EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS148-07472 
Organism
Homo sapiens 
Tissue/cell
NHLF 
Coordinate
chr17:43389200-43390940 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr17:43390904-43390919AGGTCTCTCTGACCT-6.44
IRF1MA0050.2chr17:43389690-43389711TGCTGGTTTCATTTTCATCTG+6.11
RREB1MA0073.1chr17:43390672-43390692CCACCAAACACCACCAACAA+6.95
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_01249chr17:43388149-43389866Adrenal_Gland
SE_01249chr17:43389876-43391126Adrenal_Gland
SE_04602chr17:43387681-43391078Brain_Anterior_Caudate
SE_11470chr17:43370585-43396257CD20
SE_15206chr17:43388386-43397109CD4_Memory_Primary_7pool
SE_18500chr17:43387479-43397228CD4p_CD25-_Il17-_PMAstim_Th
SE_19630chr17:43387582-43396207CD4p_CD25-_Il17p_PMAstim_Th17
SE_23493chr17:43387582-43391120Colon_Crypt_1
SE_24167chr17:43388391-43390604Colon_Crypt_2
SE_24167chr17:43390739-43391078Colon_Crypt_2
SE_25878chr17:43387248-43395764Duodenum_Smooth_Muscle
SE_26725chr17:43387623-43393334Esophagus
SE_30018chr17:43387566-43390933Fetal_Muscle
SE_31611chr17:43388205-43391255Gastric
SE_32589chr17:43387754-43395497GM12878
SE_34075chr17:43387678-43390986HCC1954
SE_40748chr17:43387552-43395549Left_Ventricle
SE_41691chr17:43388360-43389804LNCaP
SE_41691chr17:43389960-43390580LNCaP
SE_43331chr17:43387609-43395776Lung
SE_44657chr17:43388788-43394471NHDF-Ad
SE_46201chr17:43388243-43399699Osteoblasts
SE_47195chr17:43387470-43394435Panc1
SE_48714chr17:43387602-43391213Right_Atrium
SE_49545chr17:43388257-43389771Right_Ventricle
SE_49545chr17:43389907-43390514Right_Ventricle
SE_49545chr17:43390553-43391051Right_Ventricle
SE_50169chr17:43387586-43397347Sigmoid_Colon
SE_51970chr17:43388168-43390648Skeletal_Muscle_Myoblast
SE_52792chr17:43387582-43397353Small_Intestine
SE_59053chr17:43370566-43412054Ly3
SE_62481chr17:43366079-43396493Tonsil
SE_63770chr17:43387668-43391131HSMM
SE_65719chr17:43388051-43391087Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr174338947543389771
Enhancer Sequence
CCCCAGGGCC AAAGCTCCCC TCCTGCTTCT TTGCTGACTG TCACTGGAAG CAGGCCATTT 60
TCCACCCTCA GGGTGGCTGG ACTTAGGAGT CAGTGACACT GCTGATCTGG GCTCTGTGCC 120
CCGTCCACGA TCCCCCCTCC GCTGTCAGCC CACTGGCCCC AGAAGCCTCC TGTTTACCTC 180
CTGCCCCCTG CCTCCATAGC CCTGGGGCTG GGATGAGGCT GATTTGTGGC AGAGGGCTCC 240
TCACGAAGGT CTGCTCAGGA CTTTCTCTGC AACTGTGCTG GGGAATAAAT CGCCTGTCAC 300
CTACACCCCT GCATGGGTGA CTCACCTTCC AGAGAAAGTG CTCTGCTCAC CTAAGCAAAG 360
CTGCTTGGAA AATGACTAAG GCACCTATCA AATGCACTCT GTGGGGCCAA CCAGTTATGG 420
AGCAAGGTCC AGGCACACTC TGCCTCTCAC CTCCAGCCTG AAGTCAAGTG CAGAGCTGCC 480
ACGCCAGGCC TGCTGGTTTC ATTTTCATCT GAACCGAGCT CCACATGAGG CTTGACATCC 540
GGTGATCTAT TTTTTCTAAA AACTAGCTTC ACTTTAGAAA TGACTCTTCG GCCATCAAGT 600
CAGCTTCCCC AAGAGAAAAC AAAATGTTAT TTAAAGGGAA CAGTAGCCTG GTGAGAGCCT 660
ATATTTTTGT TTTGTATTAA GGTGAAAAAA GACTTTAAAA TATAACATGA AACTTTTTTT 720
TTCCCTTGTG AGATTAAAAC AAACGTTTTT CTTTCAAGAG ATGGGGTCTC GCTATGTTGC 780
CCATAGCTAC TTGACCTCCT GGGCTCAAGT GATCCTCCCG CCTCAGCCTC TCAAGTAGCT 840
GGGACTAAAG AAACACACGT CACCATTCCA GGCTTCTTGT GAGATTTAAA GGGGAATCTG 900
CAAGTCCTTG ACTGCAGATC GTGGGCCCCC AGACAGAGTC TCAGAGAGAA GCTGACAAAG 960
ACATCTTTAC GAGGGGGAAA GGGTGGTGAG CTGGGGATGC CATGTGGTAG TGGGAACCTC 1020
ATCCCACAGA ACCAAATGTT CCCTCCTGTT CCCCCAAAGA ACAAGTCCTT GCTGATCTAC 1080
ATGCCATACA GTATTTTCCC TTTCCTCACC TCCAGGATTA ATGCAGGAAC CTACTTGATC 1140
ACGTGTGGGA CACAGGAAGC CCCTAGACAG GCCTAGCTGT GTCTCCAGCT CAGAGTTAGG 1200
ATTGTCAACT GGGCAGAGCC TGGACCTTTG TAGCCTCATT TGGAGTATGG TGAGGGCAGT 1260
ATATAGTGTA AGACAGGGAG AACCCGAGAG CTGAAGCTTT TAGACTGAAG GACTGTCCCC 1320
CTAAAGGTCC TACTGAGAAA ATGACTCTGG CCTGTCAGGC AGTCTGACCC TTCTTGACAT 1380
CATCTTACAG AAAACAGGTT TAGTCACAAT GCAGTAATTG GCAACTACTA CTGCTACTAT 1440
TACTACTACT ACTACTACTA CTATTACTAC CACCACCAAA CACCACCAAC AAGAACAACA 1500
ACAACAACAA CAACAGTTAC AGCCTCTATG TTCTGTGCTG GGCACTGGGC TCAGCACTTT 1560
ACATATCTCC TCTCATTTTC TACTCAAAAC AGCCCCATGA AGTATTTCTG ATCCCATTCA 1620
CAGATGAGGC ACCTGATGAT TAGAGAAGTG AAGTGATTTG CTTGCGGGCA CACAGGCAGG 1680
CCGTGGCAGA CCTCGACCTG ACCCAGGTCT CTCTGACCTG ACAGCCTCAG CCACCACATG 1740