGTGCTTGC 1080
GTCAGAGCCC GGGACCCTGT GCTTGGCAGG GATGGGGTGG ATGTTAAAAG GCAGGGTCAT 1140
CTGTTGACTG TCTGGGACTC TTCCAGGACA GTGTCTGAAA TGGGGCCCTT ACCTTTAGCC 1200
ATGACAAACA GCTCTTTCCA CAGAGGGGCC TGTCTGCCTG GGCATGTCTC TGCAATGCTG 1260
GGGTTTTTGG GTAGATTTTA AACTTATGAG TCAAGGGTGT GGGAAGACCC CACATTCGCC 1320
ATTCATGAGC ATTTATTCCA CGAGCATGTT TTGACCTATG ATGTGCCAGG CACTGGGCTA 1380
GGCCAGCCAA TCAGGAGTTG GTCTGGACCT GCTAAGTTTG GGGCCTAAAG TCTCCCTTCC 1440
TGGGAGGAGC TTTGGTCAGA CAGGGGCAAA GTGGGGACCT GCCAGGGACC ACGTGACGTG 1500
GGAGCACACA GGCTCAGCAA TGCCAGTCCC CTCACTCTGT AACCAAAGCA AATGCCTTCT 1560
GTCCTCGTGT GTCACAGGGG AGTAATTCCT CATCTCACGG GGAAAGATGA CCCCTAAACT 1620
AGCCACTGAG GTCCCCACAG CAGAGGCGAT TATTCCAGCT ATTGTTATGG AAGAGTGTCT 1680
ATTGTTACCC TCTCTATCAC TTTACACTTT ACGAAGAGCT GTACATCCAC TACCTCGTTT 1740
AATGTAACAC TCCAGGGAGG TTTTAACAAC ATCACACCTG TTTTCAAACG GGGAAACTGC 1800
ATCGAGGGAG GAGAAGGCAC TTGTCAAGGT CACACGGATG ATAAACGGTG AGACCAGTAT 1860
GGGAATCTGA ATGCCGGACC CCCTGCTTTG CCCCCTCCTC CCTGTCCTGG GGCACCTGGT 1920
GACCAGACCT CCCACCCTGG CAGGCCTCCA ACCAGCCCGG CTGTTTCCCA CGCCTGGGGA 1980
ATGGGAACCA GCTGTGTGCT AGTGCGGTGG GGCATGGATT GTTCTGGATC TGGTCTCATG 2040
GAGACTGCAC ATCAGAAAGA CCACAACCCT CAACTCTGCT GCTCACCCAA GTCACTTCAC 2100
TCTTCCTTGA CTCAGTTTCC CTCTCAGTAA GTTGACAGAA AGCCTGTGAG GGGATCTGAG 2160
TGACTTATGT CCTATAAGAA ATCTGAAGAA ATAGGCCGGG CGCAGTGGCT CACGCCTGTA 2220
ATCTCAGCAC CTTGGGAGGC TGAGGTGGGC GGATCATGAG GTCAGGAGTT TGACAGCAGC 2280