EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS130-18892 
Organism
Homo sapiens 
Tissue/cell
MDA-MB-231 
Coordinate
chr4:10115530-10117730 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6MA0463.2chr4:10116379-10116395CGGCTTTCTAGGAATC+6.87
KLF14MA0740.1chr4:10117609-10117623GAGGGGGCGTGGCG-6.28
KLF16MA0741.1chr4:10117611-10117622GGGGGCGTGGC-6.62
PBX1MA0070.1chr4:10116731-10116743GCATCAATCAAA+6.32
SP3MA0746.2chr4:10117610-10117623AGGGGGCGTGGCG-6.82
SP8MA0747.1chr4:10117610-10117622AGGGGGCGTGGC-6.92
SPICMA0687.1chr4:10117035-10117049TGCTTCCTGTTTTT-6
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_01734chr4:10115764-10118561Aorta
SE_02758chr4:10116522-10118498Astrocytes
SE_04459chr4:10115514-10118183Brain_Anterior_Caudate
SE_05471chr4:10116532-10119955Brain_Cingulate_Gyrus
SE_08364chr4:10116063-10118051Brain_Inferior_Temporal_Lobe
SE_09623chr4:10114621-10120741CD14
SE_12329chr4:10117297-10118067CD3
SE_14886chr4:10116769-10120864CD4_Memory_Primary_7pool
SE_16236chr4:10116827-10120999CD4_Naive_Primary_7pool
SE_17168chr4:10116550-10120562CD4p_CD225int_CD127p_Tmem
SE_17601chr4:10114889-10126849CD4p_CD25-_CD45RAp_Naive
SE_18041chr4:10114662-10121218CD4p_CD25-_CD45ROp_Memory
SE_18604chr4:10090926-10121361CD4p_CD25-_Il17-_PMAstim_Th
SE_19188chr4:10115095-10120578CD4p_CD25-_Il17p_PMAstim_Th17
SE_21402chr4:10116230-10120367CD8_Memory_7pool
SE_22779chr4:10115919-10118581CD8_primiary
SE_23672chr4:10116381-10120266Colon_Crypt_1
SE_24384chr4:10116641-10120117Colon_Crypt_2
SE_26123chr4:10116045-10120882Duodenum_Smooth_Muscle
SE_27018chr4:10116322-10121117Esophagus
SE_30028chr4:10116946-10118234Fetal_Muscle
SE_32010chr4:10116541-10120433Gastric
SE_37776chr4:10116140-10119896HSMMtube
SE_38833chr4:10115045-10120109HUVEC
SE_39084chr4:10116274-10118476IMR90
SE_41136chr4:10116270-10120034Left_Ventricle
SE_42597chr4:10116137-10118617Lung
SE_45147chr4:10116298-10118154NHLF
SE_48189chr4:10116071-10119846Psoas_Muscle
SE_48835chr4:10116297-10118603Right_Atrium
SE_50444chr4:10116206-10121732Sigmoid_Colon
SE_51167chr4:10114584-10120461Skeletal_Muscle
SE_52707chr4:10116274-10118625Small_Intestine
SE_55072chr4:10116777-10121661Stomach_Smooth_Muscle
SE_66345chr4:10117182-10117874Jurkat
SE_69074chr4:10116185-10118650H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr41011680110117310
Number: 1             
IDChromosomeStartEnd
GH04I010113chr41011499310115663
Enhancer Sequence
TGTTGAGTCT GAGATGTCAA TGAGACATGT TAGATCTTCC ATGATCTGGT CCTCCATTTC 60
TTCCCTCTTC CCTCCCTGAG CCTGCATTCC AAACAGACCA TCATCCTTCC TGAACGGTCA 120
TGCCAATTCA TGTCACTTTT TTTTCCAAGA GTACTTTGCC CTAAAAAAAA TCGTACCCAC 180
CTTTACTTGA GTACCCAGTC CACCCATCCA ACTAACAAGA GACTCAGTGC CTGATCTACA 240
TCCAGCCCAG GGAGGGCTAT ATTAGTAGCA TCTCGTGCTG ACCTGGCATT GCAGAAACTT 300
AAAAATAATT GAGAAGGGAA ACAGGGTAAC CCCTGAGAAG AAAATGGCAA ACCACGGGGA 360
AGGGGTAAGA ATACAGAGCT CAGAAACAGG CAGAATGGGT TTCACAAGCT GGGAAATGCT 420
TTCTGCAAAG GGGTGCCTGT CCCTGAATGA CCACTCCATT AGAAGCAGCT CCAGTTACTG 480
GCCTGCCTCA CCTTGCTAAG TCTGACTCCT CTTTAGAGTA ACGGACCCAT GTGGGGTGGA 540
AAGAGATGCT ACAGTTTAAG AAGCTATCAC AGGGCCAGAT GCACAGCAGG TACTTTATGT 600
GAGGCCCCCT CCCTGGAAGT CAATGTGGAC TGCAACGACA GGGAAGGCCT GGTTAGGGGC 660
AAAACGAAAT ATCCTACTGC TCTGTATCCG AGGACGTGTT AGTGGATTTT ATTTGCCAAA 720
CTACTAAATA TCTCTTTAGG GTTGTCTCAA TTTTTATTTT CTCAAAAGCC TCAGGACCTG 780
CCTTCGGAGA CTTCCAGATC ATTACCATTA GATCCCTGGT GATTTTCTCC AGTTCTAAGC 840
AAGGCCCTTC GGCTTTCTAG GAATCTGTGT GACTAGCAAG TTGTTAGCAC CTTCAAAGCA 900
CATTCACACC CGCCCACCCC CTCATTTGAG GGGCCCAGCA ATCCAGGGCA GGTAGAGCTC 960
TGTCTTCCAG CAGAGGAACA GCAGCGACTG CCTGGGTTAA CGAGACAGAT GCGGGCAGAG 1020
CCAGCAGCTC TTCGGACCAA GAGGCTTCTC CTTTCACAGA GAAGGAAACT GAGACCCAGA 1080
GACCCCTTCA TTCCCTCAGC CAGTTGCTGG CCTCCTGGAG GGCAAGTGTG TCCGATCAAC 1140
AGTCCCAACC TACCAAGGGA AATCAGGCTG ACTTTAAGTT GACAACCCTT GTATGCCTAT 1200
GGCATCAATC AAAACATACA TCTTTGTGCC AGCCGCCCCC ACTAAGCACA GCACAGGAGA 1260
AATCACCCAA TGGCCGGGCC GGCACCTCCA ACTCCCACCC CACCAATTCC ATCACTCAGG 1320
CTGAGGAAGG GAAAAGCAAA ATTTAAGCGT GTAACCCAGG AAGGGAGGGA GACTGACAGA 1380
CTGGGTCACC CCAACAATTA CAGAGGAATA ACATGAATTT GCAAGGATTT CCCAAGGAGC 1440
TGGCTCTAGA AGCCTTTTCA GCCTGGGTAC CGGAGGCTTG CAGAGAATGA TTCATGGGAA 1500
AACACTGCTT CCTGTTTTTG CTTTGGGGCT TAGATCCATG GTGGCAGATC TGGCTGGCCC 1560
AGAGGCCCGG GTGTTTTTCC GGGCTCTGCC ATACTGGAAG ACCAGGGTAT TAACAGCGAG 1620
TTAGCTGAGT GCCATTCCAT TCAGCAAGGG CTCAAAGTGC ACCAGGCACC GCTGGGCTTG 1680
AGGGACGCCA GCAGCTCATT CATTCCATCT GCCCAGCCAG CAGGCGAAGC GAGAGTGGTC 1740
ATCATCTCAT CATCTGTTTT ACAGACGAGA AAACTGGGGC TCAGAGATGC CCAAATCGCC 1800
AATCTTCTCA AGGTCACGCA GCGGCCGACC GGGTCAGTCT GATCCCTCAA ATCCGGAGCC 1860
CTTGCTTTTA AGGAATGAAC TAATCTAATC TCCCATCCAC GTACTAACCA GGCCTGACCG 1920
TGCTTAGCTT CCAAGATCAG AGGCGATCCG GCGCTTTCAG GGTGCTATGA CCGTAGACAG 1980
AAACGAACTA AGACTCAGTT TCCTCATCAA GAAGGAGCAG ACAAGGACCT GGGTGAATCT 2040
GAGGCCGGCT TCCGGGGCTC CGAGGTGTGG CTCCCGGTAG AGGGGGCGTG GCGCCCTCAC 2100
CCTCCCCGGG CCAATGGGCA GGAGGTGAGA AGTGGAGAGG AAGGCGAATT ATCCCATCCC 2160
AAGGTGGCTC CGGAGCAGAA CCGCGCCCGG GGTAGGGGGT 2200