EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS048-00851 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:31217810-31219990 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6MA0463.2chr1:31219238-31219254AGTTCCTGGAAAGTAC-6.19
BCL6BMA0731.1chr1:31219236-31219253GTAGTTCCTGGAAAGTA-6.23
MSCMA0665.1chr1:31219225-31219235AACAGCTGTT+6.02
MSCMA0665.1chr1:31219225-31219235AACAGCTGTT-6.02
MYF6MA0667.1chr1:31219225-31219235AACAGCTGTT+6.02
MYF6MA0667.1chr1:31219225-31219235AACAGCTGTT-6.02
USF2MA0526.2chr1:31218769-31218785CTGTGTCACGTGGCCC+6.09
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_09454chr1:31213287-31232169CD14
SE_10168chr1:31213284-31236569CD19_Primary
SE_10991chr1:31200236-31237145CD20
SE_12025chr1:31215434-31231414CD3
SE_13126chr1:31218331-31219095CD34_Primary_RO01480
SE_13496chr1:31216473-31219638CD34_Primary_RO01536
SE_13496chr1:31219744-31222092CD34_Primary_RO01536
SE_14586chr1:31213183-31237364CD4_Memory_Primary_7pool
SE_15642chr1:31215491-31224480CD4_Memory_Primary_8pool
SE_16057chr1:31215807-31224418CD4_Naive_Primary_7pool
SE_16511chr1:31215659-31219428CD4_Naive_Primary_8pool
SE_17022chr1:31215376-31224586CD4p_CD225int_CD127p_Tmem
SE_17372chr1:31209247-31236610CD4p_CD25-_CD45RAp_Naive
SE_17902chr1:31209743-31235259CD4p_CD25-_CD45ROp_Memory
SE_18435chr1:31206875-31235130CD4p_CD25-_Il17-_PMAstim_Th
SE_19221chr1:31212331-31225831CD4p_CD25-_Il17p_PMAstim_Th17
SE_20090chr1:31213732-31235754CD56
SE_20783chr1:31215526-31235927CD8_Memory_7pool
SE_21654chr1:31215580-31224503CD8_Naive_7pool
SE_22073chr1:31215463-31231671CD8_Naive_8pool
SE_22484chr1:31213283-31234726CD8_primiary
SE_31319chr1:31215798-31220519Fetal_Thymus
SE_32510chr1:31215436-31239752GM12878
SE_43662chr1:31214270-31233570MM1S
SE_50449chr1:31215714-31235694Sigmoid_Colon
SE_53612chr1:31215423-31231885Spleen
SE_55204chr1:31216087-31220346Thymus
SE_59019chr1:31215557-31239184Ly3
SE_60258chr1:31215621-31235310Ly4
SE_60651chr1:31202709-31239413DHL6
SE_61144chr1:31205054-31253025HBL1
SE_62248chr1:31201545-31253778Tonsil
SE_67247chr1:31214270-31233570MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr13121800331218600
chr13121860031218736
chr13121810731218539
chr13121924231219338
Enhancer Sequence
TGGAAAAATT TAGAAATTTT AATATTGTCC TCCTGAGGCC ATGAGGTCAC CTTGGACATT 60
ACCCGACTTT AGAGACCTCT ACTAATCCTC AACTCCCCCT ACAACTCCTC TGTTCTCCTC 120
CAAGCATCCC TTACTGCCCT GTAACCCCTC CAATCACCCC AGGGGAAGAA GGGGACATTT 180
GTACAGCCTA ACTCCATGCC ACATGATCTT CCCCACTACC CAGAAAAGGG ACTATTCTTA 240
ATACTTTCCT TCCCATTTCA CAGACGAAGA AAGTGCAGCT CAGAGAGGTC CAGGGCCTTG 300
CCCAAGGCCT CCCAGCTGGT CATATGCAGG GCTAGGGTTC AAATCTTGGC CAATTCCCTC 360
CGCTGCCCGG CATCTTCCAG CCACCCGGGC TCTGCCTAAG GCCTAACCCT TCCCCTCAGT 420
GCCTCAGTGG AGGCAGAGAG GCGCCCCCAT CCCCTCTCCC TCTGCAGTCC CCCCTCCCTC 480
CCCTCAGCCC CAGCACCAGG CACCAGAGGT ATTTCTACTT TTGTGAAAAC CACCTGCATT 540
TAAAACCCAG GCTCACCCTC CCCCATTTCA CCTTTTCTCA ACAACCCTGC GGCAGGGGAC 600
GAGGGAGGAC TTTGTCCCCA TTGCCGGATG GCTCACGAGA CTCATAGAGG GCAGGGGACC 660
AGCCCACAGT CACAGAGCGA GGCAACCTCA GAGCCTGACT TAGACTCTGA GGGGCCCCGA 720
CCTTCCACGA AGATGCCAGG CCCTGACCCA GGAGAAAGGG AGGAAGCTCG GCTCTCCAGG 780
CACCCATGTG GCTCTCTAGG ACATAGGATG GAGAGGAACT CACATTTATT CAGCACCTAC 840
TGTGTGCTCA GACCTGCACG CACAGGCTTG CACTGCAATC TCCCAAAACT TTACAAGACA 900
GGCAACATTT TCCCGTTTTA CAGATGAGGA AATGGAGGCT GAGAGAGAAC TCACATGTCC 960
TGTGTCACGT GGCCCGGCTG GGGTGTGAAC CCTGTTGCCT CTCTCCTGGG GTCAGGGCTC 1020
CCCACAAGGT TGAACTTGCT CCCCTGAGGC TCCAGGATCT CTCTAGCCAT CTGCCCACCC 1080
TTCCCTGGCA ACCAAGCCCC AGCCCCAGCC ACTCAGAGCT CAGGAGACAA GAGCTGGGGA 1140
GCAGGAGGCC TCCTCCACTG CCTCACTGCT GTGTGGCCCT GGCCAGGTTC TGGCTTCTCC 1200
CTGGCCTCAG CTTTCGATTC TGGTCAATGA GAAGAGACCC TCATTTTCCC CTGGGGCCAT 1260
TGGGATGACA GAACGCAGGA GGGTCAGTGG GGTGGAGCTC CTACACACTG TAGGACATCT 1320
CACCCAGGCT GCCCACAGTC CTCCACCCCC AGCCACCCCA GGGCCAGCAC CCTGCCCCTC 1380
AGAAGGCCCT CACTGCCCCA CCCATGTCCC TAACCAACAG CTGTTGGTAG TTCCTGGAAA 1440
GTACCTGGCC GACCTACAGA GTATGCAGAC AGTCAACATT TCCAAGCCTC CAAGCCCTTG 1500
CCTTCCCCTC ATGTCCCCGG TTTCCACCTG GACACAGCGC TGCCTTCTCC CCAAGCTCTG 1560
AGAGCCCAGC TGGGCTGTGA CCTTGGGACC CGAGCCATCC CATGACAGGT ACAAGGCTTC 1620
TCTCCCCCAA CAATGCGCAG GCAGACAGCA TGCCCTCACC CACTTGCTCC CCAATTACAG 1680
CATCTTTTCA CCCACTGTCC CTTCATTCTA TGCTGGTGAG ATCATGAAGA TAAGAGCTCG 1740
GGTGCTGGGG TCAGATGGCC CCAGGCCCCA GCCGAGCTCT GCACCCTTGA GCCAGCCACT 1800
AACCTCTCTG GGCCTCGGCT CCTCATCTGA GGAATGGGGA TAATCACTGA CCTGCCTCAC 1860
AGGATTGCTG AGGTCAAATG GAATCGTGTG GTGCGCGGAG CCGGGCACAC AGCAGGTGCA 1920
CCATAAACAA GCACAATTGG GTGGTGGTTT TTGCTACCTC TGGGCATTCA CTGACTCTCA 1980
GTAAACACTC TCTGAGCACC TACCGCCTCC AAACTCTGTC TAGAAAAGCC ACTGACCCTG 2040
GCGTGCCGGT GTCACAGTCT CCAGGGAACT CGATACATGA ATGGTGTGCT CAGAGCCATG 2100
ACAGAGGACA CGCATGGGGC TTGGGGTCCT TGATGAGGGA GAGCGCATTG CTGTCTAAAA 2160
AACTTAGGGA GAATTTCACC 2180